Melanoma differentiation associated gene - 5 and promoter and uses thereof
The invention provides for an isolated nucleic acid encoding Mda-5 (melanoma differentiation associated gene-5) and an isolated Mda-5 polypeptide. The invention further provides a vector comprising the nucleic acid encoding Mda-5, as well as a host cell comprising the vector. The invention provides an antibody which specifically binds to an Mda-5 polypeptide. The invention further provides a method for determining whether a compound is an inducer of Mda-5 gene expression and assays to determine whether a compound modifies the enzymatic activity of the Mda-5 polypeptide.
This application is a continuation of U.S. Ser. No. 09/515,363, filed Feb. 29, 2000, the contents of which are hereby incorporated by reference.
The invention disclosed herein was made with Government support under National Institutes of Health Chemow Endowment No. CA 74468-01 from the U.S. Department of Health and Human Services. Accordingly, the U.S. Government has certain rights in this invention.
BACKGROUND OF THE INVENTIONThroughout this application, various publications are referenced by author and date within the text. Full citations for these publications may be found listed alphabetically at the end of the specification immediately preceding the claims. All patents, patent applications and publications cited herein, whether supra or infra, are hereby incorporated by reference in their entirety. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art as known to those skilled therein as of the date of the invention described and claimed herein.
Abnormalities in differentiation are common occurrences in human cancers ((1) Fisher and Grant, 1985; (2) Waxman, 1995). Moreover, as cancer cells evolve, ultimately developing new phenotypes or acquiring a further elaboration of preexisting transformation-related properties, the degree of expression of differentiation-associated traits often undergo a further decline. These observations have been exploited as a novel means of cancer therapy in which tumor cells are treated with agents that induce differentiation and a loss of cancerous properties, a strategy called ‘differentiation therapy’ ((2-4) Waxman et al., 1988, 1991; Jiang et al., 1994; Waxman, 1995). In principle, differentiation therapy may prove less toxic than currently employed chemotherapeutic approaches, including radiation and treatment with toxic chemicals. The ability to develop rational schemes for applying differentiation therapy clinically require appropriate in vitro and in vivo model systems for identifying and characterizing the appropriate agent or agents that can modulate differentiation in cancer cells without causing undue toxicity to normal cells.
SUMMARY OF THE INVENTIONThe invention provides for an isolated nucleic acid encoding Mda-5 polypeptide as shown in SEQ ID NO:1. A polypeptide having the sequence shown in SEQ ID NO:2.
The present invention provides for an isolated Mda-5 promoter capable of directing transcription of a heterologous coding sequence positioned downstream therefrom, wherein the promoter is selected from the group consisting of: (a) a promoter comprising the nucleotide sequence shown in SEQ ID NO:3; (b) a promoter comprising a nucleotide sequence functionally equivalent to the nucleotide sequence shown in SEQ ID NO: 3; and (c) a promoter comprising a nucleotide sequence that hybridizes to a sequence complementary to the promoter of (a) or (b) in a Southern hybridization reaction performed under stringent conditions. The invention provides for a host cell comprising the recombinant expression construct as described herein. The invention provides for a method for expressing foreign DNA in a host cell comprising: introducing into the host cell a gene transfer vector comprising an Mda-5 promoter nucleotide sequence operably linked to a foreign DNA encoding a desired polypeptide or RNA, wherein said foreign DNA is expressed. The invention further provides for a method for treating cancer in a subject suffering therefrom which comprises administering to the subject an effective amount of a pharmaceutical composition which comprises a recombinant expression construct comprising: (a) a nucleic acid molecule that encodes a selected polypeptide; and (b) an Mda-5 promoter nucleotide sequence operably linked to the nucleic acid molecule of element (a), wherein the coding sequence will be transcribed and translated when in a host cell to produce the selected polypeptide, and the Mda-5 promoter is heterologous to the coding sequence and a pharmaceutically acceptable carrier.
BRIEF DESCRIPTION OF THE FIGURES
FIGS. 14A-14B: Responsiveness of the mda-5 promoter to various inducers:
The following abbreviations are used herein: Mda-5—Melanoma differentiation associated gene-5, CMV—cytomegalovirus,
The invention provides for an isolated nucleic acid comprising the sequence shown in SEQ ID NO: 1 encoding a Melanoma Differentiation Associated Gene-5 (Mda-5) polypeptide.
In one embodiment, the invention provides for an isolated nucleic acid comprising a derivative of the sequence of SEQ ID NO:1 encoding a polypeptide which is functionally equivalent to Mda-5.
The present invention also provides for a fragment of the isolated nucleic acid aforementioned, wherein the fragment encodes a polypeptide having Mda-5 biological activity.
The invention provides for a nucleic acid which hybridizes to the DNA shown in SEQ ID NO:1 or the complementary strand thereof, wherein the nucleic acid or the complementary strand thereof, encodes a polypeptide having Mda-5 activity.
The invention further provides for a vector comprising any of the nucleic acids described herein. In one embodiment, the vector is a replicable vector, a gene transfer vector, an expression vector, or a vector capable of driving expression of a gene of interest in a host cell.
The invention provides for a host cell comprising the aforementioned vector.
The invention provides a method for identifying a compound as an agonist or antagonist of interferon-β, interferon-α or interferon γ which comprises: (a) contacting a cell with the compound, wherein the cell comprises a nucleic acid having the sequence shown in SEQ ID NO:2, or a functional equivalent thereof, operably linked to a reporter gene; (b) measuring the level of reporter gene expressed by the cell in the presence of the compound; (c) comparing the expression level of the reporter gene measured in step (b) with the expression level of reporter gene measured in the absence of the compound, so as to identify whether the compound is an interferon agonist or antagonist; wherein a higher level of reporter gene expression measured in step (b) is indicative of the compound being an interferon agonist, and wherein a lower level of reporter gene expression measured in step (b) is indicative of the compound being an interferon antagonist.
In one embodiment, the compound is a small organic molecule having a weight of about 5 kilodaltons or less.
In another embodiment, the cell is a HO-1 human melanoma cell.
In another embodiment of the invention, the level of reporter gene expression measured which is indicative of an agonist is from 10 to 1000 fold higher than the level of reporter gene expression measured in the absence of the compound.
In another embodiment of the invention, the reporter gene is luciferase.
The invention provides for an isolated polypeptide having the amino acid sequence shown in SEQ ID NO:2 encoding Mda-5.
The invention also provides for an isolated antibody which specifically binds to the polypeptide having the sequence shown in SEQ ID NO:2.
In one embodiment, the antibody is a monoclonal antibody.
The invention provides for an isolated Mda-5 promoter capable of directing transcription of a heterologous coding sequence positioned downstream therefrom, wherein the promoter is selected from the group consisting of: (a) a promoter comprising the nucleotide sequence shown in SEQ ID NO:3; (b) a promoter comprising a nucleotide sequence functionally equivalent to the nucleotide sequence shown in SEQ ID NO: 3; and (c) a promoter comprising a nucleotide sequence that hybridizes to a sequence complementary to the promoter of (a) or (b) in a Southern hybridization reaction performed under stringent conditions.
In one embodiment, the promoter comprises the nucleotide sequence shown in SEQ ID NO:3.
The invention provides for a recombinant expression construct effective in directing the transcription of a selected coding sequence which comprises: (a) an Mda-5 promoter nucleotide sequence according to claim 15; and (b) a coding sequence operably linked to the promoter, whereby the coding sequence can be transcribed and translated in a host cell, and the promoter is heterologous to the coding sequence.
In one embodiment, the Mda-5 promoter comprises a human Mda-5 promoter.
In another embodiment, the human Mda-5 promoter comprises the nucleotide sequence shown in SEQ ID NO:3.
In another embodiment, the coding sequence encodes a tumor suppressor polypeptide.
In another embodiment, the tumor suppressor polypeptide is p21, retinoblastoma protein or p53.
The invention provides for a host cell comprising the recombinant expression construct described herein. In one embodiment the host cell is stably transformed with the recombinant expression construct.
In another embodiment, the host cell is a tumor cell.
In another embodiment, the host cell is a melanocyte.
In another embodiment, the cell is an immortalized cell.
In another embodiment, the tumor cell is a melanoma cell, a neuroblastoma cell, an astrocytoma cell, a glioblastomoa multifore cell, a cerival cancer cell, a breast cancer cell, a lung cancer cell or a prostate cancer cell.
The invention provides for an isolated Mda-5 promoter capable of directing the transcription of a heterologous coding sequence positioned downstream therefrom, wherein the promoter is selected from the group consisting of (a) a promoter comprising the nucleotide sequence shown in SEQ ID NO:3; (b) a promoter comprising a nucleotide sequence functionally equivalent to the promoter in element (a); and (c) a promoter comprising a nucleotide sequence that hybridizes to a sequence complementary to the promoter of element (a) or element (b) in a Southern hybridization reaction performed under stringent conditions.
The invention also provides for a method for treating cancer in a subject suffering therefrom which comprises administering to the subject an effective amount of a pharmaceutical composition which comprises a recombinant expression construct comprising:
-
- (a) a nucleic acid molecule that encodes a polypeptide of interest; and
- (b) an Mda-5 promoter nucleotide sequence operably linked to the nucleic acid molecule of element (a), and wherein the Mda-5 promoter is heterologous to the nucleic acid molecule,
- and a pharmaceutically acceptable carrier.
In one embodiment, the cancer is melanoma, neuroblastoma, astrocytoma, glioblastoma multiforme, cervical cancer, breast cancer, colon cancer, prostate cancer, osteoscarcoma, or chrondosarcoma.
In one embodiment, the cancer is a cancer of the central nervous system of the subject.
In one embodiment, the administering is carried out via injection, oral administration, topical administration, adenovirus infection, liposome-mediated transfer, topical application to the cells of the subject, or microinjection.
In one embodiment, the carrier is an aqueous carrier, a liposome, or a lipid carrier.
The practice of the present invention will employ, unless otherwise indicated, conventional techniques of molecular biology, microbiology, virology, recombinant DNA technology, and immunology, which are within the skill of the art. Such techniques are explained fully in the literature. See, e.g., Sambrook, Fritsch & Maniatis, Molecular Cloning: A Laboratory Manual, Second Edition (1989); DNA Cloning, Vols. I and II (D. N. Glover ed. 1985); Oligonucleotide Synthesis (M. J. Gait ed. 1984); Nucleic Acid Hybridization (B. D. Hames & S. J. Higgins eds. 1984); Animal Cell Culture (R. K. Freshney ed. 1986); Immobilized Cells and Enzymes (IRL press, 1986); Perbal, B., A Practical Guide to Molecular Cloning (1984); the series, Methods In Enzymology (S. Colowick and N. Kaplan eds., Academic Press, Inc.); and Handbook of Experimental Immunology, Vols. I-IV (D. M. Weir and C. C. Blackwell eds., 1986, Blackwell Scientific Publications).
As used in this specification and the appended claims, the singular forms “a,” “an” and “the” include plural references unless the content clearly dictates otherwise.
The present invention provides for an isolated Mda-5 promoter capable of directing transcription of a heterologous coding sequence positioned downstream therefrom, wherein the promoter is selected from the group consisting of: (a) a promoter comprising the nucleotide sequence shown in SEQ ID NO: 3; (b) a promoter comprising a nucleotide sequence functionally equivalent to the nucleotide sequence shown in SEQ ID NO: 3; and (c) a promoter comprising a nucleotide sequence that hybridizes to a sequence complementary to the promoter of (a) or (b) in a Southern hybridization reaction performed under stringent conditions.
In one embodiment of the invention, the promoter comprises the nucleotide sequence shown in SEQ ID NO: 3.
The present invention also provides for a recombinant expression construct effective in directing the transcription of a selected coding sequence which comprises:
(a) an Mda-5 promoter nucleotide sequence as described herein; and
(b) a coding sequence operably linked to the promoter, whereby the coding sequence can be transcribed and translated in a host cell, and the promoter is heterologous to the coding sequence. In another embodiment of the invention, the Mda-5 promoter comprises a human Mda-5 promoter.
In another embodiment of the invention, the human Mda-5 promoter comprises the nucleotide sequence shown in SEQ ID NO:3.
In another embodiment of the invention, the coding sequence encodes a tumor suppressor polypeptide.
In another embodiment of the invention, the tumor suppressor polypeptide is p21, retinoblastoma protein or p53.
The invention provides for a host cell comprising the recombinant expression construct as described herein.
In another embodiment of the invention, the host cell is stably transformed with the recombinant expression construct described herein.
In another embodiment of the invention, the host cell is a tumor cell.
In another embodiment of the invention, the host cell is a melanocyte.
In another embodiment of the invention, the cell is an immortalized cell.
In another embodiment of the invention, the tumor cell is a melanoma cell, a neuroblastoma cell, an astrocytoma cell, a glioblastomoa multifore cell, a cerival cancer cell, a breast cancer cell, a lung cancer cell or a prostate cancer cell.
The invention provides for a method for expressing foreign DNA in a host cell comprising: introducing into the host cell a gene transfer vector comprising an Mda-5 promoter nucleotide sequence operably linked to a foreign DNA encoding a desired polypeptide or RNA, wherein said foreign DNA is expressed.
In another embodiment of the invention, the gene transfer vector encodes and expresses a reporter molecule.
In another embodiment of the invention, the reporter molecule is selected from the group consisting of beta-galactosidase, luciferase and chloramphenicol acetyltransferase.
In another embodiment of the invention, the “introducing” is carried out by a means selected from the group consisting of adenovirus infection, liposome-mediated transfer, topical application to the cell, and microinjection.
The invention provides for an isolated Mda-5 promoter capable of directing the transcription of a heterologous coding sequence positioned downstream therefrom, wherein the promoter is selected from the group consisting of (a) a promoter comprising the nucleotide sequence shown in SEQ ID NO:3; (b) a promoter comprising a nucleotide sequence functionally equivalent to the promoter in element (a); and (c) a promoter comprising a nucleotide sequence that hybridizes to a sequence complementary to the promoter of element (a) or element (b) in a Southern hybridization reaction performed under stringent conditions.
The invention further provides for a method for treating cancer in a subject suffering therefrom which comprises administering to the subject an effective amount of a pharmaceutical composition which comprises a recombinant expression construct comprising: (a) a nucleic acid molecule that encodes a selected polypeptide; and
(b) an Mda-5 promoter nucleotide sequence operably linked to the nucleic acid molecule of element (a), wherein the coding sequence will be transcribed and translated when in a host cell to produce the selected polypeptide, and the Mda-5 promoter is heterologous to the coding sequence and a pharmaceutically acceptable carrier.
In another embodiment of the invention, the cancer is melanoma, neuroblastoma, astrocytoma, glioblastoma multiforme, cervical cancer, breast cancer, colon cancer, prostate cancer, osteoscarcoma, or chrondosarcoma.
In another embodiment of the invention, the cancer is a cancer of the central nervous system of the subject.
In another embodiment of the invention, the administering is carried out via injection, oral administration, or topical administration.
In another embodiment of the invention, the carrier is an aqueous carrier, a liposome, or a lipid carrier.
A method for determining whether a compound is an inducer of Mda-5 gene expression in a cell and an inducer of terminal differentiation of such cell which comprises: (a) contacting a cell with the compound, wherein the cell comprises a nucleic acid encoding Mda-5 having the sequence shown in SEQ ID NO:1, or a functional equivalent thereof, operably linked to an Mda-5 promoter; (b) measuring the level of either (i) Mda-5 mRNA produced or (ii) Mda-5 polypeptide expressed by the cell in the presence of the compound; (c) comparing the expression level of Mda-5 mRNA or polypeptide measured in step (b) with the level measured in the absence of the compound, so as to determine whether the compound is an inducer of Mda-5 gene expression and an inducer of terminal differentiation of the cell.
A method for treating cancer in a subject suffering therefrom which comprises administering to the subject an effective amount of a compound identified by the method of identifying an inducer of Mda-5 gene expression described herein and a pharmaceutically acceptable carrier, so as to induce terminal differentiation of the cancer cells in the subject and thereby treat the cancer.
Definitions
As used herein “therapeutic gene” means DNA encoding an amino acid sequence corresponding to a functional protein capable of exerting a therapeutic effect on cancer cells or having a regulatory effect on the expression of a function in cells.
As used herein “nucleic acid molecule” includes both DNA and RNA and, unless otherwise specified, includes both double-stranded and single-stranded nucleic acids. Also included are hybrids such as DNA-RNA hybrids. Reference to a nucleic acid sequence can also include modified bases as long as the modification does not significantly interfere either with binding of a ligand such as a protein by the nucleic acid or Watson-Crick base pairing.
As used herein “Mda-5 promoter” means the promoter having about 1000 base pairs (bp) derived from the 5′ flanking region of the Mda-5 gene as shown in
Mda-5 cDNA (SEQ ID NO:1) and Mda-5 polypeptide (SEQ ID NO:2)
(See also
As used herein “enhancer element” is a nucleotide sequence that increases the rate of transcription of the therapeutic genes or genes of interest but does not have promoter activity. An enhancer can be moved upstream, downstream, and to the other side of a promoter without significant loss of activity.
Two DNA or polypeptide sequences are “substantially homologous” when at least about 80% (preferably at least about 90%, and most preferably at least about 95%) of the nucleotides or amino acids match over a defined length of the molecule. As used herein, “substantially homologous” also refers to sequences showing identity to the specified DNA or polypeptide sequence. DNA sequences that are substantially homologous can be identified in a Southern hybridization, experiment under, for example, stringent conditions, as defined for that particular system. Defining appropriate hybridization conditions is within the skill of the art. See, e.g., Sambrook et al., supra; DNA Cloning, vols I & II, supra; Nucleic Acid Hybridization, supra.
A sequence “functionally equivalent” to a Mda-5 promoter sequence is one which functions in the same manner as the Mda-5 promoter sequence. Thus, a promoter sequence “functionally equivalent” to the Mda-5 promoter described herein is one which is capable of directing transcription of a downstream coding sequence in substantially similar timeframes of expression and in substantially similar amounts and with substantially similar tissue specificity as the Mda-5 promoter.
In general terms, an “analog” is understood to be a functional equivalent of a given substance and can be a substitute for said substance, including as a therapeutic substitute. An analog also can be a structural equivalent. As used herein, a “Mda-5 analog” is a substance that mimics a biological effect induced and/or mediated by Mda-5. Any substance having such mimetic properties, regardless of the chemical or biochemical nature thereof, can be used as a Mda-5 analog herein. As used herein, an Mda-5 analog can be referred to as a “mimic” or a “mimetic”.
A DNA “coding sequence” or a “nucleotide sequence encoding” a particular protein, is a DNA sequence which is transcribed and translated into a polypeptide in vivo or in vitro when placed under the control of appropriate regulatory sequences.
The boundaries of the coding sequence are determined by a start codon at the 5′-(amino) terminus and a translation stop codon at the 3′-(carboxy) terminus. A coding sequence can include, but is not limited to, procaryotic sequences, cDNA from eucaryotic mRNA, genomic DNA sequences from eucaryotic (e.g., mammalian) sources, viral RNA or DNA, and even synthetic nucleotide sequences. A transcription termination sequence will usually be located 3′ to the coding sequence.
DNA “control sequences” refers collectively to promoter sequences, polyadenylation signals, transcription termination sequences, upstream regulatory domains, enhancers, and the like, untranslated regions, including 5′-UTRs and 3′-UTRs, which collectively provide for the transcription and translation of a coding sequence in a host cell.
“Operably linked” refers to an arrangement of nucleotide sequence elements wherein the components so described are configured so as to perform their usual function. Thus, control sequences operably linked to a coding sequence are capable of effecting the expression of the coding sequence. The control sequences need not be contiguous with the coding sequence, so long as they function to direct the expression thereof. Thus, for example, intervening untranslated yet transcribed sequences can be present between a promoter sequence and the coding sequence and the promoter sequence can still be considered “operably linked” to the coding sequence.
A control sequence “directs the transcription” of a coding sequence in a cell when RNA polymerase will bind the promoter sequence and transcribe the coding sequence into mRNA, which is then translated into the polypeptide encoded by the coding sequence.
A cell has been “transformed” by exogenous DNA when such exogenous DNA has been introduced inside the cell membrane. Exogenous DNA may or may not be integrated (covalently linked) into chromosomal DNA making up the genome of the cell. In procaryotes and yeasts, for example, the exogenous DNA may be maintained on an episomal element, such as a plasmid. In eucaryotic cells, a stably transformed cell is generally one in which the exogenous DNA has become integrated into the chromosome so that it is inherited by daughter cells through chromosome replication, or one which includes stably maintained extrachromosomal plasmids. This stability is demonstrated by the ability of the eucaryotic cell to establish cell lines or clones comprised of a population of daughter cells containing the exogenous DNA.
A “heterologous” region of a DNA construct is an identifiable segment of DNA within or attached to another DNA molecule that is not found in association with the other molecule in nature. For example, a sequence encoding a protein other than an Mda-5 is considered a heterologous sequence when linked to an Mda-5 promoter. Similarly, a sequence encoding an Mda gene (i.e., Mda-6, Mda-7) will be considered heterologous when linked to an Mda gene promoter with which it is not normally associated. Another example of a heterologous coding sequence is a construct where the coding sequence itself is not found in nature (e.g., synthetic sequences having codons different from the native gene). Likewise, a chimeric sequence, comprising a heterologous structural gene and a gene encoding an Mda or a portion of an Mda, linked to an Mda promoter, whether derived from the same or a different Mda gene, will be considered heterologous since such chimeric constructs are not normally found in nature. Allelic variation or naturally occurring mutational events do not give rise to a heterologous region of DNA, as used herein.
Vectors
Especially preferred are virus based vectors. In the case of eukaryotic cells, retrovirus or adenovirus based vectors are preferred. Such vectors contain all or a part of a viral genome, such as long term repeats (“LTRs”), promoters (e.g., CMV promoters, SV40 promoter, RSV promoter), enhancers, and so forth. When the host cell is a prokaryote, bacterial viruses, or phages, are preferred. Exemplary of such vectors are vectors based upon, e.g., lambda phage. In any case, the vector may comprise elements of more than one virus.
The resulting vectors are transfected or transformed into a host cell, which may be eukaryotic or prokaryotic.
The gene transfer vector of the present invention may additionally comprise a gene encoding a marker or reporter molecule to more easily trace expression of the vector.
Examples of such reporter molecules which can be employed in the present invention are well-known in the art and include beta-galactosidase (Fowler et al, Proc. Natl. Acad. Sci., USA, 74:1507 (1977)), luciferase (Tu et al, Biochem., 14:1970 (1975)), and chloramphenicol acetyltransferase (Gorman et al, Mol. Cell. Biol., 2:1044-1051 (1982)).
The gene transfer vector may contain more than one gene encoding the same or different foreign polypeptides or RNAS.
The gene transfer vector may be any construct which is able to replicate within a host cell and includes plasmids, DNA viruses, retroviruses, as well as isolated nucleotide molecules. Liposome-mediated transfer of the gene transfer vector may also be carried out in the present invention.
Examples of such plasmids which can be employed in the present invention include pGL3-based plasmids (Promega). An example of such DNA viruses which can be employed in the present invention are adenoviruses.
Adenoviruses have attracted increasing attention as expression vectors, especially for human gene therapy (Berkner, Curr. Top. Microbiol. Immunol., 158:39-66 (1992)).
Examples of such adenovirus serotypes which can be employed in the present invention are well-known in the art and include more than 40 different human adenoviruses, e.g., Ad12 (subgenus A), Ad3 and Ad7 (Subgenus B), Ad2 and Ad5 (Subgenus C), Ad8 (Subgenus D), Ad4 (Subgenus E), Ad40 (Subgenus F) (Wigand et al, In: Adenovirus DNA, Doerfler, Ed., Martinus Nijhoff Publishing, Boston, pp. 408-441 (1986)). Ad5 of subgroup C is the preferred adenovirus employed in the present invention. This is because Ad5 is a human adenovirus about which a great deal of biochemical and genetic information is known, and it has historically been used for most constructions employing adenovirus as a vector. Also, adenoviral vectors are commercially available, e.g., pCA3 (Microbix Biosystems Inc.).
Methods for producing adenovirus vectors are well-known in the art (Berkner et al, Nucleic Acids Res., 11:6003-6020 (1983); van Doren et al, Mol. Cell. Biol., 4:1653-1656 (1984); Ghosh-Choudhury et al, Biochem. Biophys. Res. Commun., 147:964-973 (1987); McGrory et al, Virol., 163:614-617 (1988); and Gluzman et al, In: Eurkaryotic Viral Vectors, Ed. Gluzman, Y. pages 187-192, Cold Spring Harbor Laboratory (1982)).
Functionally Equivalent
Nucleic acid molecules which are “functionally equivalent” to Mda-5 promoter or Mda-5 cDNA retain the functional properties of the Mda-5 cDNA or MDA-5 promoter. The nucleic acid molecule may be a derivative of the Mda-5 cDNA or promoter such that there are substitutions, deletions, insertions or alterations in the nucleotide sequence which do not alter substantially the function of the nucleic acid. For example, a promoter molecule which is a functional equivalent of Mda-5 promoter having such substitutions will still permit the tissue specific expression of a gene of interest operably linked thereto and expressed in an organism. Modification is permitted so long as the derivative molecules retain its increased potency compared to Mda-5 promoter alone and its tissue specificity. A functional equivalent of Mda-5 cDNA will encode a protein which retains substantially the same biological functions which are characteristic of Mda-5.
The promoter of the present invention in one embodiment is operably linked to a gene of interest. Such a gene of interest is preferably a therapeutic gene. Examples of therapeutic genes include suicide genes, envisioned for the treatment of cancer, for example. These are genes sequences the expression of which produces a protein or agent that inhibits tumor cell growth or induces tumor cell death. Suicide genes include genes encoding enzymes, oncogenes, tumor suppressor genes, genes encoding toxins, genes encoding cytokines, or a gene encoding oncostatin. The purpose of the therapeutic gene is to inhibit the growth of or kill cancer cells or produce cytokines or other cytotoxic agents which directly or indirectly inhibit the growth of or kill the cancer cell.
Suitable enzymes include thymidine kinase (TK), xanthine-guanine phosphoribosyltransferase (GPT) gene from E. coli or E. coli cytosine deaminase (CD), or hypoxanthine phosphoribosyl transferase (HPRT).
Suitable oncogenes and tumor suppressor genes include neu, EGF, ras (including H, K, and N ras), p53, Retinoblastoma tumor suppressor gene (Rb), Wilm's Tumor Gene Product, Phosphotyrosine Phosphatase (PTPase), and nm23. Suitable toxins include Pseudomonas exotoxin A and S; diphtheria toxin (DT); E. coli LT toxins, Shiga toxin, Shiga-like toxins (SLT-1, -2), ricin, abrin, supporin, and gelonin.
In one embodiment, the gene of interest is a cytokine. Suitable cytokines include interferons, GM-CSF interleukins, tumor necrosis factor (TNF) (Wong G, et al., Human GM-CSF: Molecular cloning of the complementary DNA and purification of the natural and recombinant proteins. Science 1985; 228:810); WO9323034 (1993); Horisberger M. A., et al., Cloning and sequence analyses of cDNAs for interferon-beta and virus-induced human Mx proteins reveal that they contain putative guanine nucleotide-binding sites: functional study of the corresponding gene promoter. Journal of Virology, 1990 March, 64(3):1171-81; Li Y P et al., Proinflammatory cytokines tumor necrosis factor-alpha and IL-6, but not IL-1, down-regulate the osteocalcin gene promoter. Journal of Immunology, Feb. 1, 1992, 148(3):788-94; Pizarro T. T., et al. Induction of TNF alpha and TNF beta gene expression in rat cardiac transplants during allograft rejection. Transplantation, 1993 August, 56(2):399-404). (Breviario F., et al., Interleukin-1-inducible genes in endothelial cells. Cloning of a new gene related to C-reactive protein and serum amyloid P component. Journal of Biological Chemistry, Nov. 5, 1992, 267(31):22190-7; Espinoza-Delgado I., et al., Regulation of IL-2 receptor subunit genes in human monocytes. Differential effects of IL-2 and IFN-gamma. Journal of Immunology, Nov. 1, 1992, 149(9):2961-8; Algate P. A., et al., Regulation of the interleukin-3 (IL-3) receptor by IL-3 in the fetal liver-derived FL5.12 cell line. Blood, 1994 May 1, 83(9):2459-68; Cluitmans F. H., et al., IL-4 down-regulates IL-2-, IL-3-, and GM-CSF-induced cytokine gene expression in peripheral blood monocytes. Annals of Hematology, 1994 June, 68(6):293-8; Lagoo, A. S., et al., IL-2, IL-4, and IFN-gamma gene expression versus secretion in superantigen-activated T cells. Distinct requirement for costimulatory signals through adhesion molecules. Journal of Immunology, Feb. 15, 1994, 152(4):1641-52; Martinez O. M., et al., IL-2 and IL-5 gene expression in response to alloantigen in liver allograft recipients and in vitro. Transplantation, 1993 May, 55(5):1159-66; Pang G, et al., GM-CSF, IL-1 alpha, IL-1 beta, IL-6, IL-8, IL-10, ICAM-1 and VCAM-1 gene expression and cytokine production in human duodenal fibroblasts stimulated with lipopolysaccharide, IL-1 alpha and TNF-alpha. Clinical and Experimental Immunology, 1994 June, 96(3):437-43; Ulich T. R., et al., Endotoxin-induced cytokine gene expression in vivo. III. IL-6 mRNA and serum protein expression and the in vivo hematologic effects of IL-6. Journal of Immunology, Apr. 1, 1991, 146(7):2316-23; Mauviel A., et al., Leukoregulin, a T cell-derived cytokine, induces IL-8 gene expression and secretion in human skin fibroblasts. Demonstration and secretion in human skin fibroblasts. Demonstration of enhanced NF-kappa B binding and NF-kappa B-driven promoter activity. Journal of Immunology, Nov. 1, 1992, 149(9):2969-76).
The gene of interest is a growth factor in one embodiment. Growth factors include Transforming Growth Factor-alpha (TGF-alpha) and beta (TGF-beta), cytokine colony stimulating factors (Shimane M., et al., Molecular cloning and characterization of G-CSF induced gene cDNA. Biochemical and Biophysical Research Communications, Feb. 28, 1994, 199(1):26-32; Kay A. B., et al., Messenger RNA expression of the cytokine gene cluster, interleukin 3 (IL-3), IL-4, IL-5, and granulocyte/macrophage colony-stimulating factor, in allergen-induced late-phase cutaneous reactions in atopic subjects. Journal of Experimental Medicine, Mar. 1, 1991, 173(3):775-8; de Wit H, et al., Differential regulation of M-CSF and IL-6 gene expression in monocytic cells. British Journal of Haematology, 1994 February, 86(2):259-64; Sprecher E., et al., Detection of IL-1 beta, TNF-alpha, and IL-6 gene transcription by the polymerase chain reaction in keratinocytes, Langerhans cells and peritoneal exudate cells during infection with herpes simplex virus-1. Archives of Virology, 1992, 126(1-4):253-69).
Preferred vectors for use in the methods of the present invention are viral including adenoviruses, retroviral, vectors, adeno-associated viral (AAV) vectors.
The viral vector selected should meet the following criteria: 1) the vector must be able to infect the tumor cells and thus viral vectors having an appropriate host range must be selected; 2) the transferred gene should be capable of persisting and being expressed in a cell for an extended period of time; and 3) the vector should be safe to the host and cause minimal cell transformation. Retroviral vectors and adenoviruses offer an efficient, useful, and presently the best-characterized means of introducing and expressing foreign genes efficiently in mammalian cells. These vectors have very broad host and cell type ranges, express genes stably and efficiently. The safety of these vectors has been proved by many research groups. In fact many are in clinical trials.
Other virus vectors that may be used for gene transfer into cells for correction of disorders include retroviruses such as Moloney murine leukemia virus (MoMuLV); papovaviruses such as JC, SV40, polyoma, adenoviruses; Epstein-Barr Virus (EBV); papilloma viruses, e.g. bovine papilloma virus type I (BPV); vaccinia and poliovirus and other human and animal viruses.
Adenoviruses have several properties that make them attractive as cloning vehicles (Bachettis et al.: Transfer of gene for thymidine kinase-deficient human cells by purified herpes simplex viral DNA. PNAS USA, 1977 74:1590; Berkner, K. L.: Development of adenovirus vectors for expression of heterologous genes. Biotechniques, 1988 6:616; Ghosh-Choudhury G., et al., Human adenovirus cloning vectors based on infectious bacterial plasmids. Gene 1986; 50:161; Hag-Ahmand Y., et al., Development of a helper-independent human adenovirus vector and its use in the transfer of the herpes simplex virus thymidine kinase gene. J Virol 1986; 57:257; Rosenfeld M., et al., Adenovirus-mediated transfer of a recombinant alpha.sub.1-antitrypsin gene to the lung epithelium in vivo. Science 1991; 252:431).
For example, adenoviruses possess an intermediate sized genome that replicates in cellular nuclei; many serotypes are clinically innocuous; adenovirus genomes appear to be stable despite insertion of foreign genes; foreign genes appear to be maintained without loss or rearrangement; and adenoviruses can be used as high level transient expression vectors with an expression period up to 4 weeks to several months. Extensive biochemical and genetic studies suggest that it is possible to substitute up to 7-7.5 kb of heterologous sequences for native adenovirus sequences generating viable, conditional, helper-independent vectors (Kaufman R. J.; identification of the component necessary for adenovirus translational control and their utilization in cDNA expression vectors. PNAS USA, 1985 82:689).
AAV is a small human parvovirus with a single stranded DNA genome of approximately 5 kb. This virus can be propagated as an integrated provirus in several human cell types. AAV vectors have several advantage for human gene therapy. For example, they are trophic for human cells but can also infect other mammalian cells; (2) no disease has been associated with AAV in humans or other animals; (3) integrated AAV genomes appear stable in their host cells; (4) there is no evidence that integration of AAV alters expression of host genes or promoters or promotes their rearrangement; (5) introduced genes can be rescued from the host cell by infection with a helper virus such as adenovirus.
HSV-1 vector system facilitates introduction of virtually any gene into non-mitotic cells (Geller et al. an efficient deletion mutant packaging system for a defective herpes simplex virus vectors: Potential applications to human gene therapy and neuronal physiology. PNAS USA, 1990 87:8950).
Another vector for mammalian gene transfer is the bovine papilloma virus-based vector (Sarver N, et al., Bovine papilloma virus DNA: A novel eukaryotic cloning vector. Mol Cell Biol 1981; 1:486).
Vaccinia and other poxvirus-based vectors provide a mammalian gene transfer system. Vaccinia virus is a large double-stranded DNA virus of 120 kilodaltons (kd) genomic size (Panicali D, et al., Construction of poxvirus as cloning vectors: Insertion of the thymidine kinase gene from herpes simplex virus into the DNA of infectious vaccine virus. Proc Natl Acad Sci USA 1982; 79:4927; Smith et al. infectious vaccinia virus recombinants that express hepatitis B virus surface antigens. Nature, 1983 302:490.)
Retroviruses are packages designed to insert viral genes into host cells (Guild B, et al., Development of retrovirus vectors useful for expressing genes in cultured murine embryonic cells and hematopoietic cells in vivo. J Virol 1988; 62:795; Hock R. A., et al., Retrovirus mediated transfer and expression of drug resistance genes in human hemopoietic progenitor cells. Nature 1986; 320:275).
The basic retrovirus consists of two identical strands of RNA packaged in a proviral protein. The core surrounded by a protective coat called the envelope, which is derived from the membrane of the previous host but modified with glycoproteins contributed by the virus.
Markers and amplifiers can also be employed in the gene transfer vectors of the invention. A variety of markers are known which are useful in selecting for transformed cell lines and generally comprise a gene whose expression confers a selectable phenotype on transformed cells when the cells are grown in an appropriate selective medium. Such markers for mammalian cell lines include, for example, the bacterial xanthine-guanine phosphoribosyl transferase gene, which can be selected for in medium containing mycophenolic acid and xanthine (Mulligan et al. (1981) Proc. Natl. Acad. Sci. USA 78:2072-2076), and the aminoglycoside phosphotransferase gene (specifying a protein that inactivates the antibacterial action of neomycin/kanamycin derivatives), which can be selected for using medium containing neomycin derivatives such as G418 which are normally toxic to mammalian cells (Colbere-Garapin et al. (1981) J. Mol. Biol. 150:1-14). Useful markers for other eucaryotic expression systems, are well known to those of skill in the art.
Infection of cells can be carried out in vitro or in vivo. In vitro infection of cells is performed by adding the gene transfer vectors to the cell culture medium. When infection is carried out in vivo, the solution containing the gene transfer vectors may be administered by a variety of modes, depending on the tissue which is to be infected. Examples of such modes of administration include injection of gene transfer vectors into the skin, topical application onto the skin, direct application to a surface of epithelium, or instillation into an organ (e.g., time release patch or capsule below the skin or into a tumor), oral administration, injection into the cerebro-spinal fluid, intranasal application, application into eye by dropper, etc.
Expression can be amplified by placing an amplifiable gene, such as the mouse dihydrofolate reductase (dhfr) gene adjacent to the coding sequence. Cells can then be selected for methotrexate resistance in dhfr-deficient cells. See, e.g. Urlaub et al. (1980) Proc. Natl. Acad. Sci. USA 77:4216-4220; Rungold et al. (1981) J. Mol. and Appl. Genet. 1:165-175.
The above-described system can be used to direct the expression of a wide variety of procaryotic, eucaryotic and viral proteins, (genes of interest) including, for example, viral glycoproteins suitable for use as vaccine antigens, immunomodulators for regulation of the immune response, hormones, cytokines and growth factors, as well as proteins useful in the production of other biopharmaceuticals.
It may also be desirable to produce mutants or analogs of the proteins of interest. See description of “functionally equivalent” nucleic acids hereinabove. Such mutants or analogs of the proteins of interest in one embodiment are expressed from functionally equivalent nucleic acids of the gene of interest or of Mda-5 cDNA. Mutants or analogs may be prepared by the deletion of a portion of the sequence encoding the protein, by insertion of a sequence, and/or by substitution of one or more nucleotides within the sequence. Techniques for modifying nucleotide sequences, such as site-directed mutagenesis, are well known to those skilled in the art. See, e.g., Sambrook et al., supra; DNA Cloning, Vols. I and II, supra; Nucleic Acid Hybridization, supra.
For purposes of the present invention, it may be desirable to further engineer the coding sequence to effect secretion of the polypeptide from the host organism. This enhances clone stability and prevents the toxic build up of proteins in the host cell so that expression can proceed more efficiently. Homologous signal sequences can be used for this purpose with proteins normally found in association with a signal sequence. Additionally, heterologous leader sequences which provide for secretion of the protein can be added to the constructs. Preferably, processing sites will be included such that the leader fragment can be cleaved from the protein expressed therewith. (See, e.g., U.S. Pat. No. 4,336,246 for a discussion of how such cleavage sites can be introduced). The leader sequence fragment typically encodes a signal peptide comprised of hydrophobic amino acids.
In one embodiment of the invention, a heterologous gene sequence, i.e., a therapeutic gene, is inserted into the nucleic acid molecule of the invention. Other embodiments of the isolated nucleic acid molecule of the invention include the addition of a single enhancer element or multiple enhancer elements which amplify the expression of the heterologous therapeutic gene without compromising tissue specificity.
The transformation procedure used depends upon the host to be transformed. Mammalian cells can conveniently be transformed using, for example, DEAE-dextran based procedures, calcium phosphate precipitation (Graham, F. L. and Van der Eb, A. J. (1973) Virology 52:456-467), protoplast fusion, liposome-mediated transfer, polybrene-mediated transfection and direct microinjection of the DNA into nuclei. Bacterial cells will generally be transformed using calcium chloride, either alone or in combination with other divalent cations and DMSO (Sambrook, Fritsch & Maniatis, Molecular Cloning: A Laboratory Manual, Second Edition (1989)). DNA can also be introduced into bacterial cells by electroporation. Methods of introducing exogenous DNA into yeast hosts typically include either the transformation of spheroplasts or transformation of intact yeast cells treated with alkali cations.
The constructs can also be used in gene therapy or nucleic acid immunization, to direct the production of the desired gene product in vivo, by administering the expression constructs directly to a subject for the in vivo translation thereof. See, e.g. EPA Publication No. 336,523 (Dreano et al., published Oct. 11, 1989). Alternatively, gene transfer can be accomplished by transfecting the subject's cells or tissues with the expression constructs ex vivo and reintroducing the transformed material into the host. The constructs can be directly introduced into the host organism, i.e., by injection (see International Publication No. WO/90/11092; and Wolff et al., (1990) Science 247:1465-1468). Liposome-mediated gene transfer can also be accomplished using known methods. See, e.g., Hazinski et al., (1991) Am. J. Respir. Cell Mol. Biol. 4:206-209; Brigham et al. (1989) Am. J. Med. Sci. 298:278-281; Canonico et al. (1991) Clin. Res. 39:219 A; and Nabel et al. (1990) Science 249:1285-1288. Targeting agents, such as antibodies directed against surface antigens expressed on specific cell types, can be covalently conjugated to the liposomal surface so that the nucleic acid can be delivered to specific tissues and cells for local administration.
Human Gene Therapy and Diagnostic Use of Vector
There are several protocols for human gene therapy which have been approved for use by the Recombinant DNA Advisory Committee (RAC) which conform to a general protocol of target cell infection and administration of transfected cells (see for example, Blaese, R. M., et al., 1990; Anderson, W. F., 1992; Culver, K. W. et al., 1991). In addition, U.S. Pat. No. 5,399,346 (Anderson, W. F. et al., Mar. 21, 1995, U.S. Serial No. 220,175) describes procedures for retroviral gene transfer. The contents of these support references are incorporated in their entirety into the subject application. Retroviral-mediated gene transfer requires target cells which are undergoing cell division in order to achieve stable integration hence, cells are collected from a subject often by removing blood or bone marrow. It may be necessary to select for a particular subpopulation of the originally harvested cells for use in the infection protocol. Then, a retroviral vector containing the gene(s) of interest would be mixed into the culture medium. The vector binds to the surface of the subject's cells, enters the cells and inserts the gene of interest randomly into a chromosome. The gene of interest is now stably integrated and will remain in place and be passed to all of the daughter cells as the cells grow in number. The cells may be expanded in culture for a total of 9-10 days before reinfusion (Culver et al., 1991). As the length of time the target cells are left in culture increases, the possibility of contamination also increases, therefore a shorter protocol would be more beneficial.
This invention provides for the construction of retrovirus vectors containing the Mda-5 cDNA in a replicable gene transfer vector or Mda-5 promoter linked to a gene of interest for use in gene therapy or for diagonistic uses. The efficiency of transduction of these vectors can be tested in cell culture systems.
Uses of the Compositions of the Invention
This invention involves targeting a gene-of-interest to the a cancer cell so that the protein encoded by the gene is expressed and directly or indirectly ameliorate the diseased state.
After infecting a susceptible cell, the transgene driven by a specific promoter in the vector expresses the protein encoded by the gene. The use of the highly specific gene vector will allow selective expression of the specific genes in cancer cells.
In one embodiment, the present invention relates to a process for administering modified vectors into the skin to treat skin cancer or disorders associated with the skin. More particularly, the invention relates to the use of vectors carrying functional therapeutic genes to produce molecules that are capable of directly or indirectly affecting cells in the skin to repair damage sustained by the cells from defects, disease or trauma.
Preferably, for treating cancer or for treating defects, disease or damage of cells in the skin, vectors of the invention include a therapeutic gene or transgenes, for example a gene encoding TK. The genetically modified vectors are administered into the skin to treat defects, disease such as skin cancer by introducing a therapeutic gene product or products into the skin that enhance the production of endogenous molecules that have ameliorative effects in vivo.
The basic tasks in the present method of the invention are isolating the gene of interest, selecting the proper vector vehicle to deliver the gene of interest to the body, administering the vector having the gene of interest into the body, and achieving appropriate expression of the gene of interest. The present invention provides packaging the cloned genes, i.e. the genes of interest, in such a way that they can be injected directly into the bloodstream or relevant organs of patients who need them. The packaging will protect the foreign DNA from elimination by the immune system and direct it to appropriate tissues or cells.
In one embodiment of the invention, the gene of interest (desired coding sequence) is a tumor suppressor gene. The tumor suppressor gene may be p21, RB (retinoblastoma) or p53. One of skill in the art would know of other tumor suppressor genes, Recent U.S. Pat. Nos. 6,025,127 and 5,912,236 are hereby incorporated by reference to more explicitly describe the state of the art as to tumor suppressor genes.
Along with the human or animal gene of interest another gene, e.g., a selectable marker, can be inserted that will allow easy identification of cells that have incorporated the modified retrovirus. The critical focus on the process of gene therapy is that the new gene must be expressed in target cells at an appropriate level with a satisfactory duration of expression.
The methods described below to modify vectors and administering such modified vectors into the skin are merely for purposes of illustration and are typical of those that might be used. However, other procedures may also be employed, as is understood in the art.
Most of the techniques used to construct vectors and the like are widely practiced in the art, and most practitioners are familiar with the standard resource materials which describe specific conditions and procedures. However, for convenience, the following paragraphs may serve as a guideline.
General Methods for Vector Construction
Construction of suitable vectors containing the desired therapeutic gene coding and control sequences employs standard ligation and restriction techniques, which are well understood in the art (see Maniatis et al., in Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, New York (1982)). Isolated plasmids, DNA sequences, or synthesized oligonucleotides are cleaved, tailored, and religated in the form desired.
Site-specific DNA cleavage is performed by treating with the suitable restriction enzyme (or enzymes) under conditions which are generally understood in the art, and the particulars of which are specified by the manufacturer of these commercially available restriction enzymes (See, e.g. New England Biolabs Product Catalog). In general, about 1 μg of plasmid or DNA sequences is cleaved by one unit of enzyme in about 20 μl of buffer solution. Typically, an excess of restriction enzyme is used to insure complete digestion of the DNA substrate.
Incubation times of about one hour to two hours at about 37 degree. C. are workable, although variations can be tolerated. After each incubation, protein is removed by extraction with phenol/chloroform, and may be followed by ether extraction, and the nucleic acid recovered from aqueous fractions by precipitation with ethanol. If desired, size separation of the cleaved fragments may be performed by polyacrylamide gel or agarose gel electrophoresis using standard techniques. A general description of size separations is found in Methods in Enzymology 65:499-560 (1980).
Restriction cleaved fragments may be blunt ended by treating with the large fragment of E. coli DNA polymerase I (Klenow) in the presence of the four deoxynucleotide triphosphates (dNTPs) using incubation times of about 15 to 25 min at 20.degree. C. to 25.degree. C. in 50 mM Tris (pH 7.6) 50 mM NaCl, 6 mM MgCl.sub.2, 6 mM DTT and 5-10.mu.M dNTPs. The Klenow fragment fills in at 5′ sticky ends but chews back protruding 3′ single strands, even though the four dNTPs are present. If desired, selective repair can be performed by supplying only one of the dNTPs, or with selected dNTPs, within the limitations dictated by the nature of the sticky ends. After treatment with Klenow, the mixture is extracted with phenol/chloroform and ethanol precipitated. Treatment under appropriate conditions with S1 nuclease or Bal-31 results in hydrolysis of any single-stranded portion.
Ligations are performed in 10-50 μl volumes under the following standard conditions and temperatures using T4 DNA ligase. Ligation protocols are standard (D. Goeddel (ed.) Gene Expression Technology: Methods in Enzymology (1991)). In vector construction employing “vector fragments”, the vector fragment is commonly treated with bacterial alkaline phosphatase (BAP) or calf intestinal alkaline phosphatase (CIP) in order to remove the 5′ phosphate and prevent religation of the vector. Alternatively, religation can be prevented in vectors which have been double digested by additional restriction enzyme digestion of the unwanted fragments.
Suitable vectors include viral vector systems e.g. ADV, RV, and AAV (R. J. Kaufman “Vectors used for expression in mammalian cells” in Gene Expression Technology, edited by D. V. Goeddel (1991).
Many methods for inserting functional DNA transgenes into cells are known in the art. For example, non-vector methods include nonviral physical transfection of DNA into cells; for example, microinjection (DePamphilis et al., BioTechnique 6:662-680 (1988)); liposomal mediated transfection (Felgner et al., Proc. Natl. Acad. Sci. USA, 84:7413-7417 (1987), Feigner and Holm, Focus 11:21-25 (1989) and Felgner et al., Proc. West. Pharmacol. Soc. 32: 115-121 (1989)) and other methods known in the art.
Administration of Modified Vectors Into Subject
One way to get DNA into a target cell is to put it inside a membrane bound sac or vesicle such as a spheroplast or liposome, or by calcium phosphate precipitation (CaPO.sub.4) (Graham F. and Van der Eb, A., Virology 52:456 1973; Schaefer-Ridder M., et al., Liposomes as gene carriers: Efficient transduction of mouse L cells by thymidine kinase gene. Science 1982; 215:166; Stpyridis J. C., et al., Construction of transferrin-coated liposomes for in vivo transport of exogenous DNA to bone marrow erythroblasts in rabbits. Exp Cell Res 1986; 164:568-572).
A vesicle can be constructed in such a way that its membrane will fuse with the outer membrane of a target cell. The vector of the invention in vesicles can home into the cancer cells.
The spheroplasts are maintained in high ionic strength buffer until they can be fused through the mammalian target cell using fusogens such as polyethylene glycol.
Liposomes are artificial phospholipid vesicles. Vesicles range in size from 0.2 to 4.0 micrometers and can entrap 10% to 40% of an aqueous buffer containing macromolecules. The liposomes protect the DNA from nucleases and facilitate its introduction into target cells. Transfection can also occur through electroporation.
Before administration, the modified vectors are suspended in complete PBS at a selected density for injection. In addition to PBS, any osmotically balanced solution which is physiologically compatible with the subject may be used to suspend and inject the modified vectors into the host.
For injection, the cell suspension is drawn up into the syringe and administered to anesthetized recipients. Multiple injections may be made using this procedure. The viral suspension procedure thus permits administration of genetically modified vectors to any predetermined site in the skin, is relatively non-traumatic, allows multiple administrations simultaneously in several different sites or the same site using the same viral suspension. Multiple injections may consist of a mixture of therapeutic genes.
Survival of the Modified Vectors So Administered
Expression of a gene is controlled at the transcription, translation or post-translation levels. Transcription initiation is an early and critical event in gene expression. This depends on the promoter and enhancer sequences and is influenced by specific cellular factors that interact with these sequences. The transcriptional unit of many prokaryotic genes consists of the promoter and in some cases enhancer or regulator elements (Banerji et al., Cell 27:299 (1981); Corden et al., Science 209:1406 (1980); and Breathnach and Chambon, Ann. Rev. Biochem. 50:349 (1981)).
For retroviruses, control elements involved in the replication of the retroviral genome reside in the long terminal repeat (LTR) (Weiss et al., eds., In: The molecular biology of tumor viruses: RNA tumor viruses, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. (1982)).
Moloney murine leukemia virus (MLV) and Rous sarcoma virus (RSV) LTRs contain promoter and enhancer sequences (Jolly et al., Nucleic Acids Res. 11:1855 (1983); Capecchi et al., In: Enhancer and eukaryotic gene expression, Gulzman and Shenk, eds., pp. 101-102, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y.).
Promoter and enhancer regions of a number of non-viral promoters have also been described (Schmidt et al., Nature 314:285 (1985); Rossi and de Crombrugghe, Proc. Natl. Acad. Sci. USA 84:5590-5594 (1987)).
The present invention provides methods for maintaining and increasing expression of therapeutic genes using a tissue specific promoter.
In addition to using viral and non-viral promoters to drive therapeutic gene expression, an enhancer sequence may be used to increase the level of therapeutic gene expression. Enhancers can increase the transcriptional activity not only of their native gene but also of some foreign genes (Armelor, Proc. Natl. Acad. Sci. USA 70:2702 (1973)).
For example, in the present invention, CMV enhancer sequences are used with the Mda-5 promoter to increase therapeutic gene expression. Therapeutic gene expression may also be increased for long term stable expression after injection using cytokines to modulate promoter activity.
The methods of the invention are exemplified by preferred embodiments in which modified vectors carrying a therapeutic gene are injected intracerebrally into a subject.
The most effective mode of administration and dosage regimen for the molecules of the present invention depends upon the exact location of the melanoma being treated, the severity and course of the cancer, the subject's health and response to treatment and the judgment of the treating physician. Accordingly, the dosages of the molecules should be titrated to the individual subject. The molecules may be delivered directly or indirectly via another cell, autologous cells are preferred, but heterologous cells are encompassed within the scope of the invention.
The interrelationship of dosages for animals of various sizes and species and humans based on mg/m.sup.2 of surface area is described by Freireich, E. J., et al. Cancer Chemother., Rep. 50 (4):219-244 (1966). Adjustments in the dosage regimen may be made to optimize the tumor cell growth inhibiting and killing response, e.g., doses may be divided and administered on a daily basis or the dose reduced proportionally depending upon the situation (e.g., several divided dose may be administered daily or proportionally reduced depending on the specific therapeutic situation).
It would be clear that the dose of the molecules of the invention required to achieve cures may be further reduced with schedule optimization.
ADVANTAGES OF THE INVENTIONThe Mda-5 promoter of the invention exhibits melanocyte tissue specificity. Since the Mda-5 promoter of the invention is tissue-specific it can only be activated in the targeted tissue, i.e., the skin. Therefore, the genes of interest driven by the Mda-5 promoter will be differentially expressed in these cells, minimizing systemic toxicity.
This invention is illustrated in the Experimental Details section which follows. These sections are set forth to aid in an understanding of the invention but are not intended to, and should not be construed to, limit in any way the invention as set forth in the claims which follow thereafter.
EXPERIMENTAL DETAILS Example 1 Melanoma Differentiation Associated Gene-5, Mda-5, a Novel Interferon Inducible Gene with Structural Similarities to RNA Helicases and CARD Motif Containing ProteinsMelanoma differentiation associated gene-5, mda-5, is induced during terminal differentiation in human melanoma cells treated with the combination of recombinant fibroblast interferon (IFN-) and the antileukemic compound mezerein (MEZ). The complete open reading frame of the mda-5 cDNA and its promoter region has now been identified and characterized. Mda-5 encodes a 116.7-kDa protein that contains a caspase recruitment domain (CARD) and an RNA helicase motif. Treatment of HO-1 human melanoma and human skin fibroblast cells with IFN-α, IFN-0, IFN-γ, TNF-α and poly IC induce mda-5 expression. IFN-γ and poly IC are the most potent single inducers of mda-5 expression, resulting in a ≧5-fold higher induction than with other inducers. Induction of mda-5 expression by IFN-β is also apparent in normal and tumor cell lines of diverse origin. Thus, mda-5 is a novel IFN-β-responsive gene. MEZ, which reversibly induces specific markers of differentiation in HO-1 cells, does not induce mda-5 expression, whereas it increases both the level of steady-state mda-5 mRNA and mda-5 RNA transcription. The finding that most organs, except brain and lung, contain low levels of mda-5 transcripts suggest that the biological role of mda-5 may be closely related to its induction by exogenous agents. Nuclear run-on assays indicate that the level of regulation of mda-5 occurs transcriptionally. The half-life of mda-5 following treatment with IFN-β or IFN-β+MEZ is between 5-6 hr, confirming that the primary regulation of mda-5 by these agents occurs by enhanced RNA transcription rates. Isolation and characterization of the promoter region of mda-5, provides further documentation that the primary mode of regulation of this gene involves changes in RNA transcription. MDA-5 protein was detected at the predicted size by in vitro translation and Western blot analysis of transiently expressed fusion proteins. GFP-mda-5 fusion proteins were produced and found to localize in the cytoplasm where mda-5 may effects on mRNA translation, mRNA sequestration and decay of specific messages. Ectopic expression of mda-5 reduces the colony-forming efficiency of HO-1 melanoma cells by ˜70%, which suggests a growth inhibitory or a pro-apoptotic role of mda-5. In these contexts, mda-5 may play a key role in growth inhibition induced by IFN-β and may also function in apoptotic signaling.
Introduction
Abnormalities in differentiation are common occurrences in human cancers ((i) Fisher and Grant, 1985; (2) Waxman, 1995). Moreover, as cancer cells evolve, ultimately developing new phenotypes or acquiring a further elaboration of preexisting transformation-related properties, the degree of expression of differentiation-associated traits often undergo a further decline. These observations have been exploited as a novel means of cancer therapy in which tumor cells are treated with agents that induce differentiation and a loss of cancerous properties, a strategy called differentiation therapy, ((2-4) Waxman et al., 1988, 1991; Jiang et al., 1994; Waxman, 1995). In principle, differentiation therapy may prove less toxic than currently employed chemotherapeutic approaches, including radiation and treatment with toxic chemicals. The ability to develop rational schemes for applying differentiation therapy clinically require appropriate in vitro and in viva model systems for identifying and characterizing the appropriate agent or agents that can modulate differentiation in cancer cells without causing undue toxicity to normal cells.
Treatment of human melanoma cells with a combination of recombinant human fibroblast interferon (IFN-β) and the antileukemic compound mezerein (MEZ) results in a rapid and irreversible suppression of growth and the induction of terminal cell differentiation ((5) Fisher et al., 1985). This process is associated with a number of changes in cellular phenotype and gene expression ((3, 6-7) Jiang et al., 1993, Jiang et al., 1994). To define the molecular basis of terminal differentiation in human melanoma cells subtraction hybridization has been employed ((8) Jiang and Fisher, 1993). In brief, cDNA libraries were prepared from temporal RNA samples obtained from HO-1 human melanoma cells treated with IFN-β+MEZ and control untreated HO-1 cells and control cDNAs were subtracted away from differentiation-inducer treated cDNAs ((8) Jiang and Fisher, 1993). This approach resulted in an enrichment of genes displaying elevated expression as a function of treatment with the different inducers and the induction of irreversible growth suppression and terminal cell differentiation. Screening of the subtracted differentiation inducer treated HO-1 cDNA library identified both known and novel cDNAs displaying elevated expression in differentiation inducer treated HO-1 cells ((3, 6, 8-14) Jiang and Fisher, 1993; Jiang et al., 1994, 1995, 1996; Lin et al., 1994, 1996; Huang et al., 1999a, 1999b). Four classes of genes, called melanoma differentiation associated (mda) genes, have been cloned using this approach ((8) Jiang and Fisher, 1993). These include genes displaying elevated expression as a function of treatment with: IFN-β and IFN-β+MEZ (Type I mda genes); MEZ and IFN-β+MEZ (Type II mda genes); IFN-β, MEZ and IFN-β+MEZ (Type III mda genes); and predominantly with IFN-β+MEZ ((3,8) Jiang and Fisher, 1993; Jiang et al., 1994). This approach has resulted in the cloning of both known and novel genes involved in important cellular processes, including cell cycle control (mda-6/p21), interferon signaling (ISG-15, ISG-54), cancer growth control (mda-7), immune interferon response (mda-9), transcription control (c-jun, jun-B), immune recognition (HLA Class I) and cell membrane processes (α5 integrin, βa integrin, fibronectin) ((3, 8-15) Jiang and Fisher, 1993; Jiang et al., 1994; Jiang et al., 1995a, 1995b, 1996, 1996; Lin et al., 1994, 1996).
Subtraction hybridization initially identified a small EST named mda-5. Expression of mda-5 was elevated in HO-1 cells treated with IFN-β+MEZ and to a lesser extend by IFN β+IFN-γ. A complete mda-5 cDNA has now been cloned and its properties determined. This gene is a novel early IFN responsive gene, whose activity is increased maximally by treatment with IFN-β and dsRNA. Moreover, the combination of IFN-β+MEZ synergistically induces mda-5 expression in HO-1 and additional cell types, both normal and cancer. The protein structure of MDA-5 indicates potential relationships to RNA helicases and genes containing CARD domains. However, based on the structure of the MDA-5 protein this gene may represent a new member of the helicase gene family. Ectopic expression of mda-5 induces growth suppression, as indicated by a reduction in colony formation, in HO-1 human melanoma cells. Identification, cloning and analysis of upstream genomic sequences have confirmed that the mda-5 gene is responsive at a transcriptional to induction primarily by IFN-β and dsRNA. A potential role for mda-5 in growth suppression induced by IFN and as a molecule involved in the cellular defense mechanism against viral infection is suggested.
Materials and Methods
Cell Culture and Treatment Protocol: HO-1 human melanoma cells, early passage human skin fibroblast (purchased from ATCC) and 293T cells were grown in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum at 37° C. in a 5% CO2/95% air humidified incubator. Prior to treatment, cells were refed with fresh medium and exposed to the indicated compound(s) at the concentrations specified in the figure legends.
Cloning and Sequencing of mda-5: The full length of the mda-5 cDNA was cloned by using the complete open reading frame (C-ORF) technology based on the partial mda-5 EST sequence ((16) Kang and Fisher, 2000). Sequencing was performed by the dye-conjugated dideoxy chain termination method. The ORF of mda-5 was cloned into the SmaI site of pcDEF3 in which mda-5 expression was regulated by the EF-1α promoter. Deletion mutant DN7 (D310-484 spanning the ATPase motif) was constructed by ligation of BamHI-StuI fragment with Klenow-filled AlwNI-NotI fragment into pcDEF3. Antisense mda-5 expression vector was constructed by cloning the 1-1830 bp mda-5 cDNA fragment in an antisense orientation into pcDEF3. GFP-mda-5 fusion expression vector was constructed by ligation of the mda-5 cDNA into the SmaI site of pEGFP-C2. The sequences of the expression vectors were verified as described above.
Northern Blot Analyses and Nuclear Run-On Assays: Total cellular RNA samples were prepared by guanidium isothiocyanate/phenol extraction followed by isopropanol precipitation. Ten 10 μg of total RNA were resolved in 1% agarose gels with formaldehyde and were transferred to Nylon membranes. EcoRI fragment of mda-5 cDNA (2.5 kb) was labeled with 32P using a multiprime labeling kit (Boehringer Mannheim) and used to probe the transferred membrane. Nuclear run-on assays were performed as previously described ((17) Su et al., 1993, 1999). Probes used for nuclear run-on assays were prepared by RT-PCR and included the mda-5 5′, 9-837 bp; mda-5 3′, 2531-3365 bp; and GAPDH fragment.
In vitro translation: In vitro translation of mda-5 was performed with Novagen's STP3 kit using T7 RNA polymerase with 35S-Methionine as described in the manufacture's protocol. Template for transcription and translation was prepared by BamH1 digestion followed by phenol/chloroform extraction of pGEM-7Zf(+)-mda-5. Proteins that were in vitro translated were resolved in 9% SDS-PAGE and detected by autofluorography.
Transient Transfection Assays: 293T cells were plated 1 day prior to transfection and grown to ˜70% confluency. For intracellular localization, sterilized cover slips were placed in culture dishes and cells were seeded at 1×105 cells/6 cm tissue culture plate. Transient transfection assays were performed using SuperFect from Qiagen as described in the manufacturer's protocol. Ten μg of supercoiled plasmid DNA was transfected into 10 cm-tissue culture dish and cells were harvested two days after transfection.
Western Blot Analysis and Fluorescent Confocal Microscopy: Protein samples were prepared from transiently transfected cells by lysis in RIPA buffer supplemented with protease inhibitors. Twenty μg of protein was resolved in 9% SDS-PAGE and transferred to nitrocellulose membranes. MDA-5 fusion proteins were probed with either α-HA antibody (Boehringer Mannheim) or α-GFP antibody (ClonTech) and HRP-conjugated anti-Mouse IgG (Sigma) and detected by ECL (Amersham). For Fluorescence microscopy, cover glass containing transfected cells were washed with PBS and mounted onto glass slides with mounting medium. Cells were observed with fluorescent confocal microscopy.
Colony-Forming Assays: HO-1 melanoma cells were plated at 8×105 in a 6-cm dish one day prior to transfection. Five μg of supercoiled expression vector DNA was transfected into cells with SuperFect (Qiagen) as described above (18). Two days after transfection, cells were harvested by trypsinization and replated at 105 cells/6-cm dish with complete medium containing 750 μg G418/ml. From each transfection, three dishes were plated. The G418-containing media was replaced once a week for three week. Cells were stained with Giemsa and colonies containing more than 50 cells were counted.
Results
Cloning and Sequence Analysis of mda-5: Subtraction hybridization between a temporally spaced differentiation inducer, IFN-β+mezerein (MEZ), treated HO-1 human melanoma cDNA library and a temporally spaced untreated control HO-1 cDNA library identified a differentially expressed 0.3 kb EST, melanoma differentiation associated gene-5 (mda-5) ((8) Jiang and Fisher, 1993). Northern blotting analysis indicated that the mda-5 EST hybridized with a mRNA species of ˜3.8 kb in IFN-β+MEZ treated HO-1 cells ((8) Jiang and Fisher, 1993; Jiang et al., 1994). A full length mda-5 cDNA containing the complete open reading frame (ORF) was obtained using the C-ORF technique (
Electronic sequence analysis of the MDA-5 protein using motif and profile scans of proteins presently in the protein database identified two conserved domains, a caspase recruitment domain (CARD) and an RNA helicase domain. The CARD domain which was defined by generalized profile alignment within the RAIDD and ICH-1 amino terminal regions, is present in various apoptotic molecules such as Mch6, ICE, ICH-2, c-IAP1, c-IAP2 and Ced-3. Current evidence suggests that the biological role of CARD is the recruitment of caspase to apoptotic signaling receptor complexes (19). The sequence alignment of N-terminal 50 amino acids (aa 125-174) of MDA-5 with other CARD-proteins reveals significant sequence homology at conserved amino acids of CARD (
RNA nuclear cytosolic transport, translation and viral replication by ATP-dependent unwinding of dsRNA (20). However, based on the unique structure of MDA-5, it is not possible at present to ascribe a biological role for this mew molecule and new family of helicases.
Expression Pattern of mda-5: Since the mda-5 EST was cloned from differentiating HO-1 melanoma cells treated with IFN-β+MEZ, further studies were performed to define the type of molecules capable of regulating mda-5 expression. For this purpose, HO-1 cells were treated with a spectrum of agents affecting growth and differentiation in melanoma cells, including retinoic acid, mycophenolic acid, 12-O-tetradecanoylphobol-13-acetate (TPA) and 3′-5′ cyclic AMP. The effect of different types of IFNs and dsRNA (poly IC) and the effect of growth in serum-free medium on mda-5 expression was also evaluated by Northern blotting analyses. As seen in
The induction of mda-5 expression by IFN-β also occurs in additional human melanoma cells and in normal and tumor cell lines of diverse origin treated with IFN-5 (
Since IFN signals through membrane receptor associated tyrosine kinases, the inducibility of mda-5 in HO-1 melanoma cells by ligands of other membrane tyrosine kinase receptors including IL-6, EGF, TGF-α, TGF-β, TNF-α and PDGF was studied by Northern blotting (
2E Among the other ligands of membrane receptors, TNF-α induced mda-5 expression at comparable levels as seen with IFN-α (
Treatment of HO-1 cells with IFN-β+MEZ results in terminal differentiation and a concomitant irreversible loss in cellular proliferation (Fisher et al., 1985). Terminal differentiation in the majority of inducer-treated cells occurs within 24 hr of treatment. In this context, the timing of mda-5 expression can provide a clue to the involvement of mda-5 in the induction of differentiation or in the maintenance of the differentiated phenotype. The timing of response to treatment can also provide insights into the mechanism of induction of mda-5. The timing of mda-5 expression was studied by Northern blotting and mda-5 message level began increasing within 2 hr of treatment with IFN-D or IFN-β+MEZ (
Organ-Specificity of mda-5 Expression: The organ-specific expression pattern of mda-5 was determined by hybridization of this gene with Poly A+ RNA from different organs immobilized on multiple tissue Northern blots (ClonTech)(
Mechanistic Aspects of mda-5 Induction: Steady state transcript levels of mda-5 were greatly increased during induction of terminal differentiation in HO-1 melanoma cells. The increased mda-5 message level could result from post-transcriptional control, such as message stabilization, or from enhanced transcription. The time course of decay in IFN-β and IFN-β+MEZ induced mda-5 mRNA levels were determined by blocking transcription with actinomycin D. A gradual temporal decrease in mda-5 transcript level after actinomycin D treatment was observed in both IFN-β and IFN-β+MEZ treated cells (
Specific gene expression changes can be altered in response to a signaling event with or without prior protein synthesis. Certain gene expression changes (early response genes) including transcription factors and key signaling molecules do not require protein synthesis prior to their expression. By blocking protein synthesis with cycloheximide, a translation inhibitor, it is possible to determine whether induction of mda-5 expression by appropriate inducer treatment requires or is independent of prior protein synthesis (
Expression of MDA-5 Protein and Intracellular Localization of MDA-5: To verify the authenticity of the mda-5 cDNA clone, in vitro translation experiments were performed. Expression of the mda-5 cDNA in an in vitro translation assay results in an encoded protein of ˜120 kDa, close to the predicted size of the MDA-5 protein which is 116.7 kDa (
Effect of mda-5 on Colony Forming Ability of HO-1 Cells: HO-1 cells treated with IFN-β grow slower and display a noticeable enlargement in size in comparison with untreated cells. Since mda-5 is induced primarily by IFN-β, ectopic expression of mda-5 could mimic the effect IFN-β treatment and decrease proliferation. It is also conceivable that the CARD region of mda-5 could induce apoptotic signals and that ectopic expression of mda-5 could affect cell survival. To test for growth inhibitory or pro-apoptotic effects of mda-5 this gene was transfected and ectopically expressed in HO-1 cells and colony forming ability was determined (
Mda-5 Promoter Isolation and Characterization: Induction of mda-5 mRNA subsequent to treatment of human HO-1 melanoma cells with IFN-β indicated the strong likelihood of transcriptional regulation of gene expression based on Northern blot studies. To determine if the primary level of regulation was indeed transcriptional, a nuclear run-on experiment was performed (
Having confirmed that induction of Mda-5 mRNA occurred primarily at the transcriptional level, it was decided that regulatory genomic DNA sequences involved in this process should be isolated and characterized. To achieve this goal, a human genomic DNA library constructed in a Bacterial Artificial Chromosome vector (BAC, Genome Systems Inc.) was screened using the mda-5 cDNA as a probe. Two rounds of screening were performed to obtain two overlapping clones that spanned the entire mda-5 genomic locus including several thousand bp of sequence upstream of the translational initiation codon. Mapping of the BAC clone containing the upstream region by restriction enzyme digestion, Southern blotting and sequence analysis permitted the identification of DNA fragments that contained potentially important regulatory sequences, which in the case of most protein coding genes lie upstream of the transcription initiation site. An approximately 7 kb HindIII fragment containing a partial first exon (including the initiator methionine) and approximately 6 kb of upstream sequence (
The modified mda-5 reporter construct was transfected into parallel sets of HO-1 cells that were treated or not with IFN-β. Quantitation of luciferase activity indicated that this modified reporter containing a partially deleted Exon 1 and around 6 kb of upstream sequences, showed ˜10 fold higher luciferase activity in cells that had been treated with IFN-β compared to untreated controls. This level of induction was comparable to that seen with the endogenous gene in Northern blot analyses. It therefore appeared that the cloned regulatory genomic DNA sequence in the reporter construct contained the elements required for the regulation of the mda-5 gene. It was however, necessary to confirm that the cloned sequences contained all the regulatory elements involved in the transcriptional control of the endogenous cellular gene. Since HO-1 melanoma cells show a very low and variable transfection efficiency it initially proved very difficult to determine the activity of the transiently transfected reporter in a consistent way for variables such as kinetics of induction, optimal concentration of inducer and the identification of other potential activators. To circumvent this technical problem the mda-5 promoter construct was stably integrated into genomic DNA of HO-1 cells by co-transfection with a puromycin resistance plasmid and selection to isolate a clonal population of stable integrants. This selection procedure resulted in the production of several clones of which 48 were randomly picked for further analysis. Screening of these stable promoter clones by treatment with IFN-β indicated that an entire range from completely inactive to highly active, as measured by luciferase activity, had been obtained (
Discussion
Genes displaying differential expression as a function of induction of terminal differentiation by treatment of HO-1 melanoma cells with IFN-β+MEZ are classified into four subgroups based on their induction pattern (Jiang and Fisher, 1993). Mda-5 represents a Type I mda gene, which is induced by IFN-β and IFN-β+MEZ. Treatment with MEZ alone, which is a protein kinase C activator and a weak second-stage tumor promoter, does not induce mda-5 expression, but it potentiates mda-5 expression at a transcriptional level when combined with IFN-β. The inducible expression of 21-5′oligoadenylate synthetase, another IFN-responsive gene, by IFN-α is augmented by TPA. Numerous evidence based on the use of PKC inhibitors indicate that the potentiation of IFN-gene expression by TPA involved activation of PKC, but the exact mechanism of this induction remains to be determined.
HO-1 melanoma cells treated with IFN-β increase in size, display slower growth kinetics and exhibit enhanced melanogenesis, but they do not undergo obvious morphological changes or cell death (Fisher et al., 1985). In contrast, MEZ, which does not induce mda-5, induces profound changes in the morphology of HO-1 cells, including the production of dendrite-like processes. Reagents that induce specific components of melanocytic differentiation in human melanoma cells, including all trans retinoic acid (RA), mycophenolic acid (MPA), cyclic-AMP (cAMP), dimethyl sulfoxide (DMSO) and TPA, also fail to significantly induce mda-5 expression. Therefore, it is possible that the primary role of mda-5 in the induction of terminal cell differentiation of HO-1 cells by IFN-β+MEZ is restricted to IFN-β-mediated suppression of cell proliferation.
Although IFN-α and IFN-γ significantly induce mda-5 expression, IFN-β was >5-fold more effective in inducing mda-5 expression than either IFN-α or IFN-γ. IFN-β enhanced the expression of mda-5 in normal and tumor cell lines, including various melanoma cell lines regardless of their p53 or Rb status. Although mda-5 was undetectable in Northern blot of whole brain Poly A+ mRNA, mda-5 was detected and further induced by IFN-β treatment in cultured normal cerebellum and glioblastoma multiforme cells. In these contexts, mda-5 can be classified as an IFN-β-inducible gene. Both IFN-β and IFN-α share a common receptor (IFN-R1) and often display a similar pattern of gene expression changes, but the biological effects of these agents can be distinct. Mda-5 and a gene named INF-R1 are unique in that they display increased responsiveness to IFN-β than to IFN-α, which may involve IFN-β-specific cellular processes.
In addition to IFNs, the expression of mda-5 is also induced in both HO-1 melanoma and human skin fibroblast cells by TNF-α and poly IC. Both TNF-α and poly IC are established inducers of IFN-β gene expression. Based on these facts it is possible that TNF-α and poly IC may induce mda-5 gene expression by modulating IFN-β gene expression. In contrast, pretreatment with cycloheximide (CHX), a protein synthesis inhibitor did not inhibit mda-5 expression induced by TNF-α or poly IC, which suggests that these agents are direct inducers of mda-5. Poly IC directly activates PKR (dsRNA-activated interferon-inducible protein kinase) and induces class I MHC expression. TNF-α signaling was also found to be dependent on PKR activation. Alternatively or additionally, PKR which, independent of IFN receptor signaling, phosphorylates IkB and transactivates NFkB could be the mediator of TNF-α and poly IC-induced mda-5 expression. However, it is still possible that TNF-α and poly IC could stimulate secretion of preexisting IFN-β without the requirement of new protein synthesis.
IFNs were initially identified as molecules that provide immediate protection against viral infection by eliciting an antiviral state in treated cells. IFN treatment evokes diverse responses depending on the target cell which include growth inhibition, changes in differentiation, induction or inhibition of apoptosis and changes in the expression of immune system modulating genes. IFN-β displays more potent growth inhibitory effects on normal melanocytes and melanoma cells, including HO-1, than IFN-α and IFN-γ. Interestingly, the growth inhibitory effect of IFNs in these cells correlates well with the level of induction of mda-5 expression. In addition, both inducers of mda-5, TNF-α and poly IC inhibit cell proliferation and induce apoptosis in a cell type specific manner. Induction of mda-5 by IFN-β is an early event, since the steady state mRNA message levels begin increasing within two hr of treatment. These results suggests that mda-5 may play a pivotal role in IFN-β-mediated suppression of cell proliferation.
Ectopic expression of mda-5 reduces the colony-forming capacity of HO-1 melanoma cells by ˜70%. Considering the inefficient nature of transfection and the random incorporation of transfected genes into the cellular genome, the effect of ectopic mda-5 expression on colony-forming efficiency is quite dramatic. Surprisingly, the expression of a deletion mutant of mda-5 (deletion of the ATPase motif) also reduced colony formation (˜47%), but was markedly less potent than the wild type mda-5 gene. Colony-forming efficiency is regulated by multiple parameters including inherent plating efficiency, and the growth inhibitory or toxic effect of the transfected gene product. Further studies are required to determine which factor is most critical in reducing the colony-forming efficiency of cells ectopically expressing mda-5.
Profile scans of the MDA-5 protein reveal putative CARD and RNA helicase motifs. Multiple sequence alignments of the CARD motif in MDA-5 using the ClustalW system indicate that this region most closely resembles the CARD of RAIDD, which is a component of TNF-R1-mediated apoptotic signaling pathway and which contains both a death domain and a CARD motif. RAIDD interacts with RIP through its death domain and with ICH-1 (caspase-2) probably via its CARD motif. Although not as effective as IFN-β, TNF-α also induces mda-5 expression in HO-1 melanoma cells. In is therefore conceivable that mda-5 may interact with RAIDD and serve as a death effector molecule like ICH-1. A pro-apoptotic role of mda-5 is also supported by the dsRNA-dependent induction of this gene, which also activates PKR, a recognized molecule involved in growth suppression and apoptosis. However, a direct apoptotic role of mda-5 does not coincide with the effect of IFN-β on HO-1 melanoma cells, which results in growth suppression and not cell death. It is feasible that mda-5 may be a component of a death effector molecule, but by itself it lacks the capacity to trigger apoptosis. In this context, ectopic expression of mda-S may result in growth inhibition and not apoptosis. It is also possible that the level of ectopic expression of mda-5 may determine whether this molecule is growth inhibitory or toxic. If this is true, expression of mda-5 by means of a adenovirus under the control of a strong promoter may produce sufficiently high levels of MDA-5 to induce cell death as opposed to growth inhibition.
Another distinct motif present in the MDA-5 protein is a RNA helicase signature domain, which spans the C-terminal half of this molecule. RNA helicase is a family of enzymes with a helicase motif, which potentially catalyzes NTP-dependent dsRNA unwinding activity. Not only are the core residues among the RNA helicases conserved, but also the spaces between these residues are retained in the different RNA helicases. Three main features characterize RNA helicases from the N- to C-terminal, an ATPase A motif(GXXGXGKT), an ATPase B motif (DEAD, DEAH or DEXH) and a critical domain for RNA interaction (HRIGRXXR) (Dong-chul, correct?). RNA helicases are classified into three subgroups based on their ATPase B motifs. RNA helicases are implicated in the majority of steps associated with RNA processing and transcription, nuclear and mitochondrial RNA splicing, RNA editing, ribosomal biogenesis, nuclear cytosolic RNA export, degradation of nonsense RNA and RNA translation. Hence, RNA helicases affect many biological phenomena including cell differentiation, proliferation, development and viral life cycle. Although the RNA helicases are classified into three subgroups, the biological relevance of these groups remains to be defined. In addition, the enzymatic activity of many putative RNA helicases has not been confirmed, this could partly be because of the absence of the appropriate substrate and standard protocol due to the diversity of these enzymes.
Despite the well-conserved attributes of RNA helicases, MDA-5 contains four unique features that could mediate functional divergence. The CARD domain of MDA-5 in its N-terminal region is not found in any previously identified helicases, although the functional significance of this region is currently under investigation. The ATPase A motif of mda-5 is unique and contains LPTGSGKT as opposed to the sequences found in other RNA helicases (GXXGXGKT) and a mutation of the first glycine residue of murine eIF-4A to valine abolishes ATP binding ability. Since leucine is a non-polar amino acid as is valine, but it has a bulkier side chain than valine, MDA-5 may not bind ATP effectively and, hence, may be an ATPase defective helicase or it may require a different energy source and/or metals for activity. This property of MDA-5 may explain the reduction in colony forming efficiency by a expression of a mutant of mda-5 lacking this region of the MDA-5 protein. The HRIGRXXR motif which is critical for RNA binding in vitro is not well conserved in MDA-5 (ARGR1). The functional role of such sequence divergence in the MDA-5 protein remains to be determined. Three yeast hypothetical ORFs share specific features of MDA-5 including ATPase and RNA binding sites, but their biological function has not been ascertained. Complementation assays between these proteins can provide insights on functional and evolutionary relationship among these molecules.
Taken together, the distinctive features of the MDA-5 protein suggest that this molecule represents a member of a new family of RNA helicases. If this is the case, mda-5 may participate in degradation, translation or inhibition of translation of pro- or anti-apoptotic RNA molecules through its RNA helicase domain. Alternatively, mda-5 might be a signal transducer between IFN signals and the apoptotic machinery to prepare the cell for viral invasion and dsRNA accumulation. Localization of GFP-mda-5 fusion protein in the cytoplasm is not contradictory to this hypothesis.
The reporter isolate comprising the mda-5 promoter sequences driving the luciferase cDNA, based on comparison of the quantitation of luciferase assays to fold induction seen in Northern blot analyses of RNA from treated cells, closely mimicked the induction behavior of the endogenous gene. Activation of gene expression occurred primarily with IFN-β and double stranded RNA and to a lesser extent with other IFNS. This DNA sequence is therefore of considerable utility in understanding the regulation of mda-5 in particular and IFN-β inducible genes in general, also encompassing but not restricted to the analysis of compounds including synthetic small molecules that affect this pathway.
Due to the high level of sensitivity, technical simplicity and amenability toward semi-automation of luciferase assays, the mda-5 promoter clone isolates in HO-1 melanoma cells comprise an additional very useful detection and assay system for IFN levels with potentially significant advantages in terms of cost, convenience and reproducibility. Moreover due to the presence of the reporter construct within an in vivo biological context, in addition to the ability to quantitate the amount of exogenously added IFNs or determine responsiveness to specific IFNS, the system is utilizable in the study of compounds of a diverse nature that potentially impinge on the pathway with respect to multiple biological and pharmacological aspects. These include agonistic or antagonistic effects of a specific compound on the IFN pathway combined with the general biological toxicity of that or a combination of compounds, potentially within the same assay itself. The promoter sequence may also be introduced into appropriate cells with an IFN relevant responsiveness similar to that achieved for HO-1 and studied parallel to those described in the HO-1 human melanoma system be performed.
In summary, mda-5 is a new IFN-γ inducible putative RNA helicase containing a CARD motif. The expression of mda-5 is also induced by growth inhibitory and apoptotic signal molecules such as TNF-_and poly IC. Although it was not demonstrated in the present experiments, the ability of IFN-β and poly IC to induce mda-5 expression support the potential for viral induction of this gene. Ectopic expression of mda-5 significantly reduces colony-forming efficiency of HO-1 melanoma cells as expected from the inductive nature and sequence of this gene. The enzymatic activity of MDA-5 remains to be determined. As mentioned earlier, mda-5 may be a defective RNA helicase and a naturally occurring inhibitor of additional unknown helicases. If this is the case, it will be important to identify counterparts of mda-5 which display antiviral, proliferation inhibitory and/or apoptotic roles in cellular physiology. Of particular note is that viruses like hepatitis C virus (HCV) contain a helicase in their genome. Defining the enzymatic activity of MDA-5 may be achieved by modulating the experimental conditions, i.e., by changing reaction conditions including NTP and metal requirements, using potential stimulators like 2′-5′ oligoadenylate, etc. Investigation of the physiological role and molecular basis of mda-5 action should provide important insights into the mechanism of cellular defense conferred by IFN against viral attack. This information should prove valuable in developing new strategies for inhibiting viral pathogenicity and for designing more effective antiviral therapeutics.
Example 2 Reporter Cell LinesReporter cell lines derived from the HO-1 human melanoma cell line containing genomically integrated copies of te Melanoma Differentiaion Associated Gene-5 (Mda-5) upstream promoter sequences.
A Bacterial Artificial Chromosome (BAC), human genomic library was screened to isolate sequenes containing the Mda-5 gene. Two BAC clones containing the coding and upstream sequences of te gene were isolated and characterized.
The complete intron/exon structure of the coding sequences has been determined. An approximately 6 kb fragment upstream of the transcription start site was also isolated. T is fragment was cloned into a promoterless luciferase vector (pGL3 Basic, Promega) and assayed by transient transfection assays for transcriptional activity. The activity displayed by this promoter construct was identical to that of the endogenous gene in terms of responsiveness to inducers (recombinant human β-interferon or synthetic double stranded RNA, poly IC) and time kinetics of induction.
Several sublines containing stably integrated copies of the transcriptionally active luciferase plasmid in a HO-1 human melanoma background was constructed. Independent clonally isolated colonies were expanded and assayed for luciferase activity in the presence of recombinant human β-interferon or synthetic double stranded RNA, poly IC. These clones exhibited luciferase activity similar to the endogenous gene except that the level of induction varied from 10 to 100 fold, probably dependent on the number of integrated copies for each clone (the endogenous gene is induced about 10 fold). While these clones are most responsive to recombinant human β-interferon or synthetic double stranded RNA, poly IC they are also induced at lower levels by other interferons.
These cell lines may be used for:
A. Quantitation of biologically active amounts of interferon produced by various procedures;
B. In rapid high throughput screens to determine or distinguish the relative efficacy of compounds agonistic or antagonistic to the interferon biochemical and signalling pathway;
C. In a rapid high throughput screen to detect small molecules of potential pharmacological and therapeutic utility that synergizes or boosts cellular interferon pathways.
Example 3 Full Length Human Mda-5 Promoter
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- 4. Waxman, S., G. B. Rossi, and T. F., The Status of Differentiation Therapy of Cancer, in The Status of Differentiation Therapy of Cancer, S. Waxman, G. B. Rossi, and T. F., Editors. 1988, Raven Press: New York, N.Y. P. 1-422.
- 5. Fisher, P. B., et al., Effects of combined treatment with interferon and mezerein on melanogenesis and growth in human melanoma cells. Journal of Interferon Research, 1985. 5(1): p. 11-22.
- 6. Jiang, H., et al., Gene Expression Changes Associated with Reversible Growth Suppression and the Induction of Terminal Differentiation in Human Melanoma Cells. Molecular Cellular Differentiation, 1993. 1(1): p. 41-66.
- 7. Jiang, H., S. Waxman, and P. B. Fisher, Regulatin of c-fos, c-jun and jun-B Gene Expression in Human Melanoma Cells Induced to Terminally Differentiate. Molecular cellular Differentiation, 1993. 1(2): p. 197-214.
- 8. Jiang, H. and P. B. Fisher, Use a Sensitive and Efficient Subtraction Hybridization Protocol for the Identification of Genes Differentially Regulated during the Induction of Differentiation, in Human Melanoma Cells. Molecular Cellular Differentiation, 1993. 1(3): p. 285-299.
- 9. Jiang, H., et al., Subtraction hybridization identifies a novel melanoma differentiation associated gene, mda-7, modulated during human melanoma differentiation, growth and progression. Oncogene, 1995. 11(12): p. 2477-86.
- 10. Jiang, H., et al., The melanoma differentiation-associated gene mda-6, which encodes the cyclin-dependent kinase inhibitor p21, is differentially expressed during growth, differentiation and progression in human melanoma cells. Oncogene, 1995. 10(9): p. 1855-64.
- 11. Jiang, H., et al., The melanoma differentiation associated gene mda-7 suppresses cancer cell growth. Proceedings of the National Academy of Sciences of the United States of America, 1996. 93(17): p. 9160-5.
- 12. Lin, J. J., H. Jiang, and P. B. Fisher, Melanoma differentiation associated gene-9, mda-9, is a human gamma interferon responsive gene. Gene, 1998. 207(2): P.105-10.
- 13. Huang, F., et al., Differentiation induction subtraction hybridization (DISH): a strategy for cloning genes displaying differential expression during growth arrest and terminal differentiation. Gene, 1999. 236(1): p. 125-31.
- 14. Huang, F., et al., Identification and temporal expression pattern of genes modulated during irreversible growth arrest and terminal differentiation in human melanoma cells. Oncogene, 1999. 18(23): p. 3546-52.
- 15. Jiang, H., et al., The Melanoma Differentiation Associated Gene-6 (mda-6), Which Encodes the Cyclin-Dependent Kinase Inhibitor p21, May Function as a Negative Regulator of Human Melanoma Growth and Progression. Molecular Cellular Differentiation, 1996. 4(1): p. 67-89.
- 16. Kang, D.-C. And P. B. Fisher, C-ORF, A simple and Efficient Way to Clone Full Open Reading Frame. (Manuscript in preparation). 2000.
- 17. Su, Z.-z., Y. Shi, and P. B. Fisher, Subtraction hybridization identifies a transformation progression-associated gene PEG-3 with sequence homology to a growth arrest and DNA damage-inducible gene. Proc. Natl. Acad. Sci. USA, 1997. 94: p. 9125-30.
- 18. Sambrook, J., E. Fritsch, and T. Maniatis, Molecular Cloning. 2 ed. 1989, New York, N.Y.: Cold Spring Harbor Laboratory Press.
- 19. Hofmann, K., P. Bucher, and J. Tschopp, The CARD domain: a new apoptotic signalling motif. Trends Biochem Sci, 1997. 22(5): p. 155-6.
- 20. Luking, A., U. Stahl, and U. Schmidt, The protein family of RNA Helicases. Crit. Rev Biochem Mol Biol, 1998. 33(4): p. 259-96.
- 21. Rani, M. R. S., et al., Characterization of beta-R1, a gene that is selectively induced by interferon beta (IFN-beta) compared with IFN-alpha. J Biol Chem, 1996. 271(37): p. 22878-84.
Claims
1-35. (canceled)
36. A melanoma differentiation associated gene-5 protein having SEQ ID NO:2.
37. A cell containing a nucleic acid sequence comprising a MDA-5 promoter linked to a heterologous reporter gene.
38. A method for identifying compounds that effect regulation of MDA-5 expression, comprising testing for the ability of a compound to activate reporter gene expression in a reporter cell containing a nucleic acid sequence comprising a MDA-5 promoter linked to a heterologous reporter gene, wherein an increased level of expression of reporter gene indicates that the compound is an interferon agonist.
Type: Application
Filed: May 22, 2007
Publication Date: Nov 8, 2007
Inventors: Paul Fisher (Scarsdale, NY), Dong-Chul Kang (Rutherford, NJ), Rahul Gopalkrishnan (New York, NY)
Application Number: 11/805,429
International Classification: C07K 14/00 (20060101); C12N 5/02 (20060101); C12Q 1/68 (20060101);