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转录因子 HAT1 是 SnRK2.3 激酶的底物,在拟南芥响应干旱时负调控 ABA 的合成和信号转导。

Transcription factor HAT1 is a substrate of SnRK2.3 kinase and negatively regulates ABA synthesis and signaling in Arabidopsis responding to drought.

机构信息

Key Laboratory of Bio-Resource and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, Sichuan, P.R. China.

Department of Genetics, Development, and Cell Biology, Iowa State University, Ames, IA, United States of America.

出版信息

PLoS Genet. 2018 Apr 16;14(4):e1007336. doi: 10.1371/journal.pgen.1007336. eCollection 2018 Apr.

Abstract

Drought is a major threat to plant growth and crop productivity. The phytohormone abscisic acid (ABA) plays a critical role in plant response to drought stress. Although ABA signaling-mediated drought tolerance has been widely investigated in Arabidopsis thaliana, the feedback mechanism and components negatively regulating this pathway are less well understood. Here we identified a member of Arabidopsis HD-ZIP transcription factors HAT1 which can interacts with and be phosphorylated by SnRK2s. hat1hat3, loss-of-function mutant of HAT1 and its homolog HAT3, was hypersensitive to ABA in primary root inhibition, ABA-responsive genes expression, and displayed enhanced drought tolerance, whereas HAT1 overexpressing lines were hyposensitive to ABA and less tolerant to drought stress, suggesting that HAT1 functions as a negative regulator in ABA signaling-mediated drought response. Furthermore, expression levels of ABA biosynthesis genes ABA3 and NCED3 were repressed by HAT1 directly binding to their promoters, resulting in the ABA level was increased in hat1hat3 and reduced in HAT1OX lines. Further evidence showed that both protein stability and binding activity of HAT1 was repressed by SnRK2.3 phosphorylation. Overexpressing SnRK2.3 in HAT1OX transgenic plant made a reduced HAT1 protein level and suppressed the HAT1OX phenotypes in ABA and drought response. Our results thus establish a new negative regulation mechanism of HAT1 which helps plants fine-tune their drought responses.

摘要

干旱是植物生长和作物生产力的主要威胁。植物激素脱落酸(ABA)在植物对干旱胁迫的反应中起着关键作用。尽管 ABA 信号转导介导的耐旱性已在拟南芥中得到广泛研究,但负调控该途径的反馈机制和组件了解较少。在这里,我们鉴定了拟南芥 HD-ZIP 转录因子 HAT1 的一个成员,它可以与 SnRK2s 相互作用并被其磷酸化。hat1hat3,HAT1 的功能丧失突变体及其同源物 HAT3,对 ABA 在主根抑制、ABA 响应基因表达中的抑制作用更为敏感,表现出增强的耐旱性,而 HAT1 过表达系对 ABA 更为敏感,对干旱胁迫的耐受性降低,表明 HAT1 作为 ABA 信号转导介导的干旱反应中的负调节剂发挥作用。此外,ABA 生物合成基因 ABA3 和 NCED3 的表达水平被 HAT1 直接结合到它们的启动子上抑制,导致 hat1hat3 中的 ABA 水平升高,而 HAT1OX 系中的 ABA 水平降低。进一步的证据表明,HAT1 的蛋白稳定性和结合活性均受到 SnRK2.3 磷酸化的抑制。在 HAT1OX 转基因植物中过表达 SnRK2.3 会降低 HAT1 蛋白水平,并抑制 ABA 和干旱反应中 HAT1OX 表型。因此,我们的研究结果建立了 HAT1 的一个新的负调控机制,有助于植物精细调控其干旱反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e3/5919683/b4005ae0c851/pgen.1007336.g001.jpg

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