Abstract: Disclosed are methods of producing plants with an improved regeneration efficiency using Growth-Regulating Factor (GRF), GRF-Interacting Factor (GIF), or chimeric GRF-GIF genes and proteins. The disclosure also provides plants with an improved regeneration efficiency that are produced by the disclosed methods, methods of reducing the use of exogenous cytokinins in the regeneration of plants, and methods of improving the regeneration efficiency of plants.

Abstract: The invention provides a wheat cell, part, tissue culture or whole plant comprising at least one disrupted KRP gene of the present invention. The present invention also provides methods of increasing weight, size, and/or number of one or more organs, and/or yield of a wheat plant by utilizing the disrupted KRP genes of the present invention. Furthermore, methods of breeding wheat plants to produce new wheat plants having increased weight, size, and/or number of one or more organs, and/or yield are provided. The present invention provides isolated Kinase Inhibitor Protein (KIP) Related Protein (KRP) polynucleotide sequences and isolated KRP polypeptide sequences and methods of their use.

Abstract: An isolated nucleic acid molecule comprising a nucleotide sequence which encodes a polypeptide comprising both a steroidogenic acute regulatory protein-related lipid transfer (START) domain and a kinase domain is provided, as well as plant cells and transgenic plants comprising said nucleic acid molecule, said transgenic plants being resistant to plant diseases.

Abstract: The invention provides a wheat cell, part, tissue culture or whole plant comprising at least one disrupted KRP gene of the present invention. The present invention also provides methods of increasing weight, size, and/or number of one or more organs, and/or yield of a wheat plant by utilizing the disrupted KRP genes of the present invention. Furthermore, methods of breeding wheat plants to produce new wheat plants having increased weight, size, and/or number of one or more organs, and/or yield are provided. The present invention provides isolated Kinase Inhibitor Protein (KIP) Related Protein (KRP) polynucleotide sequences and isolated KRP polypeptide sequences and methods of their use.

Abstract: The invention provides a wheat cell, part, tissue culture or whole plant comprising at least one disrupted KRP gene of the present invention. The present invention also provides methods of increasing weight, size, and/or number of one or more organs, and/or yield of a wheat plant by utilizing the disrupted KRP genes of the present invention. Furthermore, methods of breeding wheat plants to produce new wheat plants having increased weight, size, and/or number of one or more organs, and/or yield are provided. The present invention provides isolated Kinase Inhibitor Protein (KIP) Related Protein (KRP) polynucleotide sequences and isolated KRP polypeptide sequences and methods of their use.

Abstract: The invention provides a wheat cell, part, tissue culture or whole plant comprising at least one disrupted KRP gene of the present invention. The present invention also provides methods of increasing weight, size, and/or number of one or more organs, and/or yield of a wheat plant by utilizing the disrupted KRP genes of the present invention. Furthermore, methods of breeding wheat plants to produce new wheat plants having increased weight, size, and/or number of one or more organs, and/or yield are provided. The present invention provides isolated Kinase Inhibitor Protein (KIP) Related Protein (KRP) polynucleotide sequences and isolated KRP polypeptide sequences and methods of their use.

Abstract: An isolated nucleic acid molecule comprising a nucleotide sequence which encodes a polypeptide comprising both a steroidogenic acute regulatory protein-related lipid transfer (START) domain and a kinase domain is provided, as well as plant cells and transgenic plants comprising said nucleic acid molecule, said transgenic plants being resistant to plant disease.

Abstract: The present invention provides wheat NAC nucleic acids and proteins that modulate grain protein content and senescence in plants. Overexpression of a NAC coding sequence can accelerate senescence and increase grain protein content and inhibition of expression can delay senescence. The invention also provides methods of using the nucleic acids to produce transgenic plants with altered grain protein content or senescence.

Abstract: The present invention NAC nucleic acids and proteins that modulate grain protein content and senescence in plants. The invention also provides methods of using the nucleic acids to produce transgenic plants with altered grain protein content or senescence.

Abstract: Winter wheats require several weeks at low temperature to flower. This process called vernalization is controlled mainly by a pair of genes, VRN1 and VRN2. The present invention includes the sequences of the VRN1 and VRN2 genes, proteins and promoter regions, transgenic plants containing the genes and/or promoters and uses of the foregoing. Of particular interest are temperate cereals with modified vernalization responses or flowering times.

Abstract: Winter wheats require several weeks at low temperature to flower. This process called vernalization is controlled mainly by the VRN1 gene. Using 6,190 gametes VRN1 was found to be completely linked to MADS-box genes AP1 and AGLG1 in a 0.03-cM interval flanked by genes Cysteine and Cytochrome B5. No additional genes were found between the last two genes in 324-kb of wheat sequence or in the colinear regions in rice and sorghum. Wheat AP1 and AGLG1 genes were similar to Arabidopsis meristem identity genes AP1 and AGL2 respectively. AP1 transcription was regulated by vernalization in both apices and leaves, and the progressive increase of AP1 transcription was consistent with the progressive effect of vernalization on flowering time. Vernalization was required for AP1 transcription in apices and leaves in winter wheat but not in spring wheat. AGLG1 transcripts were detected during spike differentiation but not in vernalized apices or leaves, suggesting that AP1 acts upstream of AGLG1.

Abstract: Winter wheats require several weeks at low temperature to flower. This process called vernalization is controlled mainly by a pair of genes, VRN1 and VRN2. The present invention includes the sequences of the VRN1 and VRN2 genes, proteins and promoter regions, transgenic plants containing the genes and/or promoters and uses of the foregoing. Of particular interest are temperate cereals with modified vernalization responses or flowering times.