Suppr超能文献

GmMKK4 激活的 GmMPK6 刺激 GmERF113 触发大豆对大豆疫霉的抗性。

GmMKK4-activated GmMPK6 stimulates GmERF113 to trigger resistance to Phytophthora sojae in soybean.

机构信息

Soybean Research Institute, Northeast Agricultural University/Key Laboratory of Soybean Biology of Chinese Education Ministry, Harbin, 150030, China.

Jilin Agricultural University, Changchun, 130118, China.

出版信息

Plant J. 2022 Jul;111(2):473-495. doi: 10.1111/tpj.15809. Epub 2022 Jun 2.

Abstract

Phytophthora root and stem rot is a worldwide soybean (Glycine max) disease caused by the soil-borne pathogen Phytophthora sojae. This disease is devastating to soybean production, so improvement of resistance to P. sojae is a major target in soybean breeding. Mitogen-activated protein kinase (MAPK) cascades are important signaling modules that convert environmental stimuli into cellular responses. Compared with extensive studies in Arabidopsis, the molecular mechanism of MAPK cascades in soybean disease resistance is barely elucidated. In this work, we found that the gene expression of mitogen-activated protein kinase 6 (GmMPK6) was potently induced by P. sojae infection in the disease-resistant soybean cultivar 'Suinong 10'. Overexpression of GmMPK6 in soybean resulted in enhanced resistance to P. sojae and silencing of GmMPK6 led to the opposite phenotype. In our attempt to dissect the role of GmMPK6 in soybean resistance to phytophthora disease, we found that MAPK kinase 4 (GmMKK4) and the ERF transcription factor GmERF113 physically interact with GmMPK6, and we determined that GmMKK4 could phosphorylate and activate GmMPK6, which could subsequently phosphorylate GmERF113 upon P. sojae infection, suggesting that P. sojae can stimulate the GmMKK4-GmMPK6-GmERF113 signaling pathway in soybean. Moreover, phosphorylation of GmERF113 by the GmMKK4-GmMPK6 module promoted GmERF113 stability, nuclear localization and transcriptional activity, which significantly enhanced expression of the defense-related genes GmPR1 and GmPR10-1 and hence improved disease resistance of the transgenic soybean seedlings. In all, our data reveal that the GmMKK4-GmMPK6-GmERF113 cascade triggers resistance to P. sojae in soybean and shed light on functions of MAPK kinases in plant disease resistance.

摘要

大豆疫霉根腐茎腐病是一种世界性大豆病害,由土传病原菌大豆疫霉引起。该病害对大豆生产危害极大,因此提高大豆对疫霉的抗性是大豆育种的主要目标。丝裂原活化蛋白激酶(MAPK)级联是将环境刺激转化为细胞反应的重要信号模块。与拟南芥的广泛研究相比,MAPK 级联在大豆抗病性中的分子机制几乎没有得到阐明。在这项工作中,我们发现抗病大豆品种‘苏农 10’中,大豆丝裂原活化蛋白激酶 6(GmMPK6)的基因表达受大豆疫霉侵染的强烈诱导。大豆中 GmMPK6 的过表达导致对大豆疫霉的抗性增强,而 GmMPK6 的沉默则导致相反的表型。在试图剖析 GmMPK6 在大豆对疫霉病抗性中的作用时,我们发现 MAPK 激酶 4(GmMKK4)和 ERF 转录因子 GmERF113 与 GmMPK6 发生物理相互作用,并确定 GmMKK4 可以磷酸化并激活 GmMPK6,GmMPK6 随后在大豆疫霉侵染时磷酸化 GmERF113,这表明大豆疫霉可以在大豆中刺激 GmMKK4-GmMPK6-GmERF113 信号通路。此外,GmMKK4-GmMPK6 模块对 GmERF113 的磷酸化促进了 GmERF113 的稳定性、核定位和转录活性,从而显著增强了防御相关基因 GmPR1 和 GmPR10-1 的表达,进而提高了转基因大豆幼苗的抗病性。总之,我们的数据揭示了 GmMKK4-GmMPK6-GmERF113 级联触发了大豆对大豆疫霉的抗性,并阐明了 MAPK 激酶在植物抗病性中的功能。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验