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New Insights into the Organization, Recombination, Expression and Functional Mechanism of Low Molecular Weight Glutenin Subunit Genes in Bread Wheat

机译:面包小麦低分子量谷蛋白亚基基因的组织,重组,表达及功能机理的新见解

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摘要

The bread-making quality of wheat is strongly influenced by multiple low molecular weight glutenin subunit (LMW-GS) proteins expressed in the seeds. However, the organization, recombination and expression of LMW-GS genes and their functional mechanism in bread-making are not well understood. Here we report a systematic molecular analysis of LMW-GS genes located at the orthologous Glu-3 loci (Glu-A3, B3 and D3) of bread wheat using complementary approaches (genome wide characterization of gene members, expression profiling, proteomic analysis). Fourteen unique LMW-GS genes were identified for Xiaoyan 54 (with superior bread-making quality). Molecular mapping and recombination analyses revealed that the three Glu-3 loci of Xiaoyan 54 harbored dissimilar numbers of LMW-GS genes and covered different genetic distances. The number of expressed LMW-GS in the seeds was higher in Xiaoyan 54 than in Jing 411 (with relatively poor bread-making quality). This correlated with the finding of higher numbers of active LMW-GS genes at the A3 and D3 loci in Xiaoyan 54. Association analysis using recombinant inbred lines suggested that positive interactions, conferred by genetic combinations of the Glu-3 locus alleles with more numerous active LMW-GS genes, were generally important for the recombinant progenies to attain high Zeleny sedimentation value (ZSV), an important indicator of bread-making quality. A higher number of active LMW-GS genes tended to lead to a more elevated ZSV, although this tendency was influenced by genetic background. This work provides substantial new insights into the genomic organization and expression of LMW-GS genes, and molecular genetic evidence suggesting that these genes contribute quantitatively to bread-making quality in hexaploid wheat. Our analysis also indicates that selection for high numbers of active LMW-GS genes can be used for improvement of bread-making quality in wheat breeding.
机译:种子中表达的多种低分子量谷蛋白亚基(LMW-GS)蛋白强烈影响小麦的面包制作质量。然而,LMW-GS基因的组织,重组和表达及其在面包制作中的功能机制尚不十分清楚。在这里,我们报告了使用互补方法(全基因组范围内的基因成员表征,表达谱,蛋白质组学分析)对位于面包小麦直向同源Glu-3位点(Glu-A3,B3和D3)的LMW-GS基因进行的系统分子分析。鉴定出用于小烟54的14个独特的LMW-GS基因(具有卓越的制面包质量)。分子作图和重组分析表明,小盐54号的三个Glu-3基因座具有不同数量的LMW-GS基因,并且覆盖了不同的遗传距离。小yan 54种子中表达的LMW-GS数量高于京411(制面包质量较差)。这与在小岩54的A3和D3基因座上发现更多的活跃LMW-GS基因相关。使用重组自交系的关联分析表明,由Glu-3基因座等位基因的遗传组合产生的正向相互作用具有更多的活性。 LMW-GS基因通常对于重组子代获得很高的Zeleny沉降值(ZSV)至关重要,Zeleny沉降值是面包制作质量的重要指标。较高数量的活性LMW-GS基因倾向于导致ZSV升高,尽管这种趋势受遗传背景的影响。这项工作为LMW-GS基因的基因组组织和表达提供了重要的新见识,分子遗传证据表明这些基因在数量上有助于六倍体小麦的面包制作质量。我们的分析还表明,选择大量活跃的LMW-GS基因可用于改善小麦育种中的面包制作质量。

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