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杨树抗杨四瘿螨相关基因的表达分析
引用本文:张萍,潘惠新,黄敏仁,王明庥.杨树抗杨四瘿螨相关基因的表达分析[J].南京林业大学学报(自然科学版),2009,0(4):8-12.
作者姓名:张萍  潘惠新  黄敏仁  王明庥
作者单位:南京林业大学,江苏省杨树种质创新与品种改良重点实验室,江苏,南京,210037
基金项目:国家"十一五"科技支撑计划,国家高技术研究发展计划 
摘    要:采用抑制性消减杂交(suppression subtractive hybridization,SSH)技术,在构建杨四瘿螨诱导差异表达的抑制消减cDNA文库的基础上,通过RTPCR技术对候选基因进行了验证,其中有6条差异表达候选基因在4个时间点表达量有明显的增强。运用RACE(Rapid Amplification of cDNA Ends)技术克隆获得了一段全长2 053 bp的cDNA克隆,命名为PtWRKY,编码588个氨基酸。

关 键 词:杨四瘿螨  RTPCR  RACE  PtWRKY

Differentially expressed gene analysis of populus induced by Tetra lobulifera(Keifer)
ZHANG Ping,PAN Hui-xin,HUANG Min-ren,WANG Ming-xiu.Differentially expressed gene analysis of populus induced by Tetra lobulifera(Keifer)[J].Journal of Nanjing Forestry University(Natural Sciences ),2009,0(4):8-12.
Authors:ZHANG Ping  PAN Hui-xin  HUANG Min-ren  WANG Ming-xiu
Institution:Jiangsu Key Laboratory for Poplar Germplasm Enhancement and Variety Improvement, Nanjing Forestry University, Nanjing 210037, China
Abstract:A suppression subtractive hybridization(SSH) cDNA library was constructed with Populus deltoides induced by Tetra lobulifera(Keifer).Real-time PCR was performed to confirm the candidate genes.In this study,six differentially expressed genes were found to be up-regulated.Subsequently,the full-long cDNA sequence about 2 053 bp was cloned by the RACE(Rapid Amplification of cDNA Ends) and named PtWRKY,which encod 588 amino acids.
Keywords:RT-PCR  RACE  PtWRKY
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