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柽柳THWRKY12基因的克隆及表达分析 被引量:1

Cloning and Expression Analysis of THWRKY12 Gene in Tamarix hispida
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摘要 [目的]克隆柽柳THWRKY12基因,并对其进行表达分析。[方法]分别用400 mmol/L NaCl溶液、20%PEG及100μmol/L ABA对柽柳幼苗进行胁迫处理后,用RT-PCR技术研究THWRKY12基因在各组织中的表达情况。[结果]在NaCl和PEG处理下,THWRKY12基因在柽柳幼苗各组织中表达总体呈上调趋势,表明该基因与柽柳的抗盐碱及抗旱过程有关;且ABA处理后THWRKY12基因的表达模式与前两者大致相同,表明该基因可能通过ABA调控的信号通路参与柽柳的抗盐碱及抗旱调控。[结论]该研究为研究WRKY基因在柽柳抗逆性中的作用奠定了基础。 [ Objective ] The paper described the cloning and analyses of the expression of THWRKY12 gene from Tamarix hispida. [ Method ] The T. hispida seedlings were treated with 400 mmol/L NaC1 solution ,20% PEG or 100μmol/L ABA respectively. Then the expression of THWRKY12 gene in different tissues was studied by using real-time RT-PCR technology. [ Result] The expression of THWRKY12 gene in different tissues of T. hispida seedlings showed an overall upregulation trend under both the treatment of NaC1 and PEG. It showed that the gene is involved in the process of saline - alkali resistance and drought resistance of T. hispida, treatments,indicating that the gene might involve in the regulation of sa- line stress tolerance and drought resistance of T. hispida through the ABA-dependant signaling pathway. [ Conclusion] The study laid a foundation for the study of the function of WRKY gene in the stress resistance of T. hispida.
出处 《安徽农业科学》 CAS 2013年第14期6147-6148,6187,共3页 Journal of Anhui Agricultural Sciences
基金 东北林业大学大学生创新实验项目(NO.201210225004)
关键词 柽柳 WRKY转录因子 RT-PCR 盐碱胁迫 干旱胁迫 Tamarix hispida WRKY transcription factor RT-PCR Saline-alkali stress Drought stress
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