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Two Novel Y-Type High Molecular Weight Glutenin Genes in Chinese Wheat Landraces of the Yangtze-River Region

机译:江河地区中国小麦地方品种中两个新的Y型高分子量谷蛋白基因

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摘要

High molecular weight glutenin subunits (HMW-GSs) are key determinants for the end-use quality of wheat. Chinese wheat landraces are an important resource for exploring novel HMW-GS genes to improve the wheat baking quality. Two novel Glu-1Dy HMW-GSs (designated as 1Dy12.6 and 1Dy12.7) were identified and cloned from two Chinese wheat landraces Huazhong830 and Luosimai. The 1Dy12.6 and 1Dy12.7 subunits were deposited as the NCBInr Acc. No , and , respectively. The full open reading frames (ORFs) of 1Dy12.6 and 1Dy12.7 were 2022 bp and 1977 bp, encoding for proteins of 673 and 658 amino acid residues, respectively. Each contains four typical primary regions of HMW-GSs (a signal peptide, N- and C-terminal regions, and a central repetitive region). Their deduced molecular masses (70,165 Da and 68,400 Da) were strikingly consistent with those identified by MALDI-TOF-MS (69,985Da and 68,407 Da). The 1Dy12.6 is the largest 1Dy glutenin subunits cloned in common wheat up to date, containing longer repetitive central domains than other 1Dy encoded proteins. In comparison with the most similar active 1Dy alleles previously reported, the newly discovered alleles contained a total of 20 SNPs and 3 indels. The secondary structure prediction indicated that 1Dy12.6 and 1Dy12.7 have similar proportion of α-helix, β-turn, and β-bend to those of 1Dy10 (). The phylogenetic analysis illustrated that the x- and y-type subunits of glutenins were well separated, but both 1Dy12.6 and 1Dy12.7 were clustered with the other Glu-1Dy alleles. Our results revealed that the 1Dy12.6 and 1Dy12.7 subunit have potential to strengthen gluten polymer interactions, and are valuable genetic resources for wheat quality improvement.
机译:高分子量谷蛋白亚基(HMW-GSs)是决定小麦最终用途质量的关键因素。中国小麦地方品种是探索新型HMW-GS基因以提高小麦烘烤品质的重要资源。鉴定了两个新颖的Glu-1Dy HMW-GS(分别命名为1Dy12.6和1Dy12.7),并从两个中国小麦地方品种华中830和洛斯麦进行了克隆。 1Dy12.6和1Dy12.7亚基作为NCBInr Acc存放。否,和。 1Dy12.6和1Dy12.7的全开放阅读框(ORF)为2022 bp和1977 bp,分别编码673和658个氨基酸残基的蛋白质。每个都包含HMW-GS的四个典型主要区域(信号肽,N和C末端区域以及中央重复区域)。他们推导的分子量(70,165 Da和68,400 Da)与MALDI-TOF-MS鉴定的分子量(69,985Da和68,407 Da)非常一致。 1Dy12.6是迄今为止在普通小麦中克隆的最大的1Dy谷蛋白亚基,比其他1Dy编码的蛋白质包含更长的重复中央结构域。与先前报道的最相似的活跃1Dy等位基因相比,新发现的等位基因总共包含20个SNP和3个indel。二级结构预测表明1Dy12.6和1Dy12.7具有与1Dy10()相似的α-螺旋,β-turn和β-bend比例。系统发育分析表明,谷蛋白的x型和y型亚基被很好地分离,但是1Dy12.6和1Dy12.7都与其他Glu-1Dy等位基因聚在一起。我们的结果表明,1Dy12.6和1Dy12.7亚基具有增强面筋聚合物相互作用的潜力,并且是改善小麦品质的宝贵遗传资源。

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