Use of the AP1 gene promoter to control the vernalization response and flowering time in grasses
OwnerJorge Dubcovsky, Liuling Yaninventors
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OwnerJorge Dubcovsky, Liuling Yaninventors
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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. No differences were detected between genotypes with different VRN1 alleles in the AP1 and AGLG1 coding regions, but three independent deletions were found in the promoter region of AP1. These results suggest that AP1 is a better candidate for VRN1 than AGLG1. The epistatic interactions between vernalization genes VRN1 and VRN2 suggested a model in which VRN2 would repress directly or indirectly the expression of AP1. A mutation in the promoter region of AP1 would result in the lack of recognition of the repressor and in a dominant spring growth habit.
A recombinant AP1 promoter sequence wherein said AP1 promoter sequence hybridizes to the nucleic acid molecule of SEQ ID NO:12 or the complement thereof under high stringency conditions, wherein said high stringency conditions consist of hybridization to filter-bound DNA in 5×SSC, 2% sodium dodecyl sulfate (SDS), 100 ug/ml single stranded DNA at 55-65° C., and washing in 0.1×SSC and 0.1% SDS at 60-65°.
Seed from the transgenic plant of claim 22.
A recombinant AP1 promoter comprising a nucleotide sequence selected from the group consisting of SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12 and SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17 and SEQ ID NO:23.
A molecular marker for Vrn1 derived from a gene selected from the group of genes depicted in FIG. 1.
Dependencies are inferred from the claim text.