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小麦 CBL 相互作用蛋白激酶 25 负调控转基因小麦的耐盐性。

Wheat CBL-interacting protein kinase 25 negatively regulates salt tolerance in transgenic wheat.

机构信息

The Genetic Engineering International Cooperation Base of Chinese Ministry of Science and Technology, The Key Laboratory of Molecular Biophysics of Chinese Ministry of Education, College of Life Science and Technology, Huazhong University of Science &Technology, Wuhan 430074, China.

出版信息

Sci Rep. 2016 Jun 30;6:28884. doi: 10.1038/srep28884.

Abstract

CBL-interacting protein kinases are involved in plant responses to abiotic stresses, including salt stress. However, the negative regulating mechanism of this gene family in response to salinity is less reported. In this study, we evaluated the role of TaCIPK25 in regulating salt response in wheat. Under conditions of high salinity, TaCIPK25 expression was markedly down-regulated in roots. Overexpression of TaCIPK25 resulted in hypersensitivity to Na(+) and superfluous accumulation of Na(+) in transgenic wheat lines. TaCIPK25 expression did not decline in transgenic wheat and remained at an even higher level than that in wild-type wheat controls under high-salinity treatment. Furthermore, transmembrane Na(+)/H(+) exchange was impaired in the root cells of transgenic wheat. These results suggested that TaCIPK25 negatively regulated salt response in wheat. Additionally, yeast-one-hybrid, β-glucuronidase activity and DNA-protein-interaction-enzyme-linked-immunosorbent assays showed that the transcription factor TaWRKY9 bound W-box in the TaCIPK25 promoter region. Quantitative real-time polymerase chain reaction assays showed concomitantly inverted expression patterns of TaCIPK25 and TaWRKY9 in wheat roots under salt treatment, ABA application and inhibition of endogenous ABA condition. Overall, based on our results, in a salt stress condition, the negative salt response in wheat involved TaCIPK25 with the expression regulated by TaWRKY9.

摘要

CBL 相互作用蛋白激酶参与植物对非生物胁迫的反应,包括盐胁迫。然而,该基因家族在响应盐胁迫方面的负调控机制报道较少。在这项研究中,我们评估了 TaCIPK25 在调节小麦盐响应中的作用。在高盐条件下,TaCIPK25 在根中的表达明显下调。过表达 TaCIPK25 导致转基因小麦系对 Na(+)敏感和 Na(+)过度积累。在高盐处理下,转基因小麦中的 TaCIPK25 表达没有下降,甚至保持在比野生型小麦对照更高的水平。此外,转基因小麦根细胞中的跨膜 Na(+)/H(+)交换受到损害。这些结果表明 TaCIPK25 负调控小麦的盐响应。此外,酵母单杂交、β-葡萄糖醛酸酶活性和 DNA-蛋白相互作用酶联免疫吸附测定表明,转录因子 TaWRKY9 结合 TaCIPK25 启动子区域的 W 框。定量实时聚合酶链反应分析显示,在盐处理、ABA 应用和抑制内源性 ABA 条件下,小麦根中 TaCIPK25 和 TaWRKY9 的表达模式相反。总的来说,根据我们的结果,在盐胁迫条件下,小麦的负盐响应涉及 TaCIPK25,其表达受 TaWRKY9 调控。

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