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小麦—簇毛麦6VS/6AL易位系叶片cDNA文库构建及鉴定
引用本文:牛吉山,于玲,陈佩度,刘大钧.小麦—簇毛麦6VS/6AL易位系叶片cDNA文库构建及鉴定[J].南京农业大学学报,2001,24(1):5-8.
作者姓名:牛吉山  于玲  陈佩度  刘大钧
作者单位:南京农业大学农业部
基金项目:86 3计划资助项目! (Z 17 0 4 0 1)
摘    要:用表达型质粒载体p^SPORT1构建了经白粉菌(Erysiphe graminis)诱导48h和未经诱导的小麦-簇毛麦6VS/6AL易位系(Triticum aestivum-Haynaldia villosa translocation lin)叶片cDNA库各一个,库宿主菌为E.coli DH10B,非诱导库包含约50万个重组cDNA克隆,平均插入征段为1.25kb,主要分布在400bp-2.2kb。诱导民含约30万个重组cDNA克隆,平均插入片段1.2kb。用克隆的病程相关基因(pathogenesis related gene),=-小麦类甜蛋白基因pWIR作探针,进行杂交筛库,杂交信号明显,重复性好。

关 键 词:小麦-簇毛麦6VS/6AL易位系  cDNA文库  白粉病  基因克隆  抗病基因  鉴定
文章编号:1000-2030(2001)01-0005-04
修稿时间:2000年9月6日

cDNA library construction and identification of Triticum aestivum Haynaldia villosa 6VS/6AL translocation line
Niu Jishan,Yu Lin,Chen Peidu,Liu Dajun.cDNA library construction and identification of Triticum aestivum Haynaldia villosa 6VS/6AL translocation line[J].Journal of Nanjing Agricultural University,2001,24(1):5-8.
Authors:Niu Jishan  Yu Lin  Chen Peidu  Liu Dajun
Institution:Niu Jishan,Yu Ling,Chen Peidu * and Liu Dajun
Abstract:Two cDNA libraries of Triticum aestivum-Haynald ia villosa 6VS/6AL translocation line were constructed using mRNA from leaves of its plants induced and non-induced with Erysiphe graminis.An expression pla smid pSPORT 1 introduced into E.coli DH10B was used as cloning vector. The cDNA library of pathogen induced translocation line comprised of about 300 0 00 recombinant cDNA clones with average insert size of 1.2 kb,and that of non -induced translocation line consisted of aproximately 500 000 recombinant cDNA clones with average insert size of 1.25 kb,ranging ba sically from 0.4 to 2.2 kb.The library was successfully screened with a wheat thaumatin-like protein gene pWIR as the probe.
Keywords:VS/6AL translocation line  cDNA library  Erysiphe graminis  induce
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