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鉴定和野生二粒小麦高分子量谷蛋白亚基 1By16*的分子特征。

Identification and molecular characterisation of HMW glutenin subunit 1By16* in wild emmer.

机构信息

Key Laboratory of Genetics and Biotechnology, College of Life Science, Capital Normal University, Beijing 100048, China.

出版信息

J Appl Genet. 2012 Aug;53(3):249-58. doi: 10.1007/s13353-012-0101-5. Epub 2012 May 30.

DOI:10.1007/s13353-012-0101-5
PMID:22644727
Abstract

In this study, a novel y-type high molecular weight glutenin subunit (HMW-GS) in wild emmer wheat Triticum turgidum L. var. dicoccoides (Körn.) accession KU1952 was identified by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE), capillary electrophoresis (CE) and matrix-assisted laser desorption ionisation/time-of-flight/mass spectrometry (MALDI-TOF-MS). Its electrophoretic mobility and molecular weight were similar to those of 1By16 and was designated as 1By16*. The complete coding sequence of the 1By16* gene isolated by allelic-specific polymerase chain reaction (AS-PCR) consists of 2,157 bp, encoding 729 amino acid residues. The real presence and authenticity of the 1By16* gene in KU1952 were further confirmed by liquid chromatography-tandem mass spectrometry (LC-MS/MS), heterologous expression and Western blotting. The molecular structure as well as phylogenetic analysis revealed that 1By16* had 21 single-nucleotide polymorphism (SNP) variations and possessed greater similarity with superior quality subunits 1By15 and 1By16 of common wheat. Secondary structure prediction displayed higher α-helix and β-strand contents in the 1By16* subunit, which could form a superior gluten structure and, consequently, might have positive effects on dough quality. Our results suggest that 1By16* is expected to be a new potential gene for wheat quality improvement.

摘要

在这项研究中,通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)、毛细管电泳(CE)和基质辅助激光解吸电离/飞行时间/质谱(MALDI-TOF-MS),鉴定出野生二粒小麦 Triticum turgidum L. var. dicoccoides (Körn.) accession KU1952 中的一种新型 Y 型高分子量麦谷蛋白亚基(HMW-GS)。其电泳迁移率和分子量与 1By16 相似,被命名为 1By16*。通过等位基因特异性聚合酶链反应(AS-PCR)分离的 1By16基因的完整编码序列由 2,157 bp 组成,编码 729 个氨基酸残基。通过液相色谱-串联质谱(LC-MS/MS)、异源表达和 Western blot 进一步证实了 1By16基因在 KU1952 中的真实存在和真实性。分子结构和系统发育分析表明,1By16有 21 个单核苷酸多态性(SNP)变异,与普通小麦的优质亚基 1By15 和 1By16 具有更大的相似性。二级结构预测显示 1By16亚基具有更高的α-螺旋和β-折叠含量,能够形成更好的面筋结构,从而可能对面筋质量产生积极影响。我们的结果表明,1By16*有望成为小麦品质改良的新潜在基因。

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