Hyperosmolarity-induced suppression of group B1 Raf-like protein kinases modulates drought-growth trade-off in Arabidopsis

IF 9.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Proceedings of the National Academy of Sciences of the United States of America Pub Date : 2024-12-19 DOI:10.1073/pnas.2419204121
Yoshiaki Kamiyama, Sotaro Katagiri, Yangdan Li, Kota Yamashita, Hinano Takase, Taishi Umezawa
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Abstract

When plants are exposed to drought stress, there is a trade-off between plant growth and stress responses. Here, we identified a signaling mechanism for the initial steps of the drought-growth trade-off. Phosphoproteomic profiling revealed that Raf13, a B1 subgroup Raf-like kinase, is dephosphorylated under drought conditions. Raf13 and the related B1-Raf Raf15 are required for growth rather than the acquisition of osmotolerance. We also found that Raf13 interacts with B55-family regulatory subunits of protein phosphatase 2A (PP2A), which mediates hyperosmolarity-induced dephosphorylation of Raf13. In addition, Raf13 interacts with an AGC kinase INCOMPLETE ROOT HAIR ELONGATION HOMOLOG 1 (IREH1), and Raf13 and IREH1 have similar functions in regulating cellular responses that promote plant growth. Overall, our results support a model in which Raf13-IREH1 activity promotes growth under nonstressed conditions, whereas PP2A activity suppresses Raf13-IREH1 during osmotic stress to modulate the physiological “trade-off” between plant growth and stress responses.
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高渗透性诱导的 B1 组 Raf 样蛋白激酶抑制调节拟南芥的干旱-生长权衡
当植物受到干旱胁迫时,在植物生长和胁迫反应之间存在一种权衡。在这里,我们确定了干旱-生长权衡的初始步骤的信号机制。磷酸化蛋白质组学分析显示,在干旱条件下,B1亚群raf样激酶Raf13被去磷酸化。Raf13和相关的B1-Raf Raf15是生长所必需的,而不是获得渗透耐受性。我们还发现,Raf13与蛋白磷酸酶2A (PP2A)的b55家族调控亚基相互作用,介导高渗诱导的Raf13去磷酸化。此外,Raf13与AGC激酶不完全根毛伸长同源物1 (IREH1)相互作用,并且Raf13和IREH1在调节促进植物生长的细胞反应方面具有相似的功能。总的来说,我们的研究结果支持一个模型,即在非胁迫条件下,Raf13-IREH1活性促进生长,而PP2A活性在渗透胁迫下抑制Raf13-IREH1,以调节植物生长和胁迫反应之间的生理“权衡”。
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来源期刊
CiteScore
19.00
自引率
0.90%
发文量
3575
审稿时长
2.5 months
期刊介绍: The Proceedings of the National Academy of Sciences (PNAS), a peer-reviewed journal of the National Academy of Sciences (NAS), serves as an authoritative source for high-impact, original research across the biological, physical, and social sciences. With a global scope, the journal welcomes submissions from researchers worldwide, making it an inclusive platform for advancing scientific knowledge.
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