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首页> 外文期刊>Plant Physiology >Genetic and Molecular Characterization of the VRN2 Loci in Tetraploid Wheat1,[W],[OA]
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Genetic and Molecular Characterization of the VRN2 Loci in Tetraploid Wheat1,[W],[OA]

机译:四倍体小麦1,[W],[OA]中VRN2基因座的遗传和分子特征

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摘要

Winter wheat (Triticum spp.) varieties require long exposures to low temperatures to flower, a process called vernalization. The VRN2 locus includes two completely linked zinc finger-CCT domain genes (ZCCT1 and ZCCT2) that act as flowering repressors down-regulated during vernalization. Deletions or mutations in these two genes result in the elimination of the vernalization requirement in diploid wheat (Triticum monococcum). However, natural allelic variation in these genes has not been described so far in polyploid wheat (tetraploid Triticum turgidum and hexaploid Triticum aestivum). A tetraploid wheat population segregating for both VRN-A2 and VRN-B2 loci facilitated the characterization of different alleles. Comparisons between functional and nonfunctional alleles revealed that both ZCCT1 and ZCCT2 genes are able to confer vernalization requirement and that different ZCCT genes are functional in different genomes. ZCCT1 and ZCCT2 proteins from nonfunctional vrn2 alleles have mutations at arginine amino acids at position 16, 35, or 39 of the CCT domain. These positions are conserved between CCT and HEME ACTIVATOR PROTEIN2 (HAP2) proteins, supporting a model in which the action of CCT domains is mediated by their interactions with HAP2/HAP3/HAP5 complexes. This study also revealed natural variation in gene copy number, including a duplication of the functional ZCCT-B2 gene and deletions or duplications of the complete VRN-B2 locus. Allelic variation at the VRN-B2 locus was associated with a partially dominant effect, which suggests that variation in the number of functional ZCCT genes can be used to expand allelic diversity for heading time in polyploid wheat and, hopefully, improve its adaptation to different environments.
机译:冬小麦(Triticum spp。)品种需要长时间暴露于低温下才能开花,这一过程称为春化。 VRN2基因座包括两个完全连接的锌指-CCT域基因(ZCCT1和ZCCT2),它们在春化期间充当下调的开花抑制因子。这两个基因的缺失或突变导致二倍体小麦(Triticum monococcum)的春化需求消除。但是,到目前为止,尚未在多倍体小麦(四倍体小麦和六倍体小麦)中描述这些基因的自然等位基因变异。分离为VRN-A2和VRN-B2基因座的四倍体小麦群体有助于表征不同的等位基因。功能性和非功能性等位基因之间的比较表明,ZCCT1和ZCCT2基因均能够满足春化要求,并且不同的ZCCT基因在不同的基因组中具有功能。来自非功能性vrn2等位基因的ZCCT1和ZCCT2蛋白在CCT域的16、35或39位的精氨酸氨基酸处具有突变。这些位置在CCT和HEME激活蛋白2(HAP2)蛋白之间是保守的,支持其中CCT域的作用由其与HAP2 / HAP3 / HAP5复合物的相互作用介导的模型。这项研究还揭示了基因拷贝数的自然变化,包括功能性ZCCT-B2基因的重复和完整VRN-B2基因座的缺失或重复。 VRN-B2基因座的等位基因变异与部分显性效应有关,这表明功能性ZCCT基因数量的变异可用于扩大多倍体小麦抽穗期的等位基因多样性,并有望改善其对不同环境的适应性。

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  • 来源
    《Plant Physiology 》 |2009年第1期| p.245-257| 共13页
  • 作者单位

    Department of Plant Sciences, University of California, Davis, California 95616–8515 (A.D., C.L., J.D.);

    Instituto de Recursos Biológicos, Instituto Nacional de Tecnología Agropecuaria, Buenos Aires, Argentina (G.T.);

    and Department of Plant and Soil Sciences, Oklahoma State University, Stillwater, Oklahoma 74078 (L.Y.);

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