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智利大麦的D型醇溶蛋白:小麦改良的新变异来源。

D hordeins of Hordeum chilense: a novel source of variation for improvement of wheat.

作者信息

Pistón Fernando, Shewry Peter R, Barro Francisco

机构信息

Instituto de Agricultura Sostenible, CSIC, Apdo. 4084, 14080 Córdoba, Spain.

出版信息

Theor Appl Genet. 2007 Jun;115(1):77-86. doi: 10.1007/s00122-007-0542-0. Epub 2007 Apr 26.

Abstract

The high molecular weight subunits of wheat (Triticum aestivum L.) glutenin (HMW-GS) are important in determining the bread-making quality of flour and dough. There is therefore interest in transferring orthologous HMW-GS present in other grass species into wheat by wide crossing in order to extend the range of end use properties. In this work, we have isolated and characterized two genes encoding D hordeins from Hordeum chilense (Roem. et Schult.) lines H1 and H7, representing two ecotypes. The fragments were 4,305 bp for line H1 and 4,227 for line H7 and contained the promoter, coding and terminator regions. Both sequences differ in the presence of single base changes (SNPs) and insertions/deletions in the open reading frame (ORF). The encoded proteins comprise 870 and 896 amino acids for lines H1 and H7, respectively. The primary structure is similar to those of D hordeins of cultivated barley (H. vulgare L.) and HMW-GS from wheat. However, the D hordeins from H. chilense are significantly larger than those from cultivated barley due to the presence of longer repetitive regions. The H. chilense D hordeins also differ from those of cultivated barley in the distribution of the cysteine residues: whereas the D hordeins of cultivated barley contain ten cysteines with four in the repetitive domain, only nine are present in the H. chilense proteins with two in the repetitive domain. As in the HMW-GS, the central part of the D hordein proteins comprises repeated sequences based on short peptide motifs. The repetitive domain is divided in three regions named as R1 (N-terminal repeats), R2 (central degenerate repeats) and R3 (C-terminal repeats). Hexapeptide motifs are present throughout the repetitive domains of D hordeins with a consensus motif of PFQGQQ in R1 and R2 and PHQGQQ in R3. In addition, the tetrapeptide motif TTVS, which is characteristic of D hordeins of cultivated barley is present in the repetitive domain close to the protein C-terminus.

摘要

小麦(Triticum aestivum L.)谷蛋白的高分子量亚基(HMW-GS)对于决定面粉和面团的烘焙品质至关重要。因此,人们有兴趣通过远缘杂交将其他禾本科物种中存在的直系同源HMW-GS导入小麦,以扩展其最终使用特性的范围。在这项研究中,我们从代表两种生态型的智利大麦(Hordeum chilense (Roem. et Schult.))品系H1和H7中分离并鉴定了两个编码D醇溶蛋白的基因。H1品系的片段为4305 bp,H7品系的片段为4227 bp,包含启动子、编码区和终止区。两个序列在开放阅读框(ORF)中存在单碱基变化(SNP)和插入/缺失。H1和H7品系编码的蛋白质分别包含870和896个氨基酸。其一级结构与栽培大麦(H. vulgare L.)的D醇溶蛋白和小麦的HMW-GS相似。然而,由于存在更长的重复区域,智利大麦的D醇溶蛋白比栽培大麦的显著更大。智利大麦的D醇溶蛋白在半胱氨酸残基的分布上也与栽培大麦不同:栽培大麦的D醇溶蛋白含有10个半胱氨酸,其中4个在重复结构域,而智利大麦的蛋白质中只有9个半胱氨酸,其中2个在重复结构域。与HMW-GS一样,D醇溶蛋白的中心部分由基于短肽基序的重复序列组成。重复结构域分为三个区域,命名为R1(N端重复)、R2(中心简并重复)和R3(C端重复)。六肽基序存在于D醇溶蛋白的整个重复结构域中,R1和R2中的共有基序为PFQGQQ,R3中的为PHQGQQ。此外,栽培大麦D醇溶蛋白特有的四肽基序TTVS存在于靠近蛋白质C端的重复结构域中。

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