野生大豆(Glycine soja)转录因子 GsWRKY40 在植物耐盐性中发挥积极作用

Minglong Li, Man Xue, Huiying Ma, Peng Feng, Tong Chen, Xiaohuan Sun, Qiang Li, Xiaodong Ding, Shuzhen Zhang, Jialei Xiao
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引用次数: 0

摘要

野生大豆()是栽培大豆的近缘种,对不利环境条件具有很强的适应性。我们发现并鉴定了一个野生大豆转录因子基因,即 GsWRKY40,它能促进植物盐胁迫。GsWRKY40 定位于细胞核中,具有 DNA 结合活性,但没有转录激活作用。突变和过表达改变了植物的耐盐性。为了解GsWRKY40调控植物耐盐性的分子机制,我们利用酵母双杂交方法筛选了cDNA文库并鉴定出了与GsWRKY40相互作用的蛋白GsbHLH92。通过共免疫沉淀(co-IP)、GST pull-down和双分子荧光互补(BiFC)技术证实了GsWRKY40和GsbHLH92的物理相互作用。耐人寻味的是,在复合大豆植株中,与过表达或相比,共重表达 和 会导致更高的耐盐性和更低的 ROS 水平,这表明 GsWRKY40 和 GsbHLH92 可能通过抑制 ROS 的产生来协同调控植物的耐盐性。qRT-PCR 数据表明,编码过氧化物酶的基因的表达水平受 GsWRKY40 和 GsbHLH92 的协同调控,这一点通过双荧光素酶报告系统和酵母单杂交实验得到了证实。我们的研究揭示了GsWRKY40和GsbHLH92通过阻碍表达和降低ROS水平协同上调植物抗盐性的途径,为植物耐受非生物胁迫的调控机制提供了一个新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Wild soybean (Glycine soja) transcription factor GsWRKY40 plays positive roles in plant salt tolerance
Wild soybean (), a relative of cultivated soybean, shows high adaptability to adverse environmental conditions. We identified and characterized a wild soybean transcription factor gene, , that promotes plant salt stress. was highly expressed in wild soybean roots and was up-regulated by salt treatment. GsWRKY40 was localized in nucleus and demonstrated DNA-binding activities but without transcriptional activation. Mutation and overexpression of altered salt tolerance of plants. To understand the molecular mechanism of GsWRKY40 in regulating plant salt resistance, we screened a cDNA library and identified a GsWRKY40 interacting protein GsbHLH92 by using yeast two-hybrid approach. The physical interaction of GsWRKY40 and GsbHLH92 was confirmed by co-immunoprecipitation (co-IP), GST pull-down, and bimolecular fluorescence complementation (BiFC) techniques. Intriguingly, co-overexpression of and resulted in higher salt tolerance and lower ROS levels than overexpression of or in composite soybean plants, suggesting that GsWRKY40 and GsbHLH92 may synergistically regulate plant salt resistance through inhibiting ROS production. qRT-PCR data indicated that the expression level of gene encoding peroxidase was cooperatively regulated by GsWRKY40 and GsbHLH92, which was confirmed by using a dual luciferase report system and yeast one-hybrid experiment. Our study reveals a pathway that GsWRKY40 and GsbHLH92 collaboratively up-regulate plant salt resistance through impeding expression and reducing ROS levels, providing a novel perspective on the regulatory mechanisms underlying plant tolerance to abiotic stresses.
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