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F-box蛋白AtSKIP5对气孔对病原体和干旱胁迫反应的调控

Regulation of Stomatal Responses to Pathogen and Drought Stress by the F-Box Protein AtSKIP5.

作者信息

Zhang Ting, Wang Kang, Li Xinyuan, Zhang Cheng, Wang Kui, Zhang Huajian

机构信息

Key Laboratory of Agri-Products Quality and Biosafety (Anhui Agricultural University), Ministry of Education, Hefei, China.

Anhui Province Key Laboratory of Crop Integrated Pest Management, Department of Plant Pathology, College of Plant Protection, Anhui Agricultural University, Hefei, China.

出版信息

Mol Plant Pathol. 2025 Mar;26(3):e70074. doi: 10.1111/mpp.70074.

Abstract

E3 ubiquitin ligases are major components of the ubiquitination cascade and contribute to the stomatal responses to pathogen and drought stress in plants. The F-box SKP1-Interacting Partners (AtSKIPs) proteins are members of the SCF E3 ubiquitin ligase complexes; however, whether they have any involvement in stomatal movement remains unclear. Here, based on tissue expression profiling, we found that the AtSKIP5 protein was highly expressed in guard cells. Mutation of AtSKIP5 rendered plants more susceptible to Pseudomonas syringae pv. tomato (Pst) DC3000 and resulted in a significant impairment in stomatal closure after flg22 and Pst DC3000 treatment. Consistently, lines overexpressing AtSKIP5 were more resistant to Pst DC3000 infection and exhibited more rapid stomatal closure than did other lines. However, the AtSKIP5-overexpressing lines and Col-0 line were similarly resistant to Pst (coronatine-deficient mutant) infection and did not exhibit stomatal reopening when exposed to Pst DC3000, a Pst strain, or a Pst strain accompanied by coronatine (COR) treatment. These results suggest that AtSKIP5-mediated resistance to Pst DC3000 is by controlling stomatal immunity via positive regulation of flg22-triggered stomatal closure and suppression of COR-mediated stomatal reopening. Furthermore, apoplastic immunity was compromised in the skip5 mutants, as evidenced by lower MAPK phosphorylation levels, less reactive oxygen species (ROS) production, and callose deposition induced by flg22, shifting the response in the pathogenic direction. In addition, the skip5 mutants evidenced an impairment in stomatal closure induced by abscisic acid (ABA), and a lower survival rate and greater water loss under drought stress, suggesting that AtSKIP5 serves as a positive regulator of drought tolerance via ABA-induced stomatal closure. Our results provide new insights into the importance of the stomatal responses to pathogen and drought stresses that are modulated by AtSKIP5 in Arabidopsis.

摘要

E3泛素连接酶是泛素化级联反应的主要组成部分,在植物气孔对病原体和干旱胁迫的响应中发挥作用。F-box SKP1相互作用蛋白(AtSKIPs)是SCF E3泛素连接酶复合物的成员;然而,它们是否参与气孔运动仍不清楚。在此,基于组织表达谱分析,我们发现AtSKIP5蛋白在保卫细胞中高表达。AtSKIP5突变使植物对丁香假单胞菌番茄致病变种(Pst)DC3000更敏感,并导致在flg22和Pst DC3000处理后气孔关闭显著受损。一致地,过表达AtSKIP5的株系对Pst DC3000感染更具抗性,并且比其他株系表现出更快的气孔关闭。然而,过表达AtSKIP5的株系和Col-0株系对Pst(冠菌素缺陷型突变体)感染的抗性相似,并且在暴露于Pst DC3000、一种Pst菌株或伴有冠菌素(COR)处理的Pst菌株时未表现出气孔重新开放。这些结果表明,AtSKIP5介导的对Pst DC3000的抗性是通过正向调节flg22触发的气孔关闭和抑制COR介导的气孔重新开放来控制气孔免疫。此外,在skip5突变体中质外体免疫受损,这通过较低的MAPK磷酸化水平、较少的活性氧(ROS)产生以及flg22诱导的胼胝质沉积得以证明,使反应向致病方向转变。此外,skip5突变体在脱落酸(ABA)诱导的气孔关闭方面存在缺陷,并且在干旱胁迫下存活率较低且水分损失更大,表明AtSKIP5通过ABA诱导的气孔关闭作为耐旱性的正向调节因子。我们的结果为拟南芥中AtSKIP5调节的气孔对病原体和干旱胁迫的响应的重要性提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c29c/11906370/5e0f95b5a5d5/MPP-26-e70074-g009.jpg

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