The negative regulated immune mechanism of Skp1-Cullin1-F-box (SCF) E3 ubiquitin ligase-mediated HOS15-dependent responses in banana.

IF 4.5 2区 生物学 Q1 PLANT SCIENCES
Xinyi Chen, Xingchen Jia, Ruizhou Fu, Maoli Wang, Hang Rong, Jinyi Wei, Zishu Wang, Mingyuan Wang
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Abstract

Key message: Under Foc TR4 stress, MaSKP1-1, MaCULI1, and MaHOS15 form SCFHOS15-type E3 ubiquitin ligase, which inhibits the expression level of SA signal-related factors to regulate the immune process of bananas. Banana wilt disease, caused by Fusarium oxysporum f. sp. cubense, tropical race 4 (Foc TR4), poses a significant threat to global banana production. In Musa spp., HOS15 is believed to play a role in enhancing the response to Foc TR4 stress by the salicylic acid signaling pathway. Previous studies have indicated that HOS15 functions as an F-box protein within the SCF ubiquitin ligase complex, contributing to plant biotic stress responses. However, the regulatory mechanisms of SCF in bananas remain poorly understood. In this study, we identified MaSkp1-1 and MaCUL1 as key components in bananas. Under Foc TR4 stress conditions, expression levels of MaSkp1-1 and MaCUL1 increased in the roots of the susceptible variety Williams, whereas their expression decreased in the resistant variety 'Nantianhuang'. The involvement of the MaSkp1-1-MaCUL1-HOS15 module in banana wilt disease was confirmed through yeast two-hybrid assays and bimolecular fluorescence complementation experiments. Arabidopsis thaliana lines overexpressing MaSkp1-1 (MaSkp1 OE) and MaCUL1 (MaCUL1 OE) exhibited reduced resistance to Foc TR4 infection. Furthermore, both MaSkp1-1 and MaCUL1 were found to mediate Arabidopsis's response to Foc TR4 stress by influencing the expression of salicylic acid-related genes. In conclusion, these findings provide new insights into the molecular mechanisms underlying the function of the MaSkp1-1-MaCUL1-HOS15 module in plant responses to Foc TR4 stress.

香蕉Skp1-Cullin1-F-box (SCF) E3泛素连接酶介导的hos15依赖性应答的负调控免疫机制
关键信息:在Foc TR4胁迫下,MaSKP1-1、MaCULI1和MaHOS15形成scfhos15型E3泛素连接酶,抑制SA信号相关因子的表达水平,调节香蕉的免疫过程。香蕉枯萎病是由香蕉尖孢镰刀菌(Fusarium oxysporum f. sp. cubense, tropical race 4, Foc TR4)引起的,对全球香蕉生产构成重大威胁。在Musa spp.中,HOS15被认为通过水杨酸信号通路在增强对Foc TR4胁迫的响应中发挥作用。先前的研究表明,HOS15作为SCF泛素连接酶复合体中的F-box蛋白,参与植物的生物胁迫反应。然而,香蕉中SCF的调控机制仍然知之甚少。在这项研究中,我们确定了MaSkp1-1和MaCUL1是香蕉的关键成分。在Foc TR4胁迫条件下,敏感品种威廉姆斯根系中MaSkp1-1和MaCUL1的表达水平升高,而抗性品种南天黄的表达水平则降低。通过酵母双杂交实验和双分子荧光互补实验,证实了MaSkp1-1-MaCUL1-HOS15模块参与香蕉枯萎病。过表达MaSkp1-1 (MaSkp1 OE)和MaCUL1 (MaCUL1 OE)的拟南芥株系对Foc TR4感染的抗性降低。此外,MaSkp1-1和MaCUL1均通过影响水杨酸相关基因的表达介导拟南芥对Foc TR4胁迫的响应。总之,这些发现为揭示MaSkp1-1-MaCUL1-HOS15模块在植物对Foc TR4胁迫响应中的功能分子机制提供了新的见解。
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来源期刊
Plant Cell Reports
Plant Cell Reports 生物-植物科学
CiteScore
10.80
自引率
1.60%
发文量
135
审稿时长
3.2 months
期刊介绍: Plant Cell Reports publishes original, peer-reviewed articles on new advances in all aspects of plant cell science, plant genetics and molecular biology. Papers selected for publication contribute significant new advances to clearly identified technological problems and/or biological questions. The articles will prove relevant beyond the narrow topic of interest to a readership with broad scientific background. The coverage includes such topics as: - genomics and genetics - metabolism - cell biology - abiotic and biotic stress - phytopathology - gene transfer and expression - molecular pharming - systems biology - nanobiotechnology - genome editing - phenomics and synthetic biology The journal also publishes opinion papers, review and focus articles on the latest developments and new advances in research and technology in plant molecular biology and biotechnology.
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