中国农业科学 ›› 2006, Vol. 39 ›› Issue (9): 1743-1750 .

• 作物遗传育种·种质资源 • 上一篇    下一篇

四川小麦地方品种AS1643中α/β醇溶蛋白基因

陈华萍   

  1. 四川农业大学生命科学与理学院
  • 收稿日期:2005-08-29 修回日期:2005-12-16 出版日期:2006-09-10 发布日期:2006-09-10
  • 通讯作者: 陈华萍

Sequence analysis of α/β-gliadin genesfrom Sichuanwheat landrace AS1643

  1. 四川农业大学生命科学与理学院
  • Received:2005-08-29 Revised:2005-12-16 Online:2006-09-10 Published:2006-09-10

摘要: 用PCR方法从四川小麦地方品种AS1643中克隆到3个α/β-醇溶蛋白基因,即Gli-AS1643-1(GenBank No.DQ166376)、Gli-AS1643-2(GenBank No.DQ166377)和Gli-AS1643-3(GenBank No.DQ166378)。其中,Gli-AS1643-1和Gli-AS1643-2的编码区长度分别为873bp和852bp,可编码270和263个氨基酸残基的成熟蛋白。Gli-AS1643-3由于在编码区内有一个提前终止密码子,为不可编码成熟蛋白的假基因。序列比较显示Gli-AS1643-1、Gli-AS1643-2和 Gli-AS1643-3分别与GenBank中的α/β-醇溶蛋白基因具有较高的一致性,且序列结构非常相似。它们的N-端氨基酸序列与各种α-、β-、γ-和α/β-醇溶蛋白的基本一致,但与ω-醇溶蛋白和低分子量谷蛋白亚基的明显不同。N-端12肽串联重复紧密相关的5个脯氨酸框和类似于微卫星序列编码的2个多聚谷氨酰胺区域。在Gli-AS1643-2的N-端存在腹泻疾病活性序列,C-端含有12型腺病毒感染序列。Gli-AS1643-1、Gli-AS1643-2和Gli-AS1643-3各由6个保守的半胱氨酸残基形成3个分子内二硫键。

关键词: 小麦, α/β-醇溶蛋白基因, 序列分析

Abstract: Using PCR amplification method, the full coding regions (open reading frame, ORF) of three α/β-gliadin genes Gli-AS1643-1 (GenBank No.DQ166376), Gli-AS1643-2 (GenBank No.DQ166377) and Gli-AS1643-3 (GenBank No.DQ166378), were isolated form the genomic DNA of Sichuan wheat landrace AS1643. Among which, Gli-AS1643-1 and Gli-AS1643-2 were 873 bp and 852 bp, and could encode two mature proteins with 270 and 263 amino acid residues, respectively. Due to one stop codon in its coding region, Gli-AS1643-3 was a pseudogene. Multiple sequence alignment analysis suggested that Gli-AS1643-1, Gli-AS1643-2 and Gli-AS1643-3 have the higher similarity in their structure with the known α/β-gliadin genes in GenBank. N-terminal amino acid sequences of the three cloned genes were basically consistent with other α-, β-, γ- and α/β-gliadins, whereas it was clearly different with ω-gliadins and LMW-GS. N-terminal amino acid sequence was dodecapeptide tandem repeat with five more closely proline boxes and two polyglutamine domains encoded by microsatellite-like sequences. Sequence active in celiac disease and adenovirus type twelve infection sequences were presented in N-domain and in C-domain of Gli-AS1643-2, respectively. The six conserved cysteine residues would form three intramolecular disulfide bonds in Gli-AS1643-1, Gli-AS1643-2 and Gli-AS1643-3, respectively.

Key words: Wheat, α/β-gliadin gene, Sequence analysis