首页> 美国卫生研究院文献>Genetics >Novel x-Type High-Molecular-Weight Glutenin Genes From Aegilops tauschii and Their Implications on the Wheat Origin and Evolution Mechanism of Glu-D1-1 Proteins
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Novel x-Type High-Molecular-Weight Glutenin Genes From Aegilops tauschii and Their Implications on the Wheat Origin and Evolution Mechanism of Glu-D1-1 Proteins

机译:taegchii的新型x型高分子量谷蛋白基因及其对小麦起源和Glu-D1-1蛋白进化机制的影响

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摘要

Two new x-type high-molecular-weight glutenin subunits with similar size to 1Dx5, designated 1Dx5*t and 1Dx5.1*t in Aegilops tauschii, were identified by SDS–PAGE, RP-HPLC, and MALDI-TOF-MS. The coding sequences were isolated by AS-PCR and the complete ORFs were obtained. Allele 1Dx5*t consists of 2481 bp encoding a mature protein of 827 residues with deduced Mr of 85,782 Da whereas 1Dx5.1*t comprises 2526 bp encoding 842 residues with Mr of 87,663 Da. The deduced Mr's of both genes were consistent with those determined by MALDI-TOF-MS. Molecular structure analysis showed that the repeat motifs of 1Dx5*t were correspondingly closer to the consensus compared to 1Dx5.1*t and 1Dx5 subunits. A total of 11 SNPs (3 in 1Dx5*t and 8 in 1Dx5.1*t) and two indels in 1Dx5*t were identified, among which 8 SNPs were due to C-T or A-G transitions (an average of 73%). Expression of the cloned ORFs and N-terminal sequencing confirmed the authenticities of the two genes. Interestingly, several hybrid clones of 1Dx5*t expressed a slightly smaller protein relative to the authentic subunit present in seed proteins; this was confirmed to result from a deletion of 180 bp through illegitimate recombination as well as an in-frame stop codon. Network analysis demonstrated that 1Dx5*t, 1Dx2t, 1Dx1.6t, and 1Dx2.2* represent a root within a network and correspond to the common ancestors of the other Glu-D-1-1 alleles in an associated star-like phylogeny, suggesting that there were at least four independent origins of hexaploid wheat. In addition to unequal homologous recombination, duplication and deletion of large fragments occurring in Glu-D-1-1 alleles were attributed to illegitimate recombination.
机译:通过SDS鉴定了两个新的x型高分子量谷蛋白亚基,其大小与1Dx5类似,分别被命名为Aegilops tauschii中的1Dx5 * t 和1Dx5.1 * t 。 -PAGE,RP-HPLC和MALDI-TOF-MS。通过AS-PCR分离编码序列,获得完整的ORF。等位基因1Dx5 * t 由2481 bp的成熟蛋白组成,编码827个残基的成熟蛋白,推导的Mr为85,782 Da,而1Dx5.1 * t 包括2526 bp,编码842个残基,Mr为87,663大两个基因的推导的Mr's与通过MALDI-TOF-MS确定的那些一致。分子结构分析表明,与1Dx5.1 * t 和1Dx5亚基相比,1Dx5 * t 的重复基序相应地更接近共有。总共鉴定出11个SNP(1Dx5 * t 中的3个和1Dx5.1 * t 中的8个)和1Dx5 * t 中的两个indel。 ,其中8个SNP归因于CT或AG转换(平均73%)。克隆的ORF的表达和N端测序证实了这两个基因的真实性。有趣的是,相对于种子蛋白中存在的真实亚基, 1Dx5 * t 的几个杂种克隆表达的蛋白略小。证实这是由于通过非法重组以及框内终止密码子而缺失了180 bp。网络分析表明 1Dx5 * t 1Dx2 t 1Dx1.6 t < / sup> 1Dx2.2 * 表示网络中的根,并与其他 Glu-D-1的共同祖先相对应-1 等位基因在相关的星形系统发育中,提示至少有四个独立的六倍体小麦起源。除了不平等的同源重组外, Glu-D-1-1 等位基因中出现的大片段的重复和缺失也归因于非法重组。

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