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作者	单位
李艳亮1, 高翔1,2, 陈其皎1,2, 董剑1,2, 赵万春1,2, 王明霞1, 李敏1,陈瑞佶1,庞红喜1,2,李哲清1,2,刘俊1,2	1.西北农林科技大学农学院，陕西杨凌 712100； 2.陕西省小麦工程技术研究中心/陕西省小麦新品种培育工程研究中心陕西杨凌 712100

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中文摘要:

为了挖掘和有效利用陕253中的优良基因，根据LMW GS编码基因5′和3′端的保守序列设计引物，采用PCR方法以陕253的基因组DNA为模板进行扩增，分别回收并克隆到载体上，测序后得到11个新LMW GS基因。GenBank登录号分别为GQ892576~GQ892580和GQ892583~GQ892588，其长度为903~1 081 bp。其中，GQ892576、GQ892585、GQ892586、GQ892587和GQ892588具有完整编码区，可分别编码305、351、298、351和307个氨基酸残基的成熟蛋白。而GQ892577、GQ892578、GQ892579、GQ892580、GQ892583和GQ892584由于在编码区内出现提前终止密码子，推测为假基因。推导的氨基酸序列结果显示：它们都具有LMW m型低分子量谷蛋白亚基的典型结构特征。

英文摘要:

In order to find and utilize the advantageous genes of Shaan 253 and provide more important information for the further genetic improvement. The full length coding region (open reading frame, ORF) of low molecular weight glutenin subunit (LMW GS) gene was amplified from cultivar “Shaan253” by using the primer pairs designed according to the conservative sequences of 5'and 3'terminal domains. The amplified DNA fragment was separated and recovered from agarose gel, subsequently cloned into pMD19 T vector, and then transformed into E.coli strain DH5α. eleven positive clones (GenBank accession number. GQ892576 GQ892580, GQ892583 GQ892588) were selected and sequenced. these genes possessed the nucleotide sequences from 903bp to 1 081bp. GQ892576, GQ892585, GQ892586, GQ892587 and GQ892588 had the whole CDS, and encoded a mature protein of 305、351、298、351 and 307 amino acid residues, respectively. GQ892577, GQ892578, GQ892579, GQ892580, GQ892583, GQ892584 were putative pseudogenes due to the presence of inframe stop codons in these coding region. Deduced amino acid sequence showed these sequences were the typical structure features of LMW m type.

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