HUMAN ARTIFICIAL CHROMOSOME VECTOR

Abstract

A human artificial chromosome vector comprising a human antibody heavy chain gene, a human antibody light chain gene, and a human antibody surrogate light chain gene.

Description

TECHNICAL FIELD

The present invention relates to a human artificial chromosome vector comprising a human antibody heavy chain gene, a human antibody light chain gene, and a human antibody surrogate light chain gene, an animal having the human artificial chromosome vector, and a method for producing a human antibody.

BACKGROUND ART

The development of a technology of producing a chimeric animal by fusing micronuclei comprising human chromosome fragments with cells having pluripotent differentiation to obtain hybrid cells allows to prepare a non-human animal maintaining large exogenous genes to be produced (Non-Patent Document 1 and Patent Document 1).

Subsequently, a method for constructing a desired human artificial chromosome (hereinafter abbreviated to HAC) vector to produce the non-human animal has been proposed, by which the HAC including a wide range of human antibody gene loci has been established.

First, as a method for modifying a chromosome fragment to be introduced into a non-human animal, a technology of preparing a deleted chromosome with a high efficiency by inserting a telomere sequence into a desired sequence on a human chromosome kept in a chicken DT40 cell by gene targeting has been developed (Patent Document 2).

Further, in a process of maintaining a mouse cell keeping a human chromosome, it has been found that a fragment SC20 comprising an antibody heavy chain gene locus derived from the human chromosome 14 may be obtained, and the fragment is stably maintained in an embryonic stem (ES) cell and an individual of the mouse and has high transmission efficiency to progeny (Patent Document 2).

Therefore, a λHAC comprising a human antibody heavy chain and a human λ chain was constructed by translocating a fragment comprising the antibody λ type light chain gene locus on the human chromosome 22 through the Cre/loxP site specific recombination system using such SC20 as a basic skeleton of a vector (Non-Patent Document 2 and Patent Document 3).

The λHAC has the stability and transmission efficiency to progeny almost equivalent to the SC20 and a chimeric mouse which stably maintains a λHAC was produced by introducing the_λHAC into the mouse ES cells (Non-Patent Document 2 and Patent Document 3). It is now possible to construct a HAC vector including a human chromosome region having a specific megabase (Mb) size by the method.

Further, for the purpose of removing chromosome regions which adversely affect the generation of a chromosome-introduced animal, chromosome fragments ΔHAC and ΔΔHAC with an optimal size including the antibody λ type light chain (λ chain) gene region were prepared (Patent Document 4), based on the structural information of the human chromosome 22 (Non-Patent Document 3).

It was confirmed that the ΔHAC and ΔΔHAC include regions having 2.5 Mb and 1.5 Mb sizes, respectively, which are shorter than the periphery of the antibody λ type light chain gene region on the λHAC, 10 Mb, to impart a transmission efficiency to progeny higher than that of the λHAC (Patent Document 4).

Meanwhile, human polyclonal antibodies currently used for treatment and prevention of various diseases are prepared from a serum pool obtained from a plurality of human donors. For this reason, the performance of the human polyclonal antibodies depends largely on human donor sera as a supplying source, and thus a process of selecting a donor having a desired antigen reactivity or titer is required in preparing.

In addition, due to factors such as the kind of antigen, the number of exposure to an immunogen, and the amount of donor serum which may be collected, in preparing a polyclonal antibody; the development of the use thereof is limited. Therefore, a transgenic animal having a human antibody gene locus as a means for producing human polyclonal antibodies has been prepared.

Due to its body size, an ungulate animal is useful as a source of supplying a large quantity of human polyclonal antibodies. So far, in order to produce human polyclonal antibodies, a bovine into which the above-described HAC, specifically ΔHAC and ΔΔHAC are introduced to produce human polyclonal antibodies, is known (Non-Patent Document 4 and Patent Document 5).

In the neonatal sera of the bovine into which these HACs were introduced, 13 to 258 ng/mL of the human immunoglobulin (Ig) G was produced (Non-Patent Document 4).

Subsequently, in order to eliminate bovine antibodies produced in a bovine living body, gene targeting was carried out on IGHM and IGHML1 encoding the functional IgM genes among bovine endogenous antibody heavy chain genes and as a result, a bovine in which antibody heavy chains were knockout was known (Non-Patent Documents 5 and 6 and Patent Documents 6 and 7).

When ΔΔHAC was introduced into the obtained antibody heavy chain double-knockout bovine (IgHM^−/−IgHML1^−/− bovine), it was found 7.1 μg/mL of a human IgG was produced in a serum of a 14-day-old calf (Patent Document 7).

In addition, a bovine into which κHAC which is a HAC vector having a human antibody heavy chain gene locus and a human antibody κ type light chain (κ chain) gene locus was introduced was produced (Non-Patent Document 6 and Patent Document 8). κHAC is a vector constructed by translocating a fragment comprising the antibody κ chain gene locus on the human chromosome 2 onto the SC20. In FIG. 1, a schematic view of κHAC is shown.

Among IgHM^−/−/IgHML1^−/− bovines into which κHAC was introduced, clone 468 which was the highest antibody producing individual constantly produced a human IgG at 1 g/L or more in the serum from the 84 days after birth, and exhibited a titer exceeding 2 g/L at the 210 days after birth.

However, a technology of stably producing an individual which exhibits high titer as described above has not been known, and thus there is a need for animals which produce human antibodies with higher efficiency or a technology which can stably produce these animals.

CITATION LIST

Patent Document

Patent Document 1: WO97/07671

Patent Document 2: WO98/37757

Patent Document 3: WO00/10383

Patent Document 4: WO02/92812

Patent Document 5: WO2002/70648

Patent Document 6: WO03/97812

Patent Document 7: WO05/104835

Patent Document 8: WO09/111086

Non-Patent Document

Non-Patent Document 1: Tomizuka et al., Nature Genetics, 16, 133-143, 1997

Non-Patent Document 2: Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000

Non-Patent Document 3: Dunham et al., Nature, 402, 489-495, 1999

Non-Patent Document 4: Kuroiwa et al., Nature Biotechnology, 20, 889-894, 2002

Non-Patent Document 5: Kuroiwa et al., Nature Genetics, 36, 775-780, 2004

Non-Patent Document 6: Kuroiwa et al., Nature Biotechnology, 27, 173-181, 2009

SUMMARY OF INVENTION

Technical Problem

It is an object of the present invention to provide an animal for producing human antibodies efficiently, a method for stably supplying the animal, and a method for producing human antibodies with high efficiency.

Solution to Problems

Considering the above object, the present inventors modified the HAC vector for the purpose of achieving high production amount of the human IgG and stably producing a bovine individual with a high titer, compared to the conventional HAC.

That is, the present invention relates to the following (1) to (8).

(1) A human artificial chromosome vector comprising a human antibody heavy chain gene, a human antibody light chain gene, and a human antibody surrogate light chain gene.

(2) The human artificial chromosome vector described in (1), in which the human antibody surrogate light chain gene is VpreB gene and λ5 gene.

(3) The human artificial chromosome vector described in (1) or (2), comprising a gene of a non-human animal-derived IgM heavy chain constant region.

(4) The human artificial chromosome vector described in (3), in which the gene of the non-human animal-derived IgM heavy chain constant region is derived from bovine IGHM.

(5) An animal having the human artificial chromosome vector described in (1) or (2).

(6) A bovine having the human artificial chromosome vector described in (3) or (4).

(7) A method for producing a human antibody, comprising: administering a target antigen into an animal described in (5) to produce and accumulate the human antibody specific to the antigen in serum of the animal, and recovering the human antibody specific to the antigen from the serum.

(8) A method for producing a human antibody, comprising: administering a target antigen into a bovine described in (6) to produce and accumulate the human antibody in serum of the bovine, and recovering the human antibody specific to the antigen from the serum.

Advantageous Effects of the Invention

Human antibodies may be produced with high efficiency by introducing the HAC vector comprising the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene of the present invention into an animal as compared to the vector produced by the conventional HAC technology. In addition, an animal which is capable of producing a human antibody with high efficiency may be stably produced by introducing the human artificial chromosome vector of the present invention into an animal.

Furthermore, as a preferred embodiment, when a human artificial chromosome vector which further comprises a gene of a non-human animal-derived IgM heavy chain constant region in addition to the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene is introduced into an animal, a human antibody may be produced with a further higher efficiency, and an animal which is capable of producing a human antibody with such high efficiency may be stably produced.

BRIEF DESCRIPTION OF THE DRAWINGS

[FIG. 1] FIG. 1(a) illustrates a schematic view of κHAC. FIG. 1(b) illustrates a schematic view of an IgM to be formed on a B cell membrane when κHAC is introduced into an animal. In FIG. 1(b), the dotted-line represents a human-derived IgM part, and the solid-line represents a bovine-derived IgM part.

[FIG. 2] FIG. 2(a) illustrates a schematic view of KSL-HAC. FIG. 2(b) illustrates a schematic view of an IgM to be formed on the B cell membrane when KSL-HAC is introduced into an animal. In FIG. 2(b), the dotted-line represents a human-derived IgM part, and the solid-line represents a bovine-derived IgM part.

[FIG. 3] FIG. 3(a) illustrates a schematic view of cKSL-HACΔ. FIG. 3(b) illustrates a schematic view of an IgM to be formed on the B cell membrane when cKSL-HACΔ is introduced into an animal. In FIG. 3(b), the dotted-line represents a human-derived IgM part, and the solid-line represents a bovine-derived IgM part.

[FIG. 4] FIG. 4 illustrates a schematic view of a targeting vector pTEL'hisDpuro^lox2272F9R9.

[FIG. 5] FIG. 5 illustrates a schematic view of a targeting vector pTELCAGzeoSLF2R2.

[FIG. 6] FIG. 6 illustrates a schematic view of a targeting vector p553CAG^lox2272BsrDT.

[FIG. 7] FIG. 7 illustrates a schematic view of a targeting vector pSC355CAG^lox511hisDDT.

[FIG. 8] FIG. 8 illustrates a schematic view of a targeting vector p14CEN(FR)hygpuro^lox511DT.

[FIG. 9] FIG. 9 illustrates a schematic view of a targeting vector pRNR2^loxPbsrDT.

[FIG. 10] FIG. 10 illustrates a schematic view of a targeting vector pCH2CAGzeoDT.

[FIG. 11] FIG. 11 illustrates an outline of a method for modifying the human chromosome 2 in a chicken DT40 cell.

[FIG. 12] FIG. 12 illustrates an outline of a method for modifying the human chromosome 22 in a chicken DT40 cell.

[FIG. 13] FIG. 13 illustrates an outline of a method for constructing the SLKH fragment in a DT40 hybrid cell.

[FIG. 14] FIG. 14 is a view illustrating an outline of a method for constructing KSL-HAC in a DT40 hybrid cell.

[FIG. 15] FIG. 15 illustrates an outline of a method for constructing the CH2D fragment in a DT40 hybrid cell.

[FIG. 16] FIG. 16 illustrates an outline of a method for modifying the human chromosome 14 in a DT40 hybrid cell.

[FIG. 17] FIG. 17 illustrates an outline of a method for constructing cKSL-HACΔ in a DT40 hybrid cell.

[FIG. 18] FIG. 18 illustrates a total amount of the human IgG in each serum of 6-month-old HAC bovines.

[FIG. 19] FIG. 19 illustrates the result of a CEM cell specific ELISA assay.

EMBODIMENTS FOR CARRYING OUT THE INVENTION

The present invention relates to (1) a human artificial chromosome vector comprising a human antibody heavy chain gene, a human antibody light chain gene, and a human antibody surrogate light chain gene, (2) an animal having the human artificial chromosome vector, and (3) a method for producing a human antibody, comprising administering a target antigen into the animal to produce and accumulate the antigen-specific human antibody in the serum of the animal, and recovering the antigen-specific human antibody from the serum.

1. The Human Artificial Chromosome Vector of the Present Invention

In the present invention, “the human artificial chromosome vector” refers to a vector which comprises a human chromosome-derived centromere sequence, a telomere sequence, and a replication origin and exists independently from a chromosome of a host cell in a nucleus of the host cell.

Specifically, the vector refers to a human artificial chromosome (HAC) vector prepared by translocating a desired region on the human chromosome into a stable human chromosome fragment.

Specific examples of a method for preparing a HAC include a method comprising: inserting a telomere sequence and a sequence loxP recognized by a Cre recombinant enzyme such that a desired region on a human chromosome or a chromosome fragment may be included, and binding a region inserted between the telomere sequence of the chromosome or the chromosome fragment and the loxP sequence to a region inserted between a telomere sequence on another chromosome or chromosome fragment (preferably a chromosome fragment which is stable in the nucleus and has a high transmission efficiency to progeny) and the loxP sequence by translocation (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and WO No. 00/10383).

(Human Antibody Heavy Chain Gene)

The human artificial chromosome vector of the present invention comprises a human antibody heavy chain gene. In the present invention, “the human antibody heavy chain gene” refers to a gene which, among two identical heavy chains and two identical light chains constituting a human immunoglobulin molecule, encodes the former.

Specific examples of the human antibody heavy chain gene include a gene encoding a variable region of the human antibody heavy chain and genes encoding the γ chain, μ chain, α chain, δ chain, and ε chain, ands chain which determine the structure of the constant region.

It is preferred that the artificial chromosome vector of the present invention comprises a gene encoding a variable region of the human antibody heavy chain and genes encoding the γ chain, μ chain, α chain, δ chain, and ε chain which determine the structure of the constant region, as the human antibody heavy chain gene.

In the artificial chromosome vector of the present invention, “comprising the human antibody heavy chain gene” refers to comprising a DNA encoding the human antibody heavy chain gene. The human artificial chromosome vector of the present invention may be prepared by inserting a DNA encoding the human antibody heavy chain gene into any position or inserting or ligating a chromosome fragment comprising a DNA encoding the human antibody heavy chain gene.

The variable region gene and the constant region gene of the human antibody heavy chain form a cluster and is positioned at 14q32 on the human chromosome 14. Therefore, the artificial chromosome vector of the present invention preferably comprises a human chromosome 14, more preferably a human chromosome 14 at which the variable region gene and the constant region gene of the human antibody heavy chain are positioned, and further preferably a human chromosome 14 comprising the 14q32 region.

(Human Antibody Light Chain Gene)

The human artificial chromosome vector of the present invention comprises a human antibody light chain gene. In the present invention, “the human antibody light chain gene” refers to a gene that, among two identical heavy chains and two identical light chains constituting a human immunoglobulin molecule, encodes the latter.

Specific examples of the human antibody light chain gene include two types of genes, i.e., the κ chain gene and the λ chain gene. The gene of each chain comprises a gene encoding a variable region and a gene encoding a constant region.

The human artificial chromosome vector of the present invention may comprise either κ chain gene or the λ chain gene only, or both of the genes as the human antibody light chain gene.

In the human artificial chromosome vector of the present invention, “comprising the human antibody light chain gene” refers to comprising a DNA encoding the human antibody light chain gene. The human artificial chromosome vector of the present invention may be prepared by inserting a DNA encoding the human antibody light chain gene into any position or inserting or ligating a chromosome fragment comprising a DNA encoding the human antibody light chain gene.

Each of the variable region gene and constant region of the κ chain and the λ chain forms a cluster to be positioned on a chromosome. The κ chain gene cluster is positioned at 2p11.2-12 of the human chromosome 2 (Gottfrie et al., Genomics, 16. 512-514, 1993) and the λ chain gene cluster is positioned at 22q11.2 of the human chromosome 22 (Collins et al., Nature, 377, 367-379, 1995).

Therefore, the artificial chromosome vector of the present invention preferably comprises a human chromosome 2 fragment, more preferably a human chromosome 2 fragment at which the κ chain gene cluster is positioned, and even more preferably a human chromosome 2 fragment comprising the 2p11.2-12 region.

In addition, the artificial chromosome vector of the present invention preferably comprises a human chromosome 22 fragment, more preferably a human chromosome 22 fragment at which the λ chain gene cluster is positioned, and even more preferably a human chromosome 22 fragment comprising the 22q11.2 region.

(Human Antibody Surrogate Light Chain Gene)

The human artificial chromosome vector of the present invention comprises a human antibody surrogate light chain gene. In the present invention, “the human antibody surrogate light chain gene” refers to a gene encoding an imaginary antibody light chain which is associated with an antibody heavy chain produced by a gene reconstitution in the human pro-B cell to constitute the pre-B cell receptor (preBCR).

Specific examples of the human antibody surrogate light chain gene include the VpreB gene and the λ5 gene. The human artificial chromosome vector of the present invention preferably comprises the VpreB gene and the λ5 gene as a human antibody surrogate light chain gene.

The VpreB gene of the present invention preferably comprises either or both of the VpreB1 gene and the VpreB3 gene and more preferably both of the VpreB1 gene and the VpreB3 gene.

In the human artificial chromosome vector of the present invention, “comprising the human antibody surrogate light chain gene” refers to comprising a DNA encoding the human antibody surrogate light chain gene. The human artificial chromosome vector of the present invention may be prepared by inserting a DNA encoding the human antibody surrogate light chain gene into any position or inserting or ligating a chromosome fragment comprising a DNA encoding the human antibody surrogate light chain gene.

Any of the VpreB gene and the λ5 gene is positioned within the human antibody λ chain gene locus at 22q11.2 of the human chromosome 22. Therefore, the human artificial chromosome vector of the present invention preferably comprises the human chromosome 22, more preferably the human chromosome 22 comprising the VpreB gene and the λ5 gene, and furthermore preferably the human chromosome 22 comprising the 22q11.2 region.

(IgM Heavy Chain Constant Region Gene)

The human artificial chromosome vector of the present invention also preferably comprises a non-human animal-derived IgM heavy chain constant region (μ chain) gene. The non-human animal is not particularly limited so long as the animal is a non-human animal which can be a host into which the human artificial chromosome vector of the present invention is introduced, and may be any of ungulates such as cows, horses, goats, sheep, and pigs; rodents such as mice, rats, and rabbits; poultry such as chickens, domestic ducks, and geese.

The non-human animal is preferably a non-human mammalian animal, more preferably an ungulate animal, and furthermore preferably a bovine.

In the present invention, “the IgM heavy chain constant region gene” refers to a gene encoding the IgM heavy chain constant region. The IgM heavy chain constant region promotes the generation of the B cell by interacting with the B cell membrane molecule Igα/Igβ to cause a signal transduction in cells. Specific examples of the IgM heavy chain constant region gene include genes encoding constant region domains such as CH1, CH2, CH3, and CH4, and the B-cell transmembrane domains such as TM1 and TM2.

The IgM heavy chain constant region gene derived from a non-human animal which is comprised in the human artificial chromosome vector of the present invention is not particularly limited so long as the region is in a range which may sufficiently induce the signal of the B cell generation in the above-described IgM heavy chain constant region, but preferably comprises TM1 domain and TM2 domain derived from a non-human animal, and more preferably genes encoding CH2 domain, CH3 domain, CH4 domain, TM1 domain, and TM2 domain which are derived from a non-human animal.

In the human artificial chromosome vector of the present invention, “comprising the non-human animal-derived IgM heavy chain constant region gene” refers to comprising a DNA encoding a non-human animal-derived IgM heavy chain constant region gene.

The human artificial chromosome vector of the present invention may be prepared by inserting a DNA encoding IgM heavy chain constant region gene derived from a non-human animal into any position, or ligating a chromosome fragment comprising a DNA encoding a human IgM heavy chain constant region gene.

In particular, it is preferred that some of the DNA encoding the human IgM heavy chain constant region gene on the human artificial chromosome is substituted with some of the DNA encoding the non-human animal-derived IgM heavy chain constant region gene.

Specifically, when a part of the DNA encoding the human IgM heavy chain constant region gene on the human artificial chromosome is substituted with a part of the DNA encoding IgM heavy chain constant region gene derived from a non-human animal, the DNAs encoding the TM1 domain and the TM2 domain in the human IgM heavy chain constant region gene on the human artificial chromosome are preferably substituted with the DNAs encoding the TM1 domain and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively; and the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain, respectively, in the human IgM heavy chain constant region gene are more preferably substituted with the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively.

The IgM heavy chain constant region gene derived from a non-human animal is preferably the IgM heavy chain constant region gene of a non-human mammalian animal, more preferably the IgM heavy chain constant region gene of an ungulate animal, and furthermore preferably the IgM heavy chain constant region gene of a bovine.

The IgM heavy chain constant region gene of the bovine is preferably a gene encoding a bovine IgM heavy chain constant region which is included in an IGHM region at which a bovine endogenous IgM heavy chain gene is positioned (derived from IGHM) or a gene encoding a bovine IgM heavy chain constant region in an IGHML1 region (derived from IGHML1), and more preferably a gene encoding a bovine IgM heavy chain constant region which is included in the IGHM region.

2. Method of Constructing a Human Artificial Chromosome Vector of the Present Invention

The human artificial chromosome vector comprising the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene of the present invention may be constructed by using the following (1) to (3) methods.

(1) Construction of a Human Artificial Chromosome Fragment Comprising a Human Antibody Heavy Chain Gene

The human artificial chromosome vector comprising the human antibody heavy chain gene may be constructed by isolating the human chromosome 14 from a human normal cell to obtain a chromosome fragment comprising a human antibody heavy chain gene from the chromosome in accordance with a method described in WO98/037757.

Specifically, although a chromosome fragment which is incidentally generated during an isolation process of the human chromosome 14 or a process of maintaining the chromosome in a cell may be isolated by a method described in WO00/010383, a chromosome fragment may be obtained by irradiating an ionized radiation on the human chromosome 14 to break the chromosome, and a chromosome fragment may be also obtained by inserting a telomere sequence into a desired position of the human chromosome 14 to generate a deletion at the position.

Further, the thus obtained human artificial chromosome vector may be constructed by inserting or ligating a human chromosome fragment which does not comprise the human antibody heavy chain gene into a fragment comprising the human chromosome 14-derived human antibody heavy chain gene by using a method by Kuroiwa et al. (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and WO00/010383).

Examples of the human artificial chromosome fragment comprising the human antibody heavy chain gene include SC20 (Tomizuka et al., Proceeding of the National Academy of Sciences, 97, 722-727, 2000 and WO98/037757), λHAC (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and WO00/010383), κHAC (Kuroiwa et al., Nature Biotechnology, 27, 173-181, 2009 and WO09/111086), ΔHAC and ΔΔHAC (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and WO00/10383), and the like.

(2) Construction of an Artificial Chromosome Fragment Comprising a Human Antibody Light Chain Gene

The human artificial chromosome fragment comprising the human antibody κ chain gene may be constructed by isolating the human chromosome 2 from a human normal cell to obtain a chromosome fragment comprising a human antibody κ chain gene from the chromosome in accordance with a method described in WO98/037757.

Specifically, although a chromosome fragment which is incidentally generated during the isolation process of the human chromosome 2 or the process of maintaining the chromosome in a cell may be isolated by a method described in WO00/010383, a chromosome fragment may be obtained by irradiating an ionized radiation on the human chromosome 2 to break the chromosome, and a chromosome fragment may also be obtained by inserting a telomere sequence into a desired position of the human chromosome 2 to generate a deletion at the position.

A human artificial chromosome fragment comprising the human antibody κ chain gene may be constructed by inserting or ligating a fragment comprising the human antibody κ chain gene derived from the human chromosome 2 into a human chromosome fragment which does not comprise the human antibody κ chain gene derived from the human chromosome 2 by using a method by Kuroiwa et al. (Kuroiwa et al., Nature Biotechnology, 27, 173-181, 2009 and WO09/111086).

Examples of the human artificial chromosome fragment comprising the human antibody κ chain gene to be thus obtained include κHAC (Kuroiwa et al., Nature Biotechnology, 27, 173-181, 2009 and WO09/111086).

The human artificial chromosome fragment comprising the human antibody λ chain gene may be constructed by isolating the human chromosome 22 from a human normal cell to obtain a chromosome fragment comprising a human antibody λ chain gene from the chromosome in accordance with a method described in WO98/037757.

Specifically, although a chromosome fragment which is incidentally generated during the isolation process of the human chromosome 22 or the process of maintaining the chromosome in a cell may be isolated by a method described in WO00/010383, a chromosome fragment may be obtained by irradiating an ionized radiation on the human chromosome 22 to break the chromosome, and a chromosome fragment may also be obtained by inserting a telomere sequence into a desired position of the human chromosome 22 to generate a deletion at the position.

Further, a human artificial chromosome fragment comprising the human antibody λ chain gene may be constructed by inserting or ligating a fragment comprising the human antibody λ chain gene derived from the human chromosome 22 into a human chromosome fragment which does not comprise the human antibody λ chain gene by using a method of Kuroiwa et al. (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and WO00/010383.

Examples of the thus obtained human artificial chromosome fragment comprising the human antibody heavy chain gene include λHAC (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and WO00/010383), ΔHAC and ΔΔHAC (Kuroiwa et al., Nature Biotechnology, 20, 889-894, 2002 and WO02/092812).

(3) Construction of a Human Artificial Chromosome Fragment Comprising a Human Antibody Surrogate Light Chain Gene

The human artificial chromosome fragment comprising the human antibody surrogate light chain gene may be constructed by isolating the human chromosome 22 from a human normal cell to obtain a chromosome fragment comprising a human antibody surrogate light chain gene from the chromosome in accordance with a method described in WO98/037757.

Specifically, although a chromosome fragment which is incidentally generated during the isolation process of the human chromosome 22 or the process of maintaining the chromosome in a cell may be isolated by a method described in WO00/010383, a chromosome fragment may be obtained by irradiating ionized radiation on the human chromosome 22 to break the chromosome, and a chromosome fragment may also be obtained by inserting a telomere sequence into a desired position of the human chromosome 22 to generate a deletion at the position.

Further, a human artificial chromosome fragment comprising the human antibody surrogate light chain gene may be constructed by inserting or ligating a fragment comprising the human antibody surrogate light chain gene into a human chromosome fragment which does not comprise the human antibody surrogate light chain gene by using a method of Kuroiwa et al. (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and WO00/010383.

The human artificial chromosome vector comprising the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene of the present invention may be constructed by ligating a human chromosome 2 fragment comprising the human κ chain gene constructed by the method of (2) and a human chromosome 22 fragment comprising the human λ chain gene and the human antibody surrogate light chain gene constructed by the methods of (2) and (3) into a human chromosome 14 fragment comprising the human antibody heavy chain gene constructed by the method of (1).

More specifically, a human artificial chromosome vector comprising the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene of the present invention may be constructed in the following manner.

First, a loxP sequence and a lox2272 sequence which are recognition sequences of a Cre recombinant enzyme are inserted into the cos138 site (Kuroiwa et al., Nature Biotechnology, 27, 173-181, 2009) which is positioned on the polar centromere side and into the AC104134 site (Gene Accession No.) which is positioned on the polar telomere side of the human κ chain gene cluster region on the human chromosome 2 fragment, respectively, by homologous recombination.

Meanwhile, after a telomere sequence is inserted into the AP000350 site (Gene Accession No.) on the polar telomere side of a cluster region comprising the human λ chain gene and the human antibody surrogate light chain gene on the human chromosome 22 fragment by homologous recombination and then cut the chromosome, the lox 2272 sequence is inserted into the AP000553 site (Gene Accession No.) on the polar centromere side by homologous recombination.

Further, the loxP sequence is introduced into the RNR2 gene locus (Worton et al., Science, 239, 64-68, 1988) on the human chromosome 14 fragment by homologous recombination.

By Cre/loxP recombination, both chromosomes are ligated by translocating the AP000553 site on the human chromosome 22 fragment into the AC 104134 site on the human chromosome 2 fragment.

Further, by Cre/loxP recombination, three chromosomes are ligated by translocating the RNR2 gene locus on the human chromosome 14 fragment into the cos138 site on the human chromosome 2 fragment of the above ligated bodies.

Examples of the thus constructed human artificial chromosome vector of the present invention include KSL-HAC. FIG. 2 illustrates a schematic view of KSL-HAC. As shown in FIG. 2, since KSL-HAC further comprises a gene encoding a human antibody surrogate light chain as compared to the structure of κHAC (FIG. 1), it can produce human antibodies with higher efficiency when it is introduced into an animal. In addition, KSL-HAC may stably produce an animal which is capable of producing a human antibody with such high efficiency.

Furthermore, the human artificial chromosome vector of the present invention comprising a non-human animal-derived IgM constant region gene may be constructed by the following method.

(4) Construction of a Human Artificial Chromosome Vector Comprising a Non-Human Animal-Derived IgM Heavy Chain Constant Region Gene

The non-human animal-derived IgM heavy chain constant region gene may be inserted into a human artificial chromosome fragment by substituting the human IgM heavy chain constant region gene of the human artificial chromosome fragment comprising the human antibody heavy chain gene which is constructed by the method of the above (1) with a non-human animal-derived IgM heavy chain constant region gene.

Specifically, the non-human animal-derived IgM heavy chain constant region gene may be constructed by substituting the DNAs encoding the TM1 domain and the TM2 domain in the human IgM heavy chain constant region gene on the human artificial chromosome fragment comprising the human antibody heavy chain gene constructed by the method of the above (1) with the DNAs encoding the TM1 domain and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively, by homologous recombination; preferably the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain with the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively, by homologous recombination.

Therefore, the human artificial chromosome vector comprising the human antibody heavy chain gene and the human antibody light chain gene and also comprising the non-human animal-derived IgM heavy chain constant region gene may be constructed by substituting the DNAs encoding the TM1 domain and the TM2 domain in the human IgM heavy chain constant region gene on the human artificial chromosome fragment comprising the human antibody heavy chain gene in the human artificial chromosome vector comprising the human antibody heavy chain gene and the human antibody light chain gene constructed by the methods of the above (1) to (3) with the DNAs encoding the TM1 domain and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively, by homologous recombination, preferably the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain with the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively, or the DNAs encoding the CH1 domain, the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain with the DNAs encoding the CH1 domain, the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively, by homologous recombination.

Further, the human artificial chromosome vector comprising the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene of the present invention and also comprising the non-human animal-derived IgM heavy chain constant region gene may be constructed by using the methods of the above (1) to (4).

Specifically, the human artificial chromosome vector comprising the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene as well as the non-human animal-derived IgM heavy chain constant region gene may be constructed by substituting the human IgM heavy chain constant region gene on the human chromosome 14 fragment comprising the human antibody heavy chain gene constructed by the method of (1) with the non-human animal-derived IgM heavy chain constant region gene by the method of (3), and then ligating the human chromosome 2 fragment comprising the human κ chain gene constructed by the method of (2) and the human chromosome 22 fragment comprising the human 2 chain gene and the human antibody surrogate light chain gene constructed by the methods of (2) and (3).

More specifically, a human artificial chromosome vector comprising the human antibody heavy chain gene, the human antibody light chain gene, and the human antibody surrogate light chain gene of the present invention and also comprising the non-human animal-derived IgM heavy chain constant region gene may be constructed in the following manner.

First, the DNAs encoding the TM1 domain and the TM2 domain in the human IgM heavy chain constant region gene on the human chromosome 14 fragment are substituted with the DNAs encoding the TM1 domain and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively, and the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain are preferably substituted with the DNAs encoding the CH2 domain, the CH3 domain, the CH4 domain, the TM1 domain, and the TM2 domain of the non-human IgM heavy chain constant region gene, respectively, by homologous recombination. Subsequently, a loxP sequence is inserted into the RNR2 gene locus (Worton et al., Science, 239, 64-68, 1988) on the human chromosome 14 fragment by homologous recombination.

Meanwhile, a loxP sequence and a lox2272 sequence which are recognition sequences of a Cre recombinant enzyme, are inserted into the cos138 site (Kuroiwa, Nature Biotechnology, 27, 173-181, 2009) which is positioned on the polar centromere side and into the AC104134 site (Gene Accession No.) which is positioned on the polar telomere side of the human κ chain gene cluster region on the human chromosome 2 fragment, respectively, by homologous recombination.

Further, after a telomere sequence is inserted into the AP000350 site (Gene Accession No.) on the polar telomere side of a cluster region comprising the human λ chain gene and the human antibody surrogate light chain gene on the human chromosome 22 fragment by homologous recombination and then cut the chromosome, a lox 2272 sequence is inserted into the AP000553 site (Gene Accession No.) on the polar centromere side by homologous recombination.

By Cre/loxP recombination, both chromosomes are ligated by translocating the AP000553 site on the human chromosome 22 fragment into the AC104134 site on the human chromosome 2 fragment. In addition, by Cre/loxP recombination, three chromosomes are ligated by translocating the RNR2 gene locus on the human chromosome 14 fragment into the cos138 site on the human chromosome 2 fragment of the above ligated bodies.

Examples of the human artificial chromosome vector of the present invention to be constructed in this manner include cKSL-HACΔ. In FIG. 3, a schematic view of cKSL-HACΔ is shown. As shown in FIG. 3, since cKSL-HACΔ further comprises a gene encoding a human antibody surrogate light chain and a non-human animal (bovine)-derived IgM heavy chain constant region gene compared to the structure of κHAC (FIG. 1), it can produce human antibodies with higher efficiency when it is introduced into an animal, and an animal which is capable of producing human antibodies with such a high efficiency may also be stably produced.

3. An Animal Having the Human Artificial Chromosome Vector of the Present Invention

The animal having the human artificial chromosome vector of the present invention refers to an animal into which the human artificial chromosome vector of the present invention is introduced.

The animal having the human artificial chromosome of the present invention is not particularly limited so long as the animal is an animal in which the human artificial chromosome fragment may be introduced into a cell thereof, and any non-human animals, for example, ungulates such as cows, horses, goats, sheep, and pigs; rodents such as mice, rats, and rabbits; poultry such as chickens, domestic ducks, and geese; and the like may be used.

The non-human animal is preferably a non-human mammalian animal, more preferably an ungulate animal, and even more preferably a bovine.

An animal having the human artificial chromosome vector of the present invention may be constructed by introducing the human artificial chromosome vector of the present invention constructed by the method of the above (2) into an oocyte of a host animal.

Specifically, the human artificial chromosome vector of the present invention to be constructed by the method of the above (2) using the method described in WO2005/104835 and the method of Kuroiwa et al. (Kuroiwa et al., Nature Biotechnology, 20, 889-894) is introduced into a somatic cell derived from a host animal by a microcell fusion method. Thereafter, the animal having the human artificial chromosome vector may be constructed by transplanting a nucleus or chromatin agglomerate of the cell into an oocyte and transplanting the oocyte or an embryo to be formed from the oocyte into the uterus of a host animal to give birth.

It may be confirmed by a method of Kuroiwa et al. (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000 and Kuroiwa et al., Nature Biotechnology, 20, 889-894) whether an animal constructed by the above method has the human artificial chromosome vector of the present invention.

4. Method for Producing a Human Antibody of the Present Invention

A antigen-specific human antibody may be produced by immunizing the animal having the human artificial chromosome vector of the present invention constructed in the above (3) with a desired antigen to produce the antigen-specific human antibody in the serum of the animal and recovering the antigen-specific human antibody from the serum.

The antigens for immunizing the animal having the human artificial chromosome vector of the present invention, are not particularly limited and examples include a tumor-associated antigen, an antigen associated with allergy or inflammation, an antigen associated with cardiovascular disease, an antigen associated with autoimmune disease, an antigen associated with neurodegenerative disease, and an antigen associated with viral or bacterial infections.

Examples of tumor-associated antigens include CD1a, CD2, CD3, CD4, CD5, CD6, CD7, CD9, CD10, CD13, CD19, CD20, CD21, CD22, CD25, CD28, CD30, CD32, CD33, CD38, CD40, CD40 ligand (CD40L), CD44, CD45, CD46, CD47, CD52, CD54, CD55, CD55, CD59, CD63, CD64, CD66b, CD69, CD70, CD74, CD80, CD89, CD95, CD98, CD105, CD134, CD137, CD138, CD147, CD158, CD160, CD162, CD164, CD200, CD227, adrenomedullin, angiopoietin related protein 4 (ARP4), aurora, B7-H1, B7-DC, integlin, bone marrow stromal antigen 2 (BST2), CA125, CA19.9, carbonic anhydrase 9 (CA9), cadherin, cc-chemokine receptor (CCR) 4, CCR7, carcinoembryonic antigen (CEA), cysteine-rich fibroblast growth factor receptor-1 (CFR-1), c-Met, c-Myc, collagen, CTA, connective tissue growth factor (CTGF), CTLA-4, cytokeratin-18, DF3, E-catherin, epidermal growth facter receptor (EGFR), EGFRvIII, EGFR2 (HER2), EGFR3 (HER3), EGFR4 (HER4), endoglin, epithelial cell adhesion molecule (EpCAM), endothelial protein C receptor (EPCR), ephrin, ephrin receptor (Eph), EphA2, endotheliase-2 (ET2), FAM3D, fibroblast activating protein (FAP), Fc receptor homolog 1 (FcRH1), ferritin, fibroblast growth factor-8 (FGF-8), FGF8 receptor, basic FGF (bFGF), bFGF receptor, FGF receptor (FGFR)3, FGFR4, FLT1, FLT3, folate receptor, Frizzled homologue 10 (FZD10), frizzled receptor 4 (FZD-4), G250, G-CSF receptor, ganglioside (GD2, GD3, GM2, GM3, and the like), globo H, gp75, gp88, GPR-9-6, heparanase I, hepatocyte growth factor (HGF), HGF receptor, HLA antigen (HLA-DR, and the like), HM1.24, human milk fat globule (HMFG), hRS7, heat shock protein 90 (hsp90), idiotype epitope, insulin-like growth factor (IGF), IGF receptor (IGFR), interleukin (IL-6, IL-15, and the like), interleukin receptor (IL-6R, IL-15R, and the like), integrin, immune receptor translocation associated-4 (IRTA-4), kallikrein 1, KDR, KIR2DL1, KIR2DL2/3, KS1/4, lamp-1, lamp-2, laminin-5, Lewis y, sialyl Lewis x, lymphotoxin-beta receptor (LTBR), LUNX, melanoma-associated chondroitin sulfate proteoglycan (MCSP), mesothelin, MICA, Mullerian inhibiting substance type II receptor (MISIIR), mucin, neural cell adhesion molecule (NCAM), Necl-5, Notch1, osteopontin, platelet-derived growth factor (PDGF), PDGF receptor, platelet factor-4 (PF-4), phosphatidylserine, Prostate Specific Antigen (PSA), prostate stem cell antigen (PSCA), prostate specific membrane antigen (PSMA), Parathyroid hormone related protein/peptide (PTHrP), receptor activator of NF-kappaB ligand (RANKL), receptor for hyaluronic acid mediated motility (RHAMM), ROBO1, SART3, semaphorin 4B (SEMA4B), secretory leukocyte protease inhibitor (SLPI), SM5-1, sphingosine-1-phosphate, tumor-associated glycoprotein-72 (TAG-72), transferrin receptor (TfR), TGF-beta, Thy-1, Tie-1, Tie2 receptor, T cell immunoglobulin domain and mucin domain 1 (TIM-1), human tissue factor (hTF), Tn antigen, tumor necrosis factor (TNF), Thomsen-Friedenreich antigen (TF antigen), TNF receptor, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), TRAIL receptor (DR4, DRS, and the like), system ASC amino acid transporter 2 (ASCT2), trkC, TROP-2, TWEAK receptor Fn14, type IV collagenase, urokinase receptor, vascular endothelial growth factor (VEGF), VEGF receptor (VEGFR1, VEGFR2, VEGFR3, and the like), vimentin, VLA-4, and the like.

Examples of antigens associated with allergy or flare include IL-6, IL-6R, IL-5, IL-5R, IL-4, IL-4R, TNF, TNF receptor, CCR4, chemokine, chemokine receptor, and the like.

Examples of antigens associated with cardiovascular disease include GPIIb/IIIa, PDGF, PDGF receptor, blood coagulation factor, IgE, α_vβ₃, α₃β₇, and the like.

Examples of antigens associated with viral or bacterial infections include gp120, CD4, CCR5, a verotoxin, an anthrax protective antigen, a methicillin-resistant Staphylococcus aureus (MRSA) antigen, a hepatitis type B virus (HBV) antigen, a cytomegalovirus (CMV) antigen, a Rabies antigen, a Varicella zoster antigen, and the like.

Other examples thereof include a T cell surface membrane protein mixtures, a Rh (D) antigen, crotalid venom, digoxin, and the like.

The immunization is carried out by administering the antigen with, for example, a complete Freund's adjuvant or an appropriate adjuvant such as an aluminum hydroxide gel, and pertussis bacteria vaccine, subcutaneously, intravenously, or intraperitoneally into an animal.

Examples of the form of administering the antigen into an animal having the human artificial chromosome vector of the present invention include peptides, protein, bacteria, viruses, cells, biological tissue pieces, and the like.

When the antigen is a partial peptide, a conjugate is produced with a carrier protein such as bovine serum albumin (BSA), keyhole Limpet hemocyanin (KLH) or the like, and is used as the immunogen.

The antigen is administered once to 10 times every 1 to 4 weeks after the first administration. After 1 to 14 days from each administration, blood is collected from the animal to measure the antibody value of the serum.

Examples of the method for detecting and measuring the antigen-specific human antibody included in the serum include a binding assay by an enzyme-linked immunosorbent assay [Antibodies—A Laboratory Manual, Cold Spring Harbor Laboratory (1988)], a biosensor Biacore, and the like.

Specifically, the binding amount of a human antibody in the serum may be measured by incubating the serum comprising the human antibody with antigen expressing cells, and then using an antibody specifically recognizing a human antibody.

Further, in addition to these methods, the antibody may be selected by identifying a target antigen of the antibody according to a method known in the art (The Prostate, 67, 1163, 2007).

Examples of the method for recovering human antibodies from the serum include a method of purifying by adsorbing the human antibody on a protein A carrier, a protein G carrier, or a carrier on which the human immunoglobulin specific antibody is supported.

Further, methods used in purification of proteins, such as gel filtration, ion exchange chromatography, and ultrafiltration, may be combined.

A human antibody produced by the above method may be a polyclonal antibody or a monoclonal antibody, and preferably a polyclonal antibody.

EXAMPLE

Example 1

Construction of a Targeting Vector

(1) Construction of a Targeting Vector pTEL'hisDpuro^lox2272F9R9

Methods described in the publication (Kuroiwa et al., Nat Biotechnol. 18: 1086-1090, 2000, Kuroiwa et al., Nat Biotechnol. 20: 889-894, 2002 and Kuroiwa et al., Nat Biotechnol. 27: 173-181, 2009) were basically used for construction of a targeting vector.

Specifically, a genomic DNA fragment Dk-F9R9 used as a homology arm was amplified by PCR consisting of 40 cycles of 98° C. for 10 seconds and 68° C. for 9 minutes by using two primer DNAs of kD-F9 (5′-tcgaggatccgccagggagacagatgccaagtacggtttag-3′) (SEQ ID NO:1) and kD-R9 (5′-tcgaggatccaggatctttgggggactgaatggggtgtgct-3′) (SEQ ID NO:2) and a genomic DNA of a chicken DT40 cell line KTL1 (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009) having the human chromosome 2 as a template.

Subsequently, the plasmid pTEL'hisDpuro^lox2272 was constructed in the following order.

First, the plasmid pPUR^lox2272 was constructed by annealing two oligo DNA fragments [a DNA fragment consisting of a nucleotide sequence of 5′-agcttggatccataacttcgtataggatactttatacgaagttata-3′ (SEQ ID NO:3) and a DNA fragment consisting of a nucleotide sequence of 5′-agcttataacttcgtataaagtatcctatacgaagttatggatcca-3′ (SEQ ID NO:4)] comprising a modified type lox2272 sequence, followed by cloning into the HindIII site of the plasmid pPUR (BD Bioscience Clontech).

Meanwhile, the plasmid pTEL'hisDPm was constructed by substituting the puromycin resistance gene (hereinafter referred to as puro') of the plasmid pTELpuro (Kuroiwa et al., Nat Biotechnol. 18: 1086-1090, 2000, Kuroiwa et al., Nat Biotechnol. 20: 889-894, 2002, and Kuroiwa et al., Nat Biotechnol. 27: 173-181, 2009) with the hisD gene, substituting the EcoRI site with the SrfI site, and substituting the SpeI site with the PmeI site.

After generating the BamHI-digested fragment of the pPUR^lox2272 blunt ended, the obtained fragment was cloned into the PmeI site of the pTEL'hisDPm and thus obtained plasmid was named as the pTEL'hisDpuro^lox2272.

The plasmid pTEL'hisDpuro^lox2272F9R9 was constructed by subcloning the Dk-F9R9 amplified by the above PCR into the BamHI site of the pTEL'hisDpuro^lox2272 (FIG. 4).

(2) Construction of a Targeting Vector pTELCAGzeoSLF2R2

In the same manner as in (1), the pTELCAGzeo(Sr)Pm was constructed by substituting the EcoRI site of the plasmid pTELpuro with the SrfI site, then substituting the SrfI site with the PmeI site, and further substituting the puro gene with the CAGzeo gene.

Meanwhile, a genomic DNA fragment used as a homology arm was amplified by repeating 40 cycles of 98° C. for 10 seconds and 68° C. for 9 minutes by using SL-F2 (5′-tcgaggatccggcctcccaaaggattatagacgtgagccactgt-3′) (SEQ ID NO:5) and SL-R2 (5′-tcgaggatccaaagaaggggcccgcctctgcctctaaatcctgac-3′) (SEQ ID NO:6) as a PCR primer set and a chromosome DNA of a chicken DT40 cell line 52-18 (Kuroiwa et al., Nucleic Acids Res 26: 3447-3448, 1998) having the human chromosome 22 as a template.

The pTELCAGzeoSLF2R2 was constructed by subcloning the PCR product obtained into the BamHI site of the plasmid pTELCAGzeo(Sr)Pm (FIG. 5).

(3) Construction of a Targeting Vector p553CAG^lox2272BsrDT

A vector having a structure in which a targeting vector pHCF2loxPHyg (Kuroiwa et al., Nat Biotechnol. 18: 1086-1090, 2000) was substituted with the AP000553 site (GenBank accession Number) sequence in which a homology arm sequence of the HCF2 gene was amplified by PCR was constructed and used as the targeting vector p553loxPHyg(F).

At that time, the amplification of the AP000553 site fragment was carried out by PCR consisting of 40 cycles of 98° C. for 10 seconds and 68° C. for 15 minutes by using 553-F3 (5′-tgtagctgactttagccacccacaagtac-3′) (SEQ ID NO:7) and 553-R3 (5′-cttgctgattatacctcatctccttccctc-3′) (SEQ ID NO:8) as a primer set and a genomic DNA of the chicken DT40 cell 52-18 as a template.

After the obtained plasmid p553loxPHyg(F) was digested with NotI, a self-ligation was carried out, followed by cloning of the diphtheria toxin A fragment (hereinafter referred to as DT-A) into the Srf site.

Meanwhile, the pDRIVE-CAG (InvivoGen) was modified as follows. The oligo DNAs [5′-gtacaataacttcgtatagcatacattatacgaagttatagatctg-3′ (SEQ ID NO:9) and 5′-aattcagatctataacttcgtataatgtatgctatacgaagttatt-3′ (SEQ ID NO:10)] each comprising the loxP sequence were annealed and the lacZ fragment of the pDRIVE-CAG was substituted. The pCAG^loxP was constructed by cloning the fragment digested with SdaI and SwaI into the pBluescript SK-(Stratagene) digested with PstI and SmaI.

Subsequently, the loxP sequence of the pCAG^loxP was substituted with a sequence comprising the lox2272 produced by annealing the two oligo DNAs [5′-gatctataacttcgtataggatactttatacgaagttatg-3′ (SEQ ID NO:11) and 5′-ctagcataacttcgtataaagtatcctatacgaagttata-3′ (SEQ ID NO:12)]. Further, the pCAG^loxP2272bsr was constructed by inserting the blasticidin-resistance gene (bsr gene) into the SpeI site.

Finally, the p553CAG^lox2272BsrDT (FIG. 6) was completed by cloning the NotI-KpnI fragment (CAG-lox2272-polyA-bsr) into the NotI site.

(4) Construction of a Targeting Vector pSC355CAG^lox511hisDDT

A genomic DNA used as a homology arm was amplified by PCR consisting of 40 cycles of 98° C. for 10 seconds and 68° C. for 15 minutes by using SC355-F3 (5′-gtacaatcttggatcactacaacctctgcctacca-3′) (SEQ ID NO:13) and SC355-R3 (5′-tgctgtgtctaatcaggtgttgaacccatctacta-3′) (SEQ ID NO:14) as a primer set and a genomic DNA of the chicken DT40 cell comprising the human chromosome 14 as a template.

The KpnI site of the plasmid pBluescript was substituted with the SrfI site, and the DNA fragment amplified above was subcloned into the SpeI site. The obtained plasmid was used as the pSC355F3R3.

Subsequently, the loxP sequence of the pCAG^loxP was substituted with a sequence comprising lox511 produced by annealing the two oligo DNAs [a DNA fragment consisting of the sequence 5′-gatctataacttcgtatagtatacattatacgaagttatg-3′ (SEQ ID NO:15) and a DNA fragment consisting of the nucleotide sequence 5′-ctagcataacttcgtataatgtatactatacgaagttata-3′ (SEQ ID NO:16)] and used as the pCAG^lox511.

The pCAG^lox511hisD was constructed by inserting the hisD gene into the SpeI site of the pCAG^lox511. A fragment (CAG-lox511-polyA-hisD) digested with NotI and KpnI was cloned into the EcoRV site of the pSC355F3R3. Finally, the plasmid obtained by subcloning the DT-A fragment into the Notl site was used as the pSC355CAG^lox511hisDDT (FIG. 7).

(5) Construction of a Targeting Vector p14CEN(FR)hygpuro^lox511DT

A genomic DNA used as a homology arm was amplified by PCR consisting of 40 cycles of 98° C. for 10 seconds and 68° C. for 15 minutes by using 14 CEN-F (5′-tcgaggatccttcgccaccccaaagatgattacagattac-3′) (SEQ ID NO:17) and 14 CEN-R (5′-tcgaggatcctacactagaagcacaaaccccaccattacacat-3′) (SEQ ID NO:18) as a primer set and a genomic DNA of the chicken DT40 cell comprising the human chromosome 14 as a template.

The p14CEN(FR) was constructed by subcloning the PCR product into the BamHI site of the pBluescript in which the KpnI site was substituted with the PmeI site.

The oligo DNAs [a DNA fragment consisting of a nucleotide sequence of 5′-agcttggatccataacttcgtatagtatacattatacgaagttata-3′ (SEQ ID NO:19) and a DNA fragment consisting of a nucleotide sequence of 5′-agcttataacttcgtataatgtatactatacgaagttatggatcca-3′ (SEQ ID NO:20)] comprising the lox511 sequence were annealed. The plasmid pPUR^lox511 was constructed by cloning the fragment obtained into the HindIII site of the plasmid pPUR (BD Bioscience Clontech).

The pHygPuro^lox511 was constructed by cloning the BamHI-digested fragment of the pPUR^lox511 into the BamHI site of the pBluescript, and the hygromycin resistance gene (hyg gene) into the EcoRV site, respectively.

A fragment (puro-lox511-hyg) digested with Notl and Kpnl was cloned into the HpaI site of the p14CEN(FR). Finally, the p14CEN(FR)hygpuro^lox511DT (FIG. 8) was completed by subcloning the DT-A fragment into the PmeI site.

(6) Construction of a Targeting Vector pRNR2^loxPbsrDT

The targeting vector pRNR2^loxPbsrDT (FIG. 9) was constructed by inserting the DT-A fragment into the vector pRNR2^loxP (Kuroiwa et al., Nat Biotechnol. 18: 1086-1090, 2000).

(7) Construction of a Targeting Vector pCH2CAGzeoDT

A λ phage genomic library of κHAC (WO2009/111086) was constructed from the CHO cell comprising κHAC by a Custom Library Construction Service (Loftstrand Labs, Ltd.) by using the λFIX II vector.

A clone comprising the human IgM constant region from the constructed genomic library was screened by using, as a probe, a PCR product amplified by PCR consisting of 40 cycles of 98° C. for 10 seconds, 64° C. for 30 seconds, and 72° C. for 1 minute with DNAs consisting of nucleotide sequences of 5′-cagtccccggcagattcaggtgtcc-3′ (SEQ ID NO:89) and of 5′-gaaagtggcattggggtggctctcg-3′ (SEQ ID NO:90) as a primer and a chromosome DNA extracted from the CHO cell (WO2009/111086) comprising KHAC as a template. As a result, clones #1, #4, and #7 were isolated.

Meanwhile, the SeSp fragment produced by annealing the oligo DNAs consisting of nucleotide sequences of 5′-ggaccaggtggagactgtgcagtcctcacccataactttcagggcctacagcatgctg-3′ (SEQ ID NO:21) and 5′-cagcatgctgtaggccctgaaagttatgggtgaggactgcacagtctccacctggtcc-3′ (SEQ ID NO:22) was cloned into the blunt-ended PstI site of pBluescript.

The pmAYSpB was constructed by subcloning a fragment (about 2 kb) digested with SphI and BamHI from the plasmid pBCμAY37-95 in which the SalI-bovine IGHM chromosome fragment was cloned into the pBluescript, into the SphI-BamHI site of the plasmid obtained above.

Similarly, the pmAYSpBPml was constructed by subcloning a fragment (about 2 kb) digested with BamHI and PmlI of the pBCμAY37-95 into the BamHI-PmlI site (with which the original SpeI site is substituted) of the pmAYSpB.

The pRISe was constructed by subcloning the EcoRI-SexAI fragment (about 0.6 kb) of the above clone #1 into the EcoRI-SexA1 site of the pmAYSpBPm1.

Subsequently, the pRISeCAGzeo(R) was constructed by subcloning the CAGzeo into which the loxP sequence was introduced, into the Van91I site of the pRISe. Further, the pRISeCAGzeoE was constructed by substituting the NotI site of the pRISeCAGzeo(R) with the EcoRI site.

Meanwhile, the pCH2S(F) was constructed by subcloning the PmlI fragment (about 1.7 kb) of the above clone #4 into the SmaI site of the pBluescript in which the EcoRV site was substituted with the MluI site.

The pCH2LS was constructed by cloning a fragment (about 6.6 kb) digested with MluI and EcoRI of the above clone #1 into the MluI-EcoRI site of the pCH2S(F).

Subsequently, the pCH2CAGzeo(F) was constructed by subcloning the EcoRI fragment of the pRISeCAGzeoE into the EcoRI site of the pCH2LS. Finally, the pCH2CAGzeoDT (FIG. 10) was completed by subcloning the DT-A fragment into the NotI site of the pCH2CAGzeo(F).

Example 2

Construction of KSL-HAC

(1) Modification of the Human Chromosome 2 in a Chicken DT40 Cell

In order to generate a deletion at the AP104134 site of the human chromosome 2 and insert a lox2272 sequence and a promoterless puro^r cassette, the targeting vector pTEL'hisDpurolox2272F9R9 was linearized with SrfI (Stratagene) and introduced into KTL1 (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009) which was a chicken DT40 cell line having the human chromosome 2 fragment digested at the CD8A gene locus by electroporation (550 V, 25 μF). The electroporation of the DT40 cell was carried out by a method described in the publication (Kuroiwa et al., Nat. Biotechnol. 18: 1086-1090, 2000).

Colonies were subjected to selection by histidinol (0.5 mg/ml, Sigma) for two weeks and the sensitivity to puromycin (1 μg/ml, Sigma) was measured as an index of deletion of the puro^r cassette on the CD8A gene locus.

The chromosome DNA was extracted from a colony having the puromycin sensitivity by using the Gentra Puregene cell kit (QIAGEN), and was subjected to a PCR screening using the FABP1-F (5′-tatcaagggggtgtcggaaatcgtg-3′) (SEQ ID NO:23) and the FABP1-R (5′-actgggcctgggagaacctgagact-3′) (SEQ ID NO:24) as primers.

PCR was carried out under a condition of amplifying the FABP1 gene locus which was present in KTL1 but was not present at a target clone and a condition of repeating 30 cycles of 98° C. for 10 seconds, 60° C. for 30 seconds, and 72° C. for 1 minute. As a result, clone K53 was identified as a clone in which a deletion exactly occurred. FIG. 11 illustrates an outline of a method for modifying the human chromosome 2 in a chicken DT40 cell.

(2) Modification of the Human Chromosome 22 in a Chicken DT40 Cell

In order to generate a deletion at the AP000350 site which is positioned on about 450 Mb telomere side from the AP000344 site (Kuroiwa et al., Nat. Biotechnol. 20: 889-894, 2002) of the human chromosome 22, the targeting vector pTELCAGzeoSLFR was linearized with PmeI (New England Biolabs) and introduced into 52-18 (Kuroiwa et al., Nucleic Acids Res 26: 3447-3448, 1998) which is a chicken DT40 cell line having the human chromosome 22 by electroporation (550 V, 25 μF).

A colony was subjected to selection by Zeocin (1 mg/ml, Invitrogen) for 2 weeks. A genomic DNA extracted from the thus obtained colony was subjected to PCR screening by using 350T-F (5′-gaggtgggctgaggggcaagtgtg-3′) (SEQ ID NO:25) and 350T-R (5′-tacgaggaggggaggcagtgagagg-3′) (SEQ ID NO:26) as primers.

PCR was carried out under conditions (repeating 30 cycles of 98° C. for 10 seconds, 63° C. for 30 seconds, and 72° C. for 1 minute) in which the AP000350 site which was present at 52-18 but was not present at a clone in which the targeting occurred, was amplified. As a result, clone ST13 was identified as a clone in which a deletion was generated exactly.

In order to integrate a lox2272 sequence and a CAG promoter into the AP000553 site, the targeting vector p553CAGlox2272bsrDT which was linearized with PmeI (New England Biolabs) was introduced into ST13 by electroporation (550 V, 25 μF).

A colony was subjected to selection by blasticidin S (15 μg/ml, Invitrogen) for 2 weeks. A genomic DNA was extracted from the thus obtained colony and was subjected to PCR screening by using 553KO-F (5′-gtcagccaggcgggccatttaccgtaagttatgta-3′) (SEQ ID NO:27) and 553KO-R (5′-agggctgggttagatggcaccaaatgaaaggagaa-3′) (SEQ ID NO:28) as primers. PCR was carried out by repeating 40 cycles of 98° C. for 10 seconds and 68° C. at 6 minutes. As a result, clone STL54 was identified as a clone in which a targeting occurred. FIG. 12 illustrates an outline of a method for modifying the human chromosome 22 in a chicken DT40 cell.

(3) Construction of a SLKH Fragment in a DT40 Hybrid Cell

A SLKH fragment was constructed in a chicken DT40 hybrid cell according to a method of the publication (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009).

The K53 (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009) comprising a fragment derived from the human chromosome 2 having a hyg^r cassette prepared in Example 2(1) and the STL54 comprising a fragment derived from the human chromosome 22 having a bs^r cassette prepared in Example 2(2) were fused by using the PEG1500 (Roche) to prepare a DT40 hybrid cell.

The colony was maintained in the presence of hygromycin B (1.5 mg/ml, Invitrogen) and blasticidin S (20 μg/ml, Invitrogen) for 3 weeks to select a cell maintaining both human chromosome fragments. A genomic DNA was extracted from the colony and was subjected to PCR.

It was confirmed whether the human chromosome 2 fragment was maintained by carrying out PCR which repeated 40 cycles consisting of 98° C. for 10 seconds and 65° C. for 8 minutes when cos138KO-F and cos138KO-R were used and 40 cycles consisting of 98° C. for 10 seconds, 60° C. for 30 seconds, and 72° C. for 1 minute for other cases, respectively, using primer combinations of PCR1 to PCR5 shown in Table 1.

TABLE 1
Combinations of Primers for PCR
	Primer	Nucleotide sequence of primer
PCR 1	IGKC-F	5′-tggaaggtggataacgccct-3′
		(SEQ ID NO: 29)
	IGKC-R	5′-tcattctcctccaacattagca-3′
		(SEQ ID NO: 30)
PCR 2	IGKV-F	5′-agtcagggcattagcagtgc-3′
		(SEQ ID NO: 31)
	IGKV-R	5′-gctgctgatggtgagagtga-3′
		(SEQ ID NO: 32)
PCR 3	RPIA-F	5′-cttacccaggctccaggctctatt-3′
		(SEQ ID NO: 33)
	RPIA-R	5′-ctctacctccctaccccatcatcac-3′
		(SEQ ID NO: 34)
PCR 4	EIF2AK3-F	5′-aggtgctgctgggtggtcaagt-3′
		(SEQ ID NO: 35)
	EIF2AK3-R	5′-gctcctgcaaatgtctcctgtca-3′
		(SEQ ID NO: 36)
PCR 5	cos138KO-F	5′-tctttctctcacctaattgtcctggc-3′
		(SEQ ID NO: 37)
	cos138KO-R	5′-aggactggcactcttgtcgatacc-3′
		(SEQ ID NO: 38)

It was confirmed whether the human chromosome 22 fragment was maintained by carrying out PCR1 to 8 by the following reaction cycle, for each case with a combination of PCR1 to PCR8 primers shown in the following Table 2.

For each PCR reaction, PCR1 and 7 were carried out at 40 cycles of 98° C. for 10 seconds, 60° C. for 30 seconds, and 72° C. for 1 minute, PCR2 and 3 were carried out at 40 cycles of 98° C. for 10 seconds, 63° C. for 30 seconds, and 72° C. for 1 minute, PCR4 and 5 were carried out at 40 cycles of 98° C. for 10 seconds, 56° C. for 30 seconds, and 72° C. for 1 minute, PCR6 was carried out at 40 cycles of 98° C. for 10 minutes, 65° C. for 30 seconds, and 72° C. for 1 minute, and PCR8 was carried out at 40 cycles of 98° C. for 10 seconds and 68° C. for 6 minutes.

TABLE 2
Combinations of Primers for PCR
	Primer name	Nucleotide sequence of primer
PCR 1	553P-F	5′-agatctcttgagcccagcagtttga-3′
		(SEQ ID NO: 39)
	553P-R	5′-tgaagttagccggggatacagacg-3′
		(SEQ ID NO: 40)
PCR 2	hVpreB1-F	5′-tgtcctgggctcctgtcctgctcat-3′
		(SEQ ID NO: 41)
	hVpreB1-R	5′-ggcggcggctccaccctctt-3′
		(SEQ ID NO: 42)
PCR 3	hVpreB3-F	5′-cactgcctgcccgctgctggta-3′
		(SEQ ID NO: 43)
	hVpreB3-R	5′-gggcggggaagtgggggagag-3′
		(SEQ ID NO: 44)
PCR 4	IgL-F	5′-ggagaccaccaaaccctccaaa-3′
		(SEQ ID NO: 45)
	IgL-R	5′-gagagttgcagaaggggtgact-3′
		(SEQ ID NO: 46)
PCR 5	344-F	5′-atcatctgctcgctctctcc-3′
		(SEQ ID NO: 47)
	344-R	5′-cacatctgtagtggctgtgg-3′
		(SEQ ID NO: 48)
PCR 6	hL5-F	5′-agccccaagaacccagccgatgtga-3′
		(SEQ ID NO: 49)
	hL5-R	5′-ggcagagggagtgtggggtgttgtg-3′
		(SEQ ID NO: 50)
PCR 7	350P-F	5′-accagcgcgtcatcatcaag-3′
		(SEQ ID NO: 51)
	350P-R	5′-atcgccagcctcaccatttc-3′
		(SEQ ID NO: 52)
PCR 8	553KO-F	5′-gtcagccaggcgggccatttaccgtaag
		ttatgta-3′
		(SEQ ID NO: 53)
	553KO-R	5′-agggctgggttagatggcaccaaatgaa
		aggagaa-3′
		(SEQ ID NO: 54)

Further, a fluorescence in situ hybridization (FISH) using the HUMAN Cot-1 DNA (Invitrogen) as a probe was carried out according to a method in the publication (Kuroiwa et al., Nat. Biotechnol. 18: 1086-1090, 2000), and it was confirmed that two human chromosome fragments had appropriate sizes (the human chromosome 2 fragment was about 154 Mb and the human chromosome 22 fragment was about 24 Mb of). As a result, clone SLK2 was identified as a positive clone.

In order to generate a site specific recombination between two lox2272 sites each arranged at the AC104134 site on the human chromosome 2 fragment and at the AP000553 site on the human chromosome 22 fragment, the Cre expression plasmid was introduced into SLK2 by electroporation (550 V, 25 μF).

A recombinant was selected in the presence of puromycin (1 to 5 μg/ml, Invitrogen) for 10 days by using the puromycin resistance imparted by the CAG promoter-lox2272-puro^r cassette generated at the translocation position.

Further, the recombination was confirmed by PCR (40 cycles of 98° C. for 10 seconds and 68° C. for 1.5 minutes) using CAGpuro-F3 (5′-gcggcgccggcaggaaggaaatg-3′) (SEQ ID NO:55) and CAGpuro-R3 (5′-cgaggcgcaccgtgggcttgta-3′) (SEQ ID NO:56) as primers and sequencing analysis of PCR products.

As a result, SLKH6 was identified as a clone in which a desired translocation was occurred to maintain the SLKH fragment. FIG. 13 illustrates an outline of a method for constructing the SLKH fragment in a DT40 hybrid cell.

(4) Transfer of a SLKH Fragment into a DT40 Cell Wild Type by MMCT (Microcell-Mediated Chromosome Transfer) Method

The SLKH fragment in Example 2(3) was transferred from a DT40 hybrid cell line SLKH6 into a wild type DT40 cell by the MMCT method (Kuroiwa et al., Nat. Biotechnol. 18: 1086-1090, 2000). The puromycin resistant cell was selected in the presence of puromycin (0.5 μg/ml, Invitrogen) for 2 weeks by fusing micronuclei purified from SLKH6 with 2×10⁷ of DT40 cells by using PEG1500 (Roche).

When a colony in which the SLKH fragment was transferred into DT40 was isolated, the colony had lost resistance to blasticidin and therefore the test for sensitivity of the colony to blasticidin S (10 μg/ml, Invitrogen) was carried out. Further, it was confirmed that the SLKH fragment was maintained by extracting a genomic DNA from the colony with sensitivity to blasticidin S and using the following combination of PCR primers.

That is, a combination of IGKC-F and IGKC-R, a combination of IGKV-F and IGKV-R, a combination of RPIA-F and RPIA-R, a combination of EIF2AK3-F and EIF2AK3-R, a combination of cos138KO-F and cos138KO-R, a combination of CAGpuro-F3 and CAGpuro-R3, a combination of 553P-F and 553P-R, a combination of hVpreB1-F and hVpreB1-R, a combination of hVpreB3-F and hVpreB3-R, a combination of IgL-F and IgL-R, a combination of 344-F and 344-R, a combination of hL5-F and hL5-R, a combination of 350P-F and 350P-R, and a combination of 553KO-F and 553 KO-R were used [all described in Example 2(3)].

In addition, it was confirmed that only one human chromosome fragment (a fragment with about 154 Mb, which is equivalent to the SLKH fragment) was present by FISH using the HUMAN Cot-1 DNA (Invitrogen) as a probe. The presence of the SLKH fragment was confirmed by carrying out two-color FISH method according to an attached protocol by using a chromosome 2 painting probe labeled with rhodamine, a chromosome 22 painting probe labeled with fluoresceine (all from MP Biomedicals), and DAPI (Abbott Molecular) as a counter staining. As a result, clones SLKD17 and SLKD18 were identified as positive clones.

(5) Construction of KSL-HAC in a DT40 Hybrid Cell

KSL-HAC was constructed in the following DT40 hybrid cell according to a method described in the publication (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009).

First, a DT40 hybrid cell was constructed by fusing SLKD18 having the hyg^r cassette obtained in Example 2(4) with a DT40 cell line R56 (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009) comprising the SC20 fragment having the bs^r cassette by using PEG1500 (Roche).

The colony was maintained in the presence of hygromycin B (1.5 mg/ml, Invitrogen) and blasticidin S (20 μg/ml, Invitrogen) for 3 weeks to select a cell maintaining both of the SLKH fragment and the SC20. A genomic DNA was extracted from the colony and was subjected to PCR.

PCR for confirming whether the SLKH fragment was maintained was carried out by using primer combinations of IGKC-F and IGKC-R, IGKV-F and IGKV-R, RPIA-F and RPIA-R, EIF2AK3-F and EIF2AK3-R, cos138KO-F and cos138KO-R, CAGpuro-F3 and CAGpuro-R3, 553P-F and 553P-R, hVpreB1-F and hVpreBl-R, hVpreB3-F and hVpreB3-R, IgL-F and IgL-R, 344-F and 344-R, hL5-F and hL5-R, 350P-F and 350P-R, and 553KO-F and 553 KO-R [all described in Example 2(3)].

PCR for confirming whether the SC20 fragment was maintained was carried out with primers and reaction conditions, described in the following Table 3.

Further, two human chromosome fragments having an appropriate size (the SLKH fragment was about 156 Mb and SC20 was about 26 Mb) were confirmed by FISH using the HUMAN Cot-1 DNA (Invitrogen) as a probe. As a result, clone KSL3 was identified as a positive clone.

TABLE 3
Combination of Primers for PCR and reaction cycles
PCR 1	RNR2-1	5′-tggatgtatcctgtcaagagacc-3′	40 cycles of 98° C. for 10 seconds
		(SEQ ID NO: 57)	and 65 C. for 5 minutes
	STOP-3	5′-cagacactctatgcctgtgtgg-3′
		(SEQ ID NO: 58)
PCR 2	VH3-F	5′-agtgagataagcagtggatg-3′	40 cycles of 98° C. for 10 seconds,
		(SEQ ID NO: 59)	56° C. for 30 seconds and 72° C. for
	VH3-R	5′-cttgtgctactcccatcact-3′	1 minute
		(SEQ ID NO: 60)
PCR 3	g1(g2)-F	5′-accccaaaggccaaactctccactc-3′	40 cycles of 98° C. for 10 seconds,
		(SEQ ID NO: 61)	60° C. for 30 seconds and 72° C. for
	g1(g2)-R	5′-cacttgtactccttgccattcagc-3′	1 minute
		(SEQ ID NO: 62)
PCR 4	SC355-F2	5′-tcgagtcgacatggccccaggaggagctgagtggcacgagtgtaa-3′	40 cycles of 98° C. for 10 seconds
		(SEQ ID NO: 63)	and 68° C. for 11 minutes
	SC355-R2	5′-tcgagtcgacggaagatggcccacgtgattgctgcctgcctctac-3′
		(SEQ ID NO: 64)
PCR 5	SC858-F4	5′-tcgagtcgaccacgctgccaaacccccggaaacacgaaatc-3′	40 cycles of 98° C. for 10 seconds
		(SEQ ID NO: 65)	and 68° C. for 11 minutes
	SC858-R4	5′-tcgagtcgaccaccccacatccacccccactgccccttacc-3′
		(SEQ ID NO: 66)
PCR 6	CH3-F3	5′-aggccagcatctgcgaggat-3′	40 cycles of 98° C. for 10 seconds,
		(SEQ ID NO: 67)	60° C. for 30 seconds and 72° C. for
	CH4-R2	5′-gtggcagcaagtagacatcg-3′	1 minute
		(SEQ ID NO: 68)

In order to cause a site specific recombination between two loxP sites each arranged on the cos138 site (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009) of the SLKH fragment (a region derived from chromosome 2) and the RNR2 gene locus of the SC20 fragment, a Cre expression plasmid was introduced into KSL3 by electroporation (550 V, 25 μF).

Since the GFP expression capability is imparted by the PGK promoter-loxP-GFP cassette formed at the translocation site, GFP positive cells were sorted by using FACSAria according to a method described in the publication (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009), and a recombinant was concentrated. In order to obtain a GFP positive cell with a purity of 95% or more, the sorting was carried out twice.

The GFP cassette was confirmed by PCR consisting of 40 cycles of 98° C. for 10 seconds, 59° C. for 30 seconds, and 72° C. for 1 minute by using PGK2 (5′-tgttctcctatcctcatctcc-3′) (SEQ ID NO:69) and GFP2 (5′-tgaaggtagtgaccagtgttgg-3′) (SEQ ID NO:70) as primers.

Clone KSLH12(2) was identified as a clone which generates a desired translocation to maintain KSL-HAC. FIG. 14 illustrates an outline of a method for constructing KSL-HAC in a DT40 hybrid cell.

(6) Transfer of KSL-HAC from a DT-40 Hybrid Cell into a CHO Cell by MMCT Method and WCF Method (Whole Cell Fusion)

KSL-HAC in (5) was transferred from the DT40 hybrid cell line KSLH12(2) into Chinese Hamster Ovary (CHO) cells by a partially modified method of a MMCT method or WCF method described in the publication (Kuroiwa et al., Nat. Biotechnol. 18: 1086-1090, 2000).

As for the MMCT method, micronuclei purified from KSLH12(2) were fused with about 2×10⁷ of CHO cells by using PEG1500 (Roche), and selection was carried out in the presence of G418 (600 μg/ml, Invitrogen) and Ouabain (10⁻⁵ mol/L, Sigma) for 3 weeks.

As for the WCF method, 2×10⁷ of KSLH12(2) cells and 2×10⁷ of CHO cells were fused by using PEG1500 (Roche), and selection was carried out in the presence of G418 (600 μg/ml, Invitrogen) and Ouabain (10⁻⁵ mol/L, Sigma) for 3 weeks.

A G418 resistant colony was selected and a genomic DNA was extracted and subjected to PCR screening.

It was confirmed by PCR using the following primer combinations whether KSL-HAC was maintained. That is, a combination of IGKC-F and IGKC-R, a combination of IGKV-F and IGKV-R, a combination of RPIA-F and RPIA-R, a combination of EIF2AK3-F and EIF2AK3-R, a combination of cos138KO-F and cos138KO-R, a combination of CAGpuro-F3 and CAGpuro-R3, a combination of 553P-F and 553P-R, a combination of hVpreB1-F and hVpreB1-R, a combination of hVpreB3-F and hVpreB3-R, a combination of IgL-F and IgL-R, a combination of 344-F and 344-R, a combination of hL5-F and hL5-R, a combination of 350P-F and 350P-R, and a combination of 553KO-F and 553 KO-R [all described in Example 2(3)], and a combination of VH3-F and VH3-R, a combination of g1(g2)-F and g1(g2)-R, a combination of SC355-F2 and SC355-R2, a combination of SC858-F4 and SC858-R4, a combination of CH3-F3 and CH4-R2, and a combination of PGK2 and GFP2 [all described in Example (5)] were used as primer sets of PCR.

Further, it was confirmed by FISH using the Human Cot-1 DNA (invitrogen) as the probe whether KSL-HAC was maintained.

In addition, the presence of the gene loci of the human immunoglobulin heavy chain (IgH), the immunoglobulin κ chain (Igκ), and the immunoglobulin λ chain (Igλ) on KSL-HAC was confirmed by a three-color FISH using the BAC clone RP11-417P24, RP11-316G9, and RP11-22M5 from Roswell Park Cancer Institute Human Male BAC Library (RPCI-11), (Advanced Geno Techs Co.) as probes.

R 11-417P24 was labeled with Red-dUTP, RP11-316G9 with Green-dUTP, and RP11-22M5 with Orange-dUTP, respectively, by using the Nick Translation Kit (Abbott Molecular) to develop chromosomes on the slide, and all the three probes were used for hybridization according to a document attached to the product. Here, DAPI II (Abbott Molecular) was used for counter staining.

Finally, for clone KSLC5 obtained by the MMCT method and clone KSLC20 obtained by the WCF method, a Comparative Genomic Hybridization (CGH) analysis was carried out with Roche NimbleGen by a custom-made array using about 72000 probes covering the gene loci of human IgH, Igκ, and Igλ. As a result, it was shown that both clones had a homologous structure.

Example 3

Construction of KSL-HACΔ

(1) Modification of the Human Chromosome 14 in a DT40 Cell

In order to integrate a lox511 sequence and a CAG promoter on the AL512355 site which is positioned on the centromere side about 300 kb from the IgH gene locus, the targeting vector pSC355CAGlox511hisDDT linearized with SrfI (Stratagene) was introduced into the DT40 cell maintaining an intact human chromosome 14 labeled with pSTneo [Katoh et al., Cell Structure and Function, 12, 575-580, 1987; Japanese Collection of Research Biologicals (JCRB) Bank, Deposit Number VE039] by electroporation (550 V, 25 μF). The electroporation method into the DT40 cell is described in the publication (Kuroiwa et al., Nat. Biotechnol. 18: 1086-1090, 2000).

The colony was subjected to selection by histidinol (0.5 mg/ml, Sigma) for two weeks, and thus a genomic DNA extracted from the resistant colony was subjected to PCR screening.

PCR was carried out with 40 cycles of 98° C. for 10 seconds and 68° C. for 6 minutes by using primers amplifying a clone in which the targeting occurred SC355KO-F2 (5′-acggcgtgaggaccaaggagcgaaacc-3′) (SEQ ID NO:71) and SC355KO-R2 (5′-tgagcgacgaattaaaacaggcgatgac-3′) (SEQ ID NO:72) and also with 40 cycles of 98° C. for 10 seconds, 60° C. for 30 seconds, and 72° C. for 1 minute by using primers amplifying a clone in which vector fragments were randomly integrated 355N-F (5′-gggcaacatagcaagacaccattc-3′) (SEQ ID NO:73) and 355N-R (5′-tcctctcacctcagcctccatagta-3′) (SEQ ID NO: 74).

As a result, clone I355-2 was identified as a clone which generated the targeting.

Subsequently, in order to insert a lox511 sequence and a promoterless puro^r cassette into the AL391156 region on the centromere side 85 Mb from the AL5I2355 site, the targeting vector p14CEN(FR)hygpuro lox511DT linearized with NotI (Roche) was introduced into 1355-2 by electroporation (550 V, 25 μF).

The colony was subjected to selection by hygromycin (1.5 mg/ml, Introgen) for two weeks, and thus a genomic DNA extracted from the resistant colony was subjected to PCR screening. It was determined by PCR under conditions of 40 cycles of 98° C. for 10 seconds and 68° C. for 5 minutes by using the primers 14CENKO-F3 (5′-actgaaatattttaaatgtttgcccttcccactcc-3′) (SEQ ID NO:75) and 14CENKO-R3 (5′-agacctccgcgccccgcaacctccccttctac-3′) (SEQ ID NO:76) whether or not the targeting occurred.

Further, a random insertion was determined by PCR under conditions of 30 cycles of 98° C. for 10 seconds, 60° C. for 30 seconds, and 72° C. for 1 minute by using the primers 14CEN(N)-F2 (5′-aacagttgaatttatggggagtc-3′) (SEQ ID NO:77) and 14CEN(N)-R2 (5′-tcaggattaaacacagtatcacag-3′) (SEQ ID NO:78).

As a result, clone I156-10 was identified as a clone in which the targeting was completed.

In order to achieve a reduction from about 106 Mb to 21 Mb by deleting a sequence of about 85 Mb from the human chromosome 14 by generating a site specific recombination between two lox511 sites each disposed on the AL512355 site and the AL391156 site, a Cre expression plasmid was introduced into the I156-10 by electroporation (550 V, 25 μF).

Since the puromycin resistance was imparted by a CAG promoter-lox511-puro^r cassette formed at a recombination site, the colony was cultured for 4 days and was subjected to selection by puromycin (5 μg/ml, Sigma). The sequences of PCR products were analyzed by carrying out PCR using the primers CAGpuro-F3 and CAGpuro-R3 described in Example 2(3), and thus the presence of the cassette was confirmed.

Further, in order to confirm that both of hisD and hyg^r cassettes was lost as a result of deletion of the 85 Mb, the sensitivity to histidinol (0.5 mg/ml, Sigma) and hygromycin (1.5 mg/ml, Invitrogen) was analyzed. In addition, it was confirmed that the human chromosome 14 was shortened by FISH using the Human Cot-1 DNA (Invitrogen) as a probe.

In the above, clone D8 was identified as a clone in which a desired deletion was achieved.

In order to integrate a loxP sequence into a GFP code sequence on the RNR2 gene locus (Kuroiwa et al., Nat. Biotechnol. 27: 173-181, 2009) of the human chromosome 14, the targeting vector pRNR2loxPbsrDT linearized with SwaI (Roche) was introduced into clone D8 by electroporation (550 V, 25 μF).

The colony was subjected to selection by blasticidin S (20 μg/ml, Invitrogen) for two weeks, and a genomic DNA of the resistant colony was subjected to PCR screening using the primers RNR2-1 and STOP-3 described in Example 2(5).

As a result, clones 14D1 and 14D3 were identified as positive clones maintaining the 14D fragment.

In order to construct a chimeric IgM by substituting the CH2 domain to the TM2 domain of the human immunoglobulin μ heavy chain constant region with bovine-derived sequences, the targeting vector pCH2CAGzeoDT(F) linearized with SalI (Roche) was introduced into clone 14D1 by electroporation (550 V, 25 μF).

The colony was subjected to Zeocin (1 mg/ml, Invitrogen) selection for two weeks, and thus a genomic DNA of the resistant colony was subjected to PCR screening. PCR was carried out under conditions of 40 cycles of 98° C. for 10 seconds and 68° C. for 5 minutes by using the primers cHAC-F (5′-acgcctgctcgcctgcccgctcgcttct-3′) (SEQ ID NO:79) and cHAC-R (5′-ttgccagggccacagttaacggatacg-3′) (SEQ ID NO:80).

The ligated part at 5′ and 3′ of the bovine sequence and the human sequence was confirmed by analyzing the sequences of the PCR products by carrying out PCR under conditions of 40 cycles of 98° C. for 10 seconds, 64° C. for 30 seconds, and 72° C. for 1 minute by using the primers CH2 5′-F (5′-cagcaccccaacggcaacaaagaaa-3′) (SEQ ID NO:81) and CH2 5′-R (5′-ccccagggctgcactcaccaacat-3′) (SEQ ID NO:82) and of 40 cycles of 98° C. for 10 seconds and 68° C. for 8 minutes by using cHAC-F3 (5′-tgcaggtgaagtgacggccagccaagaaca-3′) (SEQ ID NO:83) and cHAC-R3 (5′-tggcagcagggtgacagggaaggcagggaaaag-3′) (SEQ ID NO:84) as primers.

In the above, clone CH2D2 was identified as a positive clone which maintained the CH2D fragment. FIGS. 15 and 16 illustrate an outline of a method for constructing a CH2D fragment by modifying the human chromosome 14 in a DT 40 cell.

(2) Construction of KSL-HACΔ in a DT40 Hybrid Cell

KSL-HAΔ was constructed in a DT40 hybrid cell in the same manner as KSL-HAC in Example 2(5). SLKD17 or SLKD18 comprising the hyg^r cassette in Example 2(4) and the 14D1 comprising the bs^r cassette in Example 3(1) were fused by using PEG1500 (Roche) to construct a DT40 hybrid cell.

The colony was maintained in the presence of hygromycin B (1.5 mg/ml, Invitrogen) and blasticidin S (20 μg/ml, Invitrogen) for 3 weeks to select a cell comprising both of SLKH and 14D fragments. A genomic DNA was extracted from the resistant colony and was subjected to PCR.

It was confirmed by PCR using the following primer combinations whether the SLKH fragment was maintained. That is, primer combinations of IGKC-F and IGKC-R, IGKV-F and IGKV-R, RPIA-F and RPIA-R, EIF2AK3-F and EIF2AK3-R, cos138KO-F and cos138KO-R, CAGpuro-F3 and CAGpuro-R3, 553P-F and 553P-R, hVpreB1-F and hVpreB1-R, hVpreB3-F and hVpreB3-R, IgL-F and IgL-R, 344-F and 344-R, hL5-F and hL5-R, 350P-F and 350P-R, and 553KO-F and 553 KO-R [all described in Example 2(3)] were used.

It was confirmed whether the 14D fragment was maintained, by PCR under conditions of 40 cycles of 98° C. for 10 seconds, 60° C. for 30 seconds, and 72° C. for 1 minute by using the following primer combinations; CAGpuro-F3 and CAGpuro-R3 [Example 2(3)], 14CENKO-F3 and 14CENKO-R3[Example 3(1)], RNR2-1 and STOP-3, VH3-F and VH3-R, g1(g2)-F and g1(g2)-R, CH3-F3 and CH4-R2 [Example 2(5)], and SC355F3R3KO-F2 (5′-gccattgtcgagcaggtagt-3′) (SEQ ID NO:85) and SC355F3R3KO-R2 (5′-tccctcatcagccatcctaa-3′) (SEQ ID:86).

Further, it was confirmed that two human chromosome fragments had an appropriate size (the SLKH fragment was about 156 Mb and the 14D fragment was about 21 Mb) by FISH using the Human Cot-1 DNA (Invitrogen) as a probe.

In the above, clones KSLD1 and KSLD16 were identified as positive clones.

In order to induce a site specific recombination between two loxP sites arranged on the cos 138 site of the SLKH fragment and the RNR2 gene locus of the 14D fragment, respectively, a Cre expression plasmid was introduced into KSLD1 and KSLD16 by electroporation (550 V, 25 μF) according to the description in Example 2(5).

Since the GFP expression was imparted by the PGK promoter-loxP-GFP cassette formed at the translocation site, GFP positive cells were sorted by using FACSAria according to a method described in the publication (Kuroiwa et al., Nat. Biotechnol. 18: 1086-1090, 2000), and recombinants were concentrated.

Two GFP expression positive groups having different expression levels were obtained by carrying out the sorting twice. As a result of analysis by using the PCR primers PGK2 and GFP2 described in Example 2(5), it was confirmed that the group having a lower GFP expression level has a structure in which a desired translocation was occurred, and thus the group was identified as a group maintaining KSL-HACΔ.

In the above, it was confirmed that KSLD1-derived KSLDH1(2L) and KSLD16-derived KSLDH16(2L) were DT40 hybrid cell lines consisting of cell groups which maintained KSL-HACΔ and exhibited a low GFP expression level.

(3) Transfer of KSL-HACΔ from a DT40 Hybrid Cell to a CHO Cell by MMCT and WCF

KSL-HACΔ described in Example 3(2) was transferred from the DT40 hybrid cell line KSLDH1(2L) or KSLDH16(2L) to the CHO cell by using the MMCT method or WCF method.

As for the MMCT method, micronuclei purified from KSLDH1(2L) or KSLDH16(2L) were fused with 2×10⁷ of CHO cells by using PEG1500 (Roche), and selection was carried out by Zeocin (800 μg/ml, Invitrogen) and Ouabain (10⁻⁵ mol/L, Sigma) for 3 weeks.

As for the WCF method, 2×10⁷ of KSLDH1(2L) or KSLDH16(2L) were fused with 2×10⁷ of CHO cells by using PEG1500 (Roche), and selection was carried out by Zeocin (800 μg/ml, Invitrogen) and Ouabain (10⁻⁵ mol/L, Sigma) for 3 weeks.

After Zeocin resistant colonies were harvested, a genomic DNA was extracted and was subjected to PCR screening.

It was confirmed by using the following PCR primer combinations whether KSL-HACΔ was maintained. That is, a combination of IGKC-F and IGKC-R, a combination of IGKV-F and IGKV-R, a combination of RPIA-F and RPIA-R, a combination of EIF2AK3-F and EIF2AK3-R, a combination of cos138KO-F and cos138KO-R, a combination of CAGpuro-F3 and CAGpuro-R3, a combination of 553P-F and 553P-R, a combination of hVpreB 1-F and hVpreB1-R, a combination of hVpreB3 -F and hVpreB3 -R, a combination of IgL-F and IgL-R, a combination of 344-F and 344-R, a combination of hL5-F and hL5-R, a combination of 350P-F and 350P-R, and a combination of 553KO-F and 553 KO-R [all described in Example 2(3)], and a combination of 14CENKO-F3 and 14CENKO-R3 [Example 3(1)], a combination of VH3-F and VH3-R, a combination of g1(g2)-F and g1(g2)-R, a combination of CH3-F3 and CH4-R2, and a combination of PGK2 and GFP2 [all described in Example 2(5)], and a combination of SC355F3R3KO-F2 and SC355F3R3 KO-R2 [Example 3(2)] were used.

Further, it was confirmed by FISH using the Human Cot-1 DNA (Invitrogen) as a probe whether KSL-HACΔ was maintained. The IgH, Igκ, and Igλ gene loci on KSL-HACΔ HACΔ were confirmed by a three-color FISH using the BAC clones RP11-417 P24, RP11-316G9, and RP11-22M5 described in Example 2(6).

Finally, a CGH analysis was carried out with Roche NimbleGen by the custom-made array described in Example 2(6). As a result, it was suggested that there is a homologous structure between clone KSLDC1 obtained by WCF of KSLDH1(2L) and clone KSLDC25 obtained by MMCT of KSLDH16(2L).

Example 4

Construction of the cKSL-HACΔ

(1) Construction of the cKSL-HACΔ in a DT40 Hybrid Cell

In the same manner as KSL-HACΔ in Example 3(2), cKSL-HACΔ was constructed in a DT40 hybrid cell.

SLKD17 or SLKD18 comprising the hyg^r cassette in Example 2(4) and the CH2D-4 comprising the bs^r cassette in Example 3(1) were fused by using PEG1500 (Roche) to construct a DT40 hybrid cell.

The colony was maintained in the presence of hygromycin B (1.5 mg/ml, Invitrogen) and blasticidin S (20 μg/ml, Invitrogen) for 3 weeks to select a cell maintaining both of the SLKH fragment and the CH2D fragment. A genomic DNA was extracted from the colony and was subjected to PCR.

It was confirmed by PCR using the following primers whether the SLKH fragment was maintained. That is, a combination of IGKC-F and IGKC-R, a combination of IGKV-F and IGKV-R, a combination of RPIA-F and RPIA-R, a combination of EIF2AK3-F and EIF2AK3-R, a combination of cos138KO-F and cos138KO-R, a combination of CAGpuro-F3 and CAGpuro-R3, a combination of 553P-F and 553P-R, a combination of hVpreB1-F and hVpreB1-R, a combination of hVpreB3-F and hVpreB3-R, a combination of IgL-F and IgL-R, a combination of 344-F and 344-R, a combination of hL5-F and hL5-R, a combination of 350P-F and 350P-R, and a combination of 553KO-F and 553 KO [all described in Example 2(3)] were used.

It was confirmed by PCR using the following primers whether the CH2D fragment was maintained. That is, a combination of CAGpuro-F3 and CAGpuro-R3 [Example 2(3)], a combination of RNR2-1 and STOP-3, a combination of VH3-F and VH3-R, a combination of g1(g2)-F and g1(g2)-R [all described in Example 2(5)], a combination of 14CENKO-F3 and 14CENKO-R3, a combination of CH25′-F and CH25′-R, a combination of cHAC-F3 and cHAC-R3 [all described in Example 3(1)], and a combination of SC355F3R3KO-F2 and SC355F3R3KO-R2 [Example 3(2)] were used.

Further, it was confirmed by FISH using the Human Cot-1 DNA (Invitrogen) as a probe that two human chromosome fragments had an appropriate size (the SLKH fragment was about 156 Mb and the CH2D fragment was about 21 Mb).

In the above, clones cKSLD2 and cKSLD22 were identified as positive clones.

In order to induce a site specific recombination between two loxP sites arranged on the cos138 site of the SLKH fragment [Example 2(5)], respectively, and the RNR2 gene locus of the CH2D fragment [Example 3(1)] to delete the CAG promoter-zeo^r cassette [Example 3(1)] inserted between the loxP sequences on the chimeric Igμ gene locus, a Cre expression vector was introduced into cKSLD2 and cKSLD22 by electroporation (550 V, 25 μF).

Since the GFP expression capability was imparted by the PGK promoter-loxP-GFP cassette formed at the translocation site, GFP positive cells were sorted by using FACSAria according to a method described in the publication (Kuroiwa et al., Nat. Biotechnol. 18: 1086-1090, 2000), and recombinants were concentrated.

Sorting was carried out twice to obtain a GFP positive cell group having two different GFP expression levels in the same manner as Example 3(2).

It was confirmed by PCR of 40 cycles of 98° C. for 10 seconds and 68° C. for 4 minutes by using the PCR primers PGK2 and GFP2 in Example 2(5) and the PCR primers CreCAGzeo-F3 (5′-gccctcaccttgcagaccacctccatcat-3′) (SEQ ID NO:87) and CreCAGZeo-R3 (5′-cctctcctgctcagtccccttccttccatc3′) (SEQ ID NO:88) that the CAG promoter-zeo^r cassette on the chimeric Igμ gene locus was deleted, and thus it was suggested that a group having a low GFP expression level maintained cKSL-HACΔ which occurred a desired translocation.

In the above, it was confirmed that cKSLD2-derived cKSLDH2(2L) and cKSLD22-derived cKSLDH22(2L) were identified as DT40 hybrid cell lines consisting of cell groups which maintained cKSL-HACΔ and exhibited a low GFP expression level. FIG. 17 illustrates an outline of a method for constructing cKSL-HACΔ in a DT40 hybrid cell.

(2) Transfer of cKSL-HACΔ from a DT40 Hybrid Cell to a CHO Cell by MMCT Method

In the same manner as KSL-HACΔ in Example 3(3), cKSL-HACΔ described in Example 4(1) was transferred from the DT40 hybrid cell line cKSLDH2(2L) or cKSLDH22(2L) to the CHO cell by the MMCT method.

Micronuclei purified from cKSLDH2(2L) or cKSLDH22(2L) were fused with 2×10⁷ of CHO cells by using PEG1500 (Roche), and a selection was carried out by Zeocin (800 μg/ml, Invitrogen) and Ouabain (10⁻⁵ M, Sigma) for 3 weeks.

After Zeocin resistant colonies were harvested, a genomic DNA was extracted, and was subjected to PCR screening. It was confirmed by using the following PCR primers whether cKSL-HACΔ was maintained. That is, a combination of IGKC-F and IGKC-R, a combination of IGKV-F and IGKV-R, a combination of RPIA-F and RPIA-R, a combination of EIF2AK3-F and EIF2AK3-R, a combination of cos138KO-F and cos138KO-R, a combination of CAGpuro-F3 and CAGpuro-R3, a combination of 553P-F and 553P-R, a combination of hVpreB1-F and hVpreB1-R, a combination of hVpreB3-F and hVpreB3-R, a combination of IgL-F and IgL-R, a combination of 344-F and 344-R, a combination of hL5-F and hL5-R, a combination of 350P-F and 350P-R, and a combination of 553KO-F and 553 KO-R [all described in Example 2(3)], a combination of VH3-F and VH3-R, a combination of g1(g2)-F and g1(g2)-R, and a combination of PGK2 and GFP2 [all described in Example 2(5)], a combination of 14CENKO-F3 and 14CENKO-R3, a combination of CH25′-F and CH25′-R, and a combination of cHAC-F3 and cHAC-R3 [all described in Example 3(1)], a combination of SC355F3R3KO-F2 and SC355F3R3KO-R2 [Example 3(2)], and a combination of CreCAGzeo-F3 and CreCAGzeo-R3 [Example 4(1)] were used.

Further, it was confirmed by FISH using the Human Cot-1 DNA (Invitrogen) as a probe whether cKSL-HACΔ was maintained. In addition, the presence of the IgH, and Igλ gene loci on cKSL-HACΔ was confirmed by a three-color FISH using the BAC clones RP11-417P24, RP11-316 G9, and RP11-22M5 described in Example 2(6).

A CGH analysis was carried out with Roche NimbleGen by the custom-made array described in Example 2(6). As a result, it was revealed that clone cKSLDC6 obtained from cKSLD2(2L) by the MMCT method and clones cKSLDC15 and cKSLDC23 obtained from cKSLDH22(2L) by the MMCT method had a homologous structure.

Example 5

Transfer of the HAC into a Bovine Cell Line for Generation of a HAC Bovine for Production of Human IgG

Each of KSL-HAC, KSL-HACΔ, and cKSL-HACΔ was transferred from DT40 hybrid cells to CHO cells by the MMCT method (Kuroiwa et al., Nat Biotechnol. 18: 1086-1090, 2000). The CHO clone comprising the HAC was cultured in F12 medium (Gibco) supplemented with 10% FBS (Gibco) and 0.8 mg/ml of Zeocin under conditions of 37° C. and 5% CO₂.

A HAC-comprising clone was expanded in culture in 12 of T25 flasks. After the cell density reached 80 to 90%, colcemid (Sigma) was added to the medium to give a final concentration of 0.1 μg/ml.

After 3 days, the medium was exchanged with a DMEM medium (Invitrogen) supplemented with 10 μg/ml of cytochalasin B (Sigma). Micronuclei were recovered by centrifuging the flask at 8000 rpm for 60 minutes. The micronuclei were purified through 8-, 5-, and 3-μm filters (Costar), followed by resuspension in a DMEM medium. The obtained micronuclei were used for fusion with bovine fibroblasts as described below.

Bovine fetal fibroblasts (IGHM^−/31IGHML1^−/−, Kuroiwa et al., Nat Biotechnol. 27: 173-181, 2009) were cultured in α-MEM (Invitrogen) medium supplemented with 15% FBS (Hyclone) under conditions of 38.5° C. and 6.5% CO₂. The fibroblasts were expanded in culture in a T175 flask. When the cell density reached 70 to 80%, the cells were detached from the flask with 0.05% trypsin. The fibroblast cells were washed twice with a DMEM medium and then overlayed on the micronuclei suspension.

After the micronuclei-fibroblast suspension was centrifuged at 1,500 rpm for 5 minutes, PEG1500 (Roche) was added to the pellet according to the attached protocol to allow the micronuclei to be fused with the bovine fibroblasts.

Subsequently, the fused cells were plated into ten 24-well plates and cultured in an α-MEM medium supplemented with 15% FBS for 24 hours. After that, the medium was exchanged with a medium containing 0.6 mg/ml of Zeocin.

After being cultured in the presence of antibiotic materials for about two weeks, drug-resistant fused cells were selected.

The selected fused cells comprising various HACs were used as a chromatin donor, and thus a bovine comprising various HACs was produced by a chromatin transfer method described in WO2002/051997.

Example 6

Evaluation of the Human IgG Level in HAC Bovine Serum

The human IgG levels in various HAC bovine sera constructed were measured by a method described in the publication (Kuroiwa et al., Nat Biotechnol. 27: 173-181, 2009). The total amount of the human IgG in each serum of 6-month-old HAC bovines is shown in the following FIG. 18. Further, the average value of the total amount of the human IgG in various 6-month-old HAC bovine sera is shown in the following Table 4.

TABLE 4
Total Amount of the Human IgG in Bovine Serum of
Various 6-Month-Old HAC Bovines (μg/mL)
κHAC	KSL-HAC	cKSL-HACΔ
433.9	1662	4172

As shown in FIG. 18 and Table 4, the amount of human IgG production in serum in bovines having KSL-HAC and cKSL-HACΔ was significantly increased as compared to bovines having κHAC.

In addition, according to the publication (Kuroiwa et al., Nat Biotechnol. 27: 173-181, 2009), the B cell profile in HAC bovine peripheral blood and lymph node was analyzed by flow cytometry.

As a result, the number of B cells expressing IgM in the cKSL-HACΔ bovine peripheral blood was increased as compared to that in the κIAC bovine peripheral blood. Further, the number of B cells expressing IgM even in the KSL-HAC bovine and the cKSL-HACΔ bovine lymph nodes was increased as compared to the number in the κHAC bovine lymph node.

Example 7

Production of the Human IgG Specific to the Anthrax Protective Antigen (PA) by the HAC Bovines

In order to evaluate that HAC bovines could initiate antigen specific humoral responses against a known single antigen due to human IgG, anthrax protective antigens (PA) were used and reviewed. According to a description in the publication (Kuroiwa et al., Nat Biotechnol. 27: 173-181, 2009), three KSL-HAC/IGHM^−/−IGHML1^−/−bovines (No. 1853, No. 1854, and No. 1857) were immunized with PA and was measured the titer of PA specific human IgG. The results are shown in Table 5.

TABLE 5
Production amount of the PA specific human IgG
in the KSL-HAC bovine (U/mg IgG)
				Fifth
	Second	Third	Fourth	Immuni-
	Immunization	Immunization	Immunization	zation
No. 1853	6690
No. 1854	8177
No. 1857	16858	32143	119708	121125

As shown in Table 5, all HAC bovines produced PA specific human IgG. Further, in No. 1857, whenever the immunization was repeated, the production amount of the PA specific human IgG was increased, and thus 121125 U/mg of IgG was produced at a time point of the fifth immunization.

Example 8

Production of Human IgG Specific to T Cell Surface Membrane Protein Mixture by HAC Bovines

In order to evaluate that HAC bovines could initiate antigen specific humoral responses against an unknown complex antigen due to human IgG, a T cell surface membrane protein mixture (fraction of CEM cell membrane formulation) was used as an antigen and examined.

(1) Culture of CEM Cell

By using A RPMI1640 medium (ATCC) comprising 10% bovine fetal serum (Hyclone), the human T cell line CCRF-CEM (ATCC) was allowed to proliferate in a constant humidity and temperature chamber at 37° C. and 5% CO₂ until the cells in a flask of 225 cm² was confluent (2×10⁶ cells/mL).

Into a 850 cm² roller bottle (Corning) with a bent cap, 500 mL of the RPMI1640 medium containing 10% bovine fetal serum was dispensed and the cells were seeded at a density of 2×10⁵ cells/mL. The roller bottle was put on a roller bottle culturing apparatus (Thermo Scientific) and the cells were cultured for 5 days. In order to recover the CEM cells from the roller bottle, the culture was poured into a 2 L sterilized polypropylene biobottle (Nalgen).

Subsequently, the cells were made into a pellet by centrifugation using a Sorvall RC12BP at 450×g and 2 to 8° C. for 30 minutes. The cell pellet was resuspended into sterilized iced PBS, followed by washing operation twice.

After the final washing, the cell pellet was suspended at a density of 2×10⁸ cells/mL in an iced lysis buffer (20 mM Tris chloride, 10 mM NaCl, and 0.1 mM MgCl₂) comprising 1 mM PMSF (Sigma), various protease inhibitors [1.6 μM Aprotinin, 40 μM Leupeptin, 2 mM AEBSF, 0.1 mM Bestatin, 30 μM E-64, and 20 μM PepstatinA (CalBioChem)], and 25.6 μg/ml DNAseI (Sigma). Then, the cells were immediately freezed in liquid nitrogen. The frozen cells were stored at −80° C. until further use.

(2) Isolation of CEM Cell Membrane by Sucrose Density-Gradient Centrifugation

The frozen CEM cells were melted in a cooling water bath. In order to break up the cell membranes, the CEM cells were subjected to ultrasonication twice to three times in a cooling water bath under conditions of 40 amps and 30 seconds by using an ultra sonic processor (Sonics & Materials).

After the crushed material was injected into the bottom of the lysis buffer in the sterilized ultra clear centrifuge tube with a pipette by using a cooled 41% (w/v) sucrose solution, centrifugation was carried out using an ultracentrifuge of Beckman at 83,000×g (SW 32 Ti rotor) for 1 hour at 4° C. A cloud-like intermediate layer comprising the CEM cell membrane which was formed between the sucrose layer and the lysis buffer layer was recovered and transferred to a polycarbonate ultracentrifuge tube, followed by dilution using a sterilized iced PBS to have a ratio of 1:3.

The CEM membranes were made into a pellet by ultracentrifugation at 80,000×g (70.1 Ti rotor) for 50 minutes at 4° C. After supernatant was carefully removed with a sterilized Pasteur pipette, the CEM membranes were once washed by ultracentrifugation at 4° C. for 50 minutes by using sterilized iced PBS. Finally, the CEM cell membranes were resuspended in PBS.

In order to crush the membrane pellet, the CEM cell membranes were subjected to ultrasonication in a cooling water bath under conditions of 20 amps and 30 seconds by using an ultrasonic processor. The CEM membrane crushed material was stored at −80° C. until further use.

(3) Preimmunization of CEM Membrane

Against three KSL-HAC/IGHM^−/−IGHML1^−/−bovine (No. 1874, No. 1884, No. 1886) and two cKSL-HACΔ/IGHM^−/−IGHML1^−/−bovine (No. 1922, No. 1923), immunization was carried out with a CEM membrane preparation at 3 mg/run.

The CEM membrane preparation was prepared by Montanide ISA 25 adjuvant (Seppic) which was an oil-in-water type emulsion with a saponin-derived immune inducer Quil A (Accurate Chemicals). Bovine was immunized four times at intervals of 4 weeks.

The vaccine was intramuscularly inoculated to the cervical region (2 mL/dose). For measurement of antibody titer, serum samples were collected prior to immunization and on days 10 and 14 after immunization. After blood was allowed to stand still in a serum separation tube to clot, and serum was separated by centrifugation. Further, the serum was dispensed at 0.5 to 1 mL, and freezed and stored until future assay. The titer of anti-CEM antibody was determined by CEM cell specific human IgG ELISA.

(4) CEM Cell Specific ELISA Assay

Four dilution series were prepared by using a 5% membrane Block/PBS (GE Healthcare) buffer from a serum sample. In order to prepare a standard curve, seven-step concentration series which was diluted by 2.5 times from 275 times to 67,139 times were prepared by using a serum with a high titer obtained from a CEM immune animal of which a final titer determined in advance as an authentic preparation and using 5% Membrane Block/PBS.

The inverse number of the final concentration was employed as a unit of titer and a final titer determined in the case of an authentic preparation was defined as 55,000 units. With regard to positive control serum and negative control serum, dilution series were prepared with 5% Membrane Block/PBS and used as an internal standard for confirming the consistency of the assay.

In order to determine the titer of the CEM specific human IgG, 50 μL of samples (authentic preparation serum dilution for correction, positive control serum dilution, negative control serum dilution, and measurement sample serum dilution) were injected in duplicate into a U-shaped bottom 96 well-microplate (Costar), and 50 μL of the CEM cells (4×10⁶ cells/mL) was added thereto.

After the plate was allowed to stand still at 4° C. for 60 minutes, the plate was washed with 100 to 200 μL of PBS three times to remove non-bound proteins. After each washing operation, the plates were subjected to centrifugation at 2850×g for 5 minutes to carefully suck in and remove supernatant from each well. After three washing operations, 100 μL of HRP-labeled donkey anti-human IgG antibody (Jackson Immuno Research) diluted with 5% Membrane Block/PBS buffer by 50,000 times was added to each well to resuspend the cell pellet in a HRP solution.

After the plate was allowed to stand still at 4° C. for 30 minutes, the plate was washed with PBS three times same as above. Finally, the bound anti-CEM antibody was detected by dividing 100 μL/well of the TMB+H₂O₂ matrix mixture solution (KPL) into the plate, and the plate was also allowed to stand still at 25° C. for 15 minutes. After the chromogenic reaction was stopped by 100 μL/well of 10% phosphoric acid, 450 nm was measured by using a microplate reader (Biotek Instruments).

A four-parameter standard curve was prepared from values of seven-step dilution series, and a value of the serum sample was calculated by intrapolation on the curve with Gen5Secure Software. An average titer was calculated by carrying out a dilution assay three to four times for each measurement serum sample.

The result is shown in FIG. 19. After the third antigen administration, it was shown that the antigen specific human IgG in the bovine serum was produced at about 1000 to 2000 U/mg IgG in the KSL-HAC bovine, and at about 550 U/mg IgG in the cKSL-HACΔ bovine among the total human IgG.

REFERENCE EXAMPLE

Reference Example 1

Establishment of Mouse A9 Cell Maintaining Human Chromosome 2, 14, and 22

According to a method described in WO1998/037757, a plasmid pSTneo [Katoh et al., Cell Structure and Function, 12, 575-580, 1987; Japanese Collection of Research Biologicals (JCRB) Bank, Deposit No. VE039] is introduced into a human normal fibroblast HFL-1 (RIKEN Japan Cell Bank, Deposit No. RCB0251) to obtain a transformed cell, followed by cell fusion of the transformed cell with a mouse fibroblast A9 (Oshimura et al., Environmental Health Perspectives, 93, 57-58, 1991; JCRB Cell Bank, Deposit No. JCRB0211) to construct a hybrid cell.

Subsequently, according to a method described in WO1998/037757, micronuclei are prepared from the hybrid cell to be fused with the mouse A9 cell. Each clone comprising desired human chromosome 2, 14, and 22 is identified from obtained clones by genome PCR, genomic Southern Analysis, fluorescence in situ hybridization (FISH), and the like.

Reference Example 2

Construction of the DT40 Hybrid Cell kTL1 Containing a Human Chromosome 2 Fragment

By a micronucleus fusion method described in WO2008/013067, the human chromosome 2 is introduced from the A9 cell comprising the human chromosome 2 obtained in Reference Example 1 into the chicken B cell DT40 (JCRB Cell Bank, Deposit No. JCRB2221).

Subsequently, a telomere sequence is inserted into the CD8A gene locus on the human chromosome 2 by introducing a targeting vector pTELPuroCD8A (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000) into the DT40 hybrid cell by using a telomere truncation method described in WO2008/013067, and the truncation of the chromosome is induced at the insertion site. A DT40 hybrid cell kTL1 comprising a human chromosome 2 which has a deleted region from the CD8A gene locus to the telomere end may be constructed by the manipulation.

Reference Example 3

Construction of the DT40 Hybrid Cell 52-18 Containing the Human Chromosome 22

By a micronucleus fusion method described in WO2008/013067, the human chromosome 22 is introduced from the A9 cell comprising the human chromosome 22 obtained in Reference Example 1 into the chicken B cell DT40 (JCRB Cell Bank, Deposit No. JCRB2221). A DT40 hybrid cell 52-18 comprising the human chromosome 22 may be constructed by the manipulation.

Reference Example 4

Construction of the DT40 Hybrid Cell R56 Containing a Human Chromosome 14 Fragment

According to a description of a report by Kuroiwa et al. (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000), a loxP sequence is inserted into the RNR2 gene locus on the human chromosome 14 by introducing a targeting vector pRNR2loxPbsr (Kuroiwa et al., Nature Biotechnology, 18, 1086-1090, 2000) into a DT40 cell (International Patent Organism Depositary, National Institute of Advanced Industrial Science and Technology (AIST), Deposit No. FERMBP-7583) comprising the human chromosome 14 fragment SC20. The DT40 hybrid cell R56 comprising SC20 which has the loxP sequence at the RNR2 gene locus may be constructed by the manipulation.

Reference Example 5

Construction of the DT40 Hybrid Cell #14/DT40 Containing the Human Chromosome 14

By a micronucleus fusion method described in WO2008/013067, the human chromosome 14 is introduced from the A9 cell comprising the human chromosome 14 obtained in Reference Example 1 into the chicken B cell DT40 (JCRB Cell Bank, Deposit No. JCRB2221). The DT40 hybrid cell #14/DT40 comprising the human chromosome 14 may be constructed by the manipulation.

While the present invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope of the present invention. In this connection, this application is based on a U.S. provisional application filed on Nov. 17, 2009 (U.S. provisional application No. 61/261,935), the entire contents thereof being thereby incorporated by reference.

INDUSTRIAL APPLICABILITY

The present invention provides a human artificial chromosome vector comprising a gene encoding the human antibody heavy chain, a gene encoding the human antibody light chain, and a gene encoding IgM heavy chain constant region derived from a non-human animal; and being capable of producing a human antibody with a higher efficiency when the vector is introduced into an animal. By immunizing the animal produced using a human artificial chromosome vector of the present invention with a desired antigen, a large quantity of human polyclonal antibodies can be supplied.

Claims

1. A human artificial chromosome vector comprising a human antibody heavy chain gene, a human antibody light chain gene, and a human antibody surrogate light chain gene.

2. The human artificial chromosome vector according to claim 1, wherein the human antibody surrogate light chain gene is VpreB gene and λ5 gene.

3. The human artificial chromosome vector according to claim 1, comprising a gene of a non-human animal-derived IgM heavy chain constant region.

4. The human artificial chromosome vector according to claim 3, wherein the gene of the non-human animal-derived IgM heavy chain constant region is derived from bovine IGHM.

5. An animal having the human artificial chromosome vector according to claim 1.

6. A bovine having the human artificial chromosome vector according to claim 3.

7. A method for producing a human antibody, comprising:

administering a target antigen into an animal according to claim 5 to produce and accumulate the human antibody specific to the antigen in serum of the animal, and recovering the human antibody specific to the antigen from the serum.

8. A method for producing a human antibody, comprising:

administering a target antigen into a bovine according to claim 6 to produce and accumulate the human antibody in serum of the bovine, and recovering the human antibody specific to the antigen from the serum.