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陆地棉质体转录活性因子基因GhPTAC的克隆及其耐盐性分析
引用本文:周凯,叶武威,王俊娟,王德龙,樊保香,王帅. 陆地棉质体转录活性因子基因GhPTAC的克隆及其耐盐性分析[J]. 作物学报, 2011, 37(9): 1551-1558. DOI: 10.3724/SP.J.1006.2011.01551
作者姓名:周凯  叶武威  王俊娟  王德龙  樊保香  王帅
作者单位:中国农业科学院棉花研究所 / 棉花生物学国家重点实验室 / 农业部棉花遗传改良重点实验室,河南安阳 455000
基金项目:国家转基因生物新品种培育科技重大专项(2008ZX08005-004); 国家“十一五”科技支撑计划项目(2006BAD13B04-1)资助
摘    要:为了挖掘新的耐盐基因及调控途径,利用基因芯片技术及抑制性差减文库技术筛选到质体转录活性因子,通过RACE及RT-PCR技术克隆到该基因的cDNA全长,命名为GhPTAC。该cDNA全长1 564 bp,其中ORF 1 038 bp,推测编码345个氨基酸残基的多肽。生物信息学分析表明GhPTAC为拟南芥PTAC13同源基因,同源性60.6%。编码蛋白为转录活跃的染色体(TAC)的一个组分,参与叶绿体基因组转录终止/抗终止调节。Real-time PCR分析结果表明,GhPTAC受盐胁迫诱导上调表达,在耐盐材料中9806中表达水平明显高于盐敏感材料中S9612,这与芯片结果一致。

关 键 词:陆地棉  盐胁迫  PTAC  Real-time PCR
收稿时间:2011-02-28

Cloning and Salt-tolerance Analysis of Gene Plastid Transcriptionally Active(GhPTAC) from Gossypium hirsutum L.
ZHOU Kai,YE Wu-Wei,WANG Jun-Juan,WANG De-Long,FAN Bao-Xiang, WANG Shuai Cotton Research Institute,Chinese Academy of Agricultural Science/State Key Laboratory of Cotton Biology /Key Laboratory of Cotton Genetic Improvement of Agriculture Ministry,Anyang ,China. Cloning and Salt-tolerance Analysis of Gene Plastid Transcriptionally Active(GhPTAC) from Gossypium hirsutum L.[J]. Acta Agronomica Sinica, 2011, 37(9): 1551-1558. DOI: 10.3724/SP.J.1006.2011.01551
Authors:ZHOU Kai  YE Wu-Wei  WANG Jun-Juan  WANG De-Long  FAN Bao-Xiang   WANG Shuai Cotton Research Institute  Chinese Academy of Agricultural Science/State Key Laboratory of Cotton Biology /Key Laboratory of Cotton Genetic Improvement of Agriculture Ministry  Anyang   China
Affiliation:Cotton Research Institute, Chinese Academy of Agricultural Science / State Key Laboratory of Cotton Biology / Key Laboratory of Cotton Genetic Improvement of Agriculture Ministry, Anyang 455000, China
Abstract:To develop novel salt-tolerance genes and adjustment pathway,we screened out gene Plastid Transcriptionally Active named as GhPTAC based on salt-tolerance gene chips and salt resistance related SSH library.The result of RACE and RT-PCR showed that the cDNA full length was 1 564 bp,and ORF was 1 038 bp,which encoded 345 amino acid residues.Bioinformatics analysis showed that GhPTAC shared the identity of 60.6% with the homologous gene PTAC13 from Arabidopsis thaliana.As one part of Transcriptionally active c...
Keywords:Gossypium hirsutum  Salt stress  PTAC  real-time PCR  
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