马铃薯StFtsH4蛋白抑制植物抗病性研究进展

IF 4.8 1区 农林科学 Q1 PLANT SCIENCES
Siyu Xiao, Jinhui Wang, Zihan Bai, Haibin Jiang, Jiehua Zhu, Zhihui Yang
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引用次数: 0

摘要

茄疫病是马铃薯早疫病的重要坏死性致病菌。然而,茄蚜的致病分子机制尚不清楚。先前的工作通过多组学分析确定了茄属植物的特异性效应因子AsCEP20。AsCEP20是茄茄的全部毒力所必需的,并且靶向宿主叶绿体。在这项研究中,我们利用免疫共沉淀和液相色谱-串联质谱分析筛选出了46个可能与烟叶中AsCEP20相互作用的候选蛋白。基于同源比对和亚细胞定位分析,我们在马铃薯中发现了一个候选靶蛋白——丝状温度敏感蛋白H4 (StFtsH4),该蛋白位于叶绿体中。通过共免疫沉淀、酵母双杂交实验和双分子荧光互补实验进一步证实了AsCEP20与StFtsH4的相互作用。AsCEP20和StFtsH4之间的相互作用位点也是叶绿体。沉默马铃薯StFtsH4基因导致病原体相关分子模式触发的活性氧(ROS)爆发受到抑制,防御相关基因显著下调。这些结果表明,StFtsH4正调控植物免疫。因此,AsCEP20靶向叶绿体蛋白StFtsH4促进病原体感染。AsCEP20通过靶向StFtsH4降低光合作用中光能利用的效率。这些结果表明,AsCEP20抑制stftsh4介导的马铃薯对茄蚜的抗性。随着光照强度的增加,stftsh4沉默植物叶片的叶绿体中ROS持续积累,防御相关基因显著减少。我们的研究结果表明,受损的StFtsH4功能限制了植物的光合作用,从而影响免疫信号传导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alternaria solani Effector AsCEP20, Essential for Virulence, Targets Potato StFtsH4 Protein to Suppress Plant Disease Resistance.

Alternaria solani is an important necrotrophic pathogen causing potato early blight. However, the pathogenic molecular mechanisms of A. solani remain unclear. Previous work identified a specific effector AsCEP20 in A. solani through multi-omics analysis. AsCEP20 is required for the full virulence of A. solani and targets the host chloroplasts. In this study, we screened out 46 candidate proteins that potentially interact with AsCEP20 in Nicotiana benthamiana using co-immunoprecipitation followed by liquid chromatography-tandem mass spectrometry analysis. We identified a candidate target protein in potato, filamentation temperature-sensitive H4 (StFtsH4), which is located in chloroplasts, based on homologous alignment and subcellular localisation analysis. The interaction between AsCEP20 and StFtsH4 was further confirmed by co-immunoprecipitation, yeast two-hybrid assay and bimolecular fluorescence complementation assays. The interaction site between AsCEP20 and StFtsH4 is also the chloroplast. Silencing the potato StFtsH4 gene resulted in suppressed pathogen-associated molecular pattern-triggered reactive oxygen species (ROS) bursts, and defence-related genes were significantly downregulated. These results suggest that StFtsH4 positively regulates plant immunity. Therefore, AsCEP20 targets the chloroplast protein StFtsH4 to promote pathogen infection. AsCEP20 attenuates the efficiency of light energy utilisation in photosynthesis by targeting StFtsH4. These results suggest that AsCEP20 suppresses StFtsH4-mediated potato disease resistance to A. solani. With the increase of light intensity, ROS continued to accumulate in the chloroplast of StFtsH4-silenced plant leaves, while defence-related genes significantly decreased. Our findings reveal that the impaired StFtsH4 function limits plant photosynthesis, thereby affecting immune signalling.

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来源期刊
Molecular plant pathology
Molecular plant pathology 生物-植物科学
CiteScore
9.40
自引率
4.10%
发文量
120
审稿时长
6-12 weeks
期刊介绍: Molecular Plant Pathology is now an open access journal. Authors pay an article processing charge to publish in the journal and all articles will be freely available to anyone. BSPP members will be granted a 20% discount on article charges. The Editorial focus and policy of the journal has not be changed and the editorial team will continue to apply the same rigorous standards of peer review and acceptance criteria.
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