首页 | 本学科首页   官方微博 | 高级检索  
     检索      

小麦-黑麦1BL/1RS易位系99/2439中蛋白激酶基因的克隆
引用本文:王祖华,牛吉山.小麦-黑麦1BL/1RS易位系99/2439中蛋白激酶基因的克隆[J].安徽农业科学,2008,36(14):5823-5825.
作者姓名:王祖华  牛吉山
作者单位:洛阳理工学院环境与化学系,河南洛阳,471023;河南农业大学国家小麦工程技术研究中心,河南郑州,450002
基金项目:河南省杰出青年科学基金资助(021000800).
摘    要:目的]克隆和分析小麦受体蛋白激酶基因片段。方法]对经白粉菌诱导24 h的小麦-黑麦1BL/1RS易位系99/2439叶片中cDNA进行5′-RACE,获得小麦受体蛋白激酶基因的部分片段,并分析其蛋白质序列同源性。结果]通过RACE获得了长度为1 708bp的小麦受体蛋白激酶基因片段。该片段的氨基酸序列(S1125)与基因Lrk19在641个氨基酸跨度内有86%相同,91%相似。S1125与小麦抗锈病基因Lrk10在636个氨基酸跨度内有84%相同,88%相似。S1125可能为丝氨酸-苏氨酸激酶。结论]所克隆的小麦蛋白激酶基因片段与Lrk19基因和小麦抗锈病基因Lrk10具有较高的同源性。

关 键 词:小麦-黑麦1BL/1RS易位系99/2439  RACE  克隆  白粉病
文章编号:0517-6611(2008)14-05823-03
修稿时间:2008年3月10日

Cloning of Protein Kinase Gene in Wheat-rye 1BL/1RS Translocation Line 99/2439
WANG Zu-hua.Cloning of Protein Kinase Gene in Wheat-rye 1BL/1RS Translocation Line 99/2439[J].Journal of Anhui Agricultural Sciences,2008,36(14):5823-5825.
Authors:WANG Zu-hua
Abstract:Objective] The research aimed to clone and analyze the fragment of protein kinase gene in wheat receptor.Method] 5′-RACE wasmade on cDNAin the leaves ofwheat-rye 1BL/1RStranslocation line 99/2439 after beinginduced bypowderymildewfor 24 h toobtain some partofprotein kinase gene in wheat receptor.And the homologyofits protein sequence was analyzed.Result]Through RACE,the fragment of proteinkinase gene in wheat receptor with the length of1 708 bp was obtained.The aminoacid sequence(S1125)ofthis fragment had 86% homologyand91% similarity with gene Lrk19 in the span of 641 amino acids.S1125 had 84% homology and 88% similarity with rust resistance gene Lrk10 inthe span of 636 amino acids.S1125 was probably serine- threonine protein kinase.Conclusion] The cloned fragment of protein kinase gene inwheat receptor had higher homologywith Gene Lrk19 and rust resistance gene Lrk10 in wheat.
Keywords:Wheat-rye 1BL/1RStranslocation line 22/2439  RACE  Cloning  Powderymildew
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号