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辣椒疫霉作用下叶绿素a/b结合蛋白的表达
引用本文:林明,;贺俐,;徐波,;官德义,;牟少亮,;何水林. 辣椒疫霉作用下叶绿素a/b结合蛋白的表达[J]. 甘蔗(福建), 2008, 0(4): 297-301
作者姓名:林明,  贺俐,  徐波,  官德义,  牟少亮,  何水林
作者单位:[1]福建农林大学生命科学学院,福建福州350002; [2]福建农林大学作物科学学院,福建福州350002; [3]井冈山大学生命科学学院,江西吉安343009
基金项目:国家自然科学基金资助项目(30571128).
摘    要:从基于cDNA-AFLP分析的辣椒应答疫霉侵染的表达谱中找到1个特异表达基因的序列;利用这个序列设计引物,采用基于PCR技术的96孔文库筛选方法,从疫霉处理的辣椒cDNA文库中筛选出这个应答辣椒疫霉侵染的候选基因的全长cDNA;经生物信息学分析,推测这个长度为1022 bp的候选基因为辣椒叶绿素a/b结合蛋白(chlorophyll a/b binding protein,cab)基因;并利用荧光定量PCR法检测cab在疫霉侵染下的表达情况。

关 键 词:辣椒  辣椒疫霉  CDNA-AFLP  叶绿素a/b结合蛋白  实时荧光定量PCR

Expression of the chlorophyll a/b binding protein infected by Phytophthora capsici in pepper
Affiliation:LIN Ming , HE Li, XU Bo , GUAN De-yi, MOU Shao-liang , HE Shui-lin ( 1. College of Life Science ; 2. College of Crop Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian 350002, China; 3. College of Life Science, Jinggangshan University, Ji'an, Jiangxi 343009, China)
Abstract:A sequence of specific expression gene was found in the expression profile responding to infected Phytophthora capsici in popper based on eDNA-FALP analysis, and the sequence was used to design the primer, one positive candidate resistant gene eDNA was isolated from the pepper eDNA library by PCR-based 96-hole screening. According to the results of bioinformafies analysis, it was estimated that the candidate resistant gene with the length of 1022 bp was chlorophyll a/b binding protein gene.
Keywords:pepper  Phytophthora capsici  cDNA-AFLP  chlorophyll a/b binding protein  real time RT-PCR
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