作物学报 ›› 2011, Vol. 37 ›› Issue (09): 1551-1558.doi: 10.3724/SP.J.1006.2011.01551
周凯,叶武威*,王俊娟,王德龙,樊保香,王帅
ZHOU Kai,YE Wu-Wei*,WANG Jun-Juan,WANG De-Long,FAN Bao-Xiang,WANG Shuai
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。
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