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茶树花粉特异蛋白基因CsPSP的反义载体构建
引用本文:龚莹,余梅,江昌俊,吴凡,吉虎,徐凯,臧洁.茶树花粉特异蛋白基因CsPSP的反义载体构建[J].安徽农业大学学报,2012,39(3):397-400.
作者姓名:龚莹  余梅  江昌俊  吴凡  吉虎  徐凯  臧洁
作者单位:安徽农业大学教育部和农业部茶叶生物化学与生物技术重点实验室;安徽农业大学生命科学学院
基金项目:安徽高校省级自然科学研究重点项目计划(KJ2010A119)资助
摘    要:以茶树龙井43品种的后期花蕾为试验材料,提取总RNA,然后进行RT-PCR得到cDNA第1链。同时,根据GenBank上登录的茶树花粉特异蛋白基因CsPSP(DQ887753)的序列,设计1对特异引物进行PCR反应。将扩增后的基因片段插入pBI121表达载体中,并测序。结果表明,插入pBI121载体的片段长度为318 bp,与已知序列进行比对后一致性达到99.02%,说明载体构建成功。

关 键 词:茶树  CsPSP  反义载体

Antisense vector construction of CsPSP pollen specific protein gene from tea plant (Camellia sinensis L.)
GONG Ying,YU Mei,JIANG Chang-jun,WU Fan,JI Hu,XU Kai and ZANG Jie.Antisense vector construction of CsPSP pollen specific protein gene from tea plant (Camellia sinensis L.)[J].Journal of Anhui Agricultural University,2012,39(3):397-400.
Authors:GONG Ying  YU Mei  JIANG Chang-jun  WU Fan  JI Hu  XU Kai and ZANG Jie
Institution:1.Key Laboratory of Tea Biochemistry and Biotechnology,Ministry of Education and Agriculture, Anhui Agricultural University,Hefei 230036; 2.School of Life Sciences,Anhui Agricultural University,Hefei 230036)
Abstract:In order to study the expression of the pollen-specific gene in tea plant,a pair of specific primers with double enzyme sites was designed to clone a cDNA fragment of CsPSP gene from Longjing43 by the method of RT-PCR,and then the CsPSP fragment was ligated with pBI121 vector and sequenced.The result indicates that the sequence has 99.02% similarity to CsPSP gene in GenBank.
Keywords:Camellia sinensis    CsPSP  antisense vector
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