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C 组 Raf 样蛋白激酶负调控脱落酸信号转导,是 SnRK2 的直接底物。

group C Raf-like protein kinases negatively regulate abscisic acid signaling and are direct substrates of SnRK2.

机构信息

Graduate School of Bio-Applications and Systems Engineering, Tokyo University of Agriculture and Technology, Tokyo 184-8588, Japan.

Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR 97331.

出版信息

Proc Natl Acad Sci U S A. 2021 Jul 27;118(30). doi: 10.1073/pnas.2100073118.

Abstract

The phytohormone abscisic acid (ABA) plays a major role in abiotic stress responses in plants, and subclass III SNF1-related protein kinase 2 (SnRK2) kinases mediate ABA signaling. In this study, we identified Raf36, a group C Raf-like protein kinase in , as a protein that interacts with multiple SnRK2s. A series of reverse genetic and biochemical analyses revealed that 1) Raf36 negatively regulates ABA responses during postgermination growth, 2) the N terminus of Raf36 is directly phosphorylated by SnRK2s, and 3) Raf36 degradation is enhanced in response to ABA. In addition, Raf22, another C-type Raf-like kinase, functions partially redundantly with Raf36 to regulate ABA responses. A comparative phosphoproteomic analysis of ABA-induced responses of wild-type and plants identified proteins that are phosphorylated downstream of Raf36 and Raf22 in planta. Together, these results support a model in which Raf36/Raf22 function mainly under optimal conditions to suppress ABA responses, whereas in response to ABA, the SnRK2 module promotes Raf36 degradation as a means of alleviating Raf36-dependent inhibition and allowing for heightened ABA signaling to occur.

摘要

植物激素脱落酸(ABA)在植物的非生物胁迫反应中起着重要作用,亚类 III SNF1 相关蛋白激酶 2(SnRK2)激酶介导 ABA 信号转导。在这项研究中,我们鉴定出拟南芥中的 Raf36,一种 C 组 Raf 样蛋白激酶,是与多个 SnRK2 相互作用的蛋白。一系列反向遗传学和生化分析表明:1)Raf36 在萌发后生长过程中负调控 ABA 反应;2)Raf36 的 N 端被 SnRK2s 直接磷酸化;3)Raf36 在响应 ABA 时被增强降解。此外,另一种 C 型 Raf 样激酶 Raf22 与 Raf36 部分冗余地发挥作用以调节 ABA 反应。对野生型和 植物 ABA 诱导反应的比较磷酸蛋白质组学分析鉴定了 Raf36 和 Raf22 在植物体内下游磷酸化的蛋白质。总之,这些结果支持了这样的模型,即 Raf36/Raf22 主要在最佳条件下发挥作用以抑制 ABA 反应,而在响应 ABA 时,SnRK2 模块促进 Raf36 降解,作为减轻 Raf36 依赖性抑制并允许增强 ABA 信号转导发生的一种手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fbd/8325330/3c3e86280396/pnas.2100073118fig01.jpg

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