The Ras GTPase-activating protein UvGap1 orchestrates conidiogenesis and pathogenesis in the rice false smut fungus Ustilaginoidea virens
文献类型: 外文期刊
第一作者: Cao, Huijuan
作者: Cao, Huijuan;Gong, Hao;Yu, Mina;Pan, Xiayan;Song, Tianqiao;Yu, Junjie;Qi, Zhongqiang;Du, Yan;Zhang, Rongsheng;Liu, Yongfeng;Liu, Yongfeng
作者机构:
关键词: conidiation; pathogenicity; Ras GTPase-activating protein; Ustilaginoidea virens
期刊名称:MOLECULAR PLANT PATHOLOGY ( 影响因子:4.9; 五年影响因子:5.9 )
ISSN: 1464-6722
年卷期: 2024 年 25 卷 3 期
页码:
收录情况: SCI
摘要: Ras GTPase-activating proteins (Ras GAPs) act as negative regulators for Ras proteins and are involved in various signalling processes that influence cellular functions. Here, the function of four Ras GAPs, UvGap1 to UvGap4, was identified and analysed in Ustilaginoidea virens, the causal agent of rice false smut disease. Disruption of UvGAP1 or UvGAP2 resulted in reduced mycelial growth and an increased percentage of larger or dumbbell-shaped conidia. Notably, the mutant Delta Uvgap1 completely lost its pathogenicity. Compared to the wild-type strain, the mutants Delta Uvgap1, Delta Uvgap2 and Delta Uvgap3 exhibited reduced tolerance to H2O2 oxidative stress. In particular, the Delta Uvgap1 mutant was barely able to grow on the H2O2 plate, and UvGAP1 was found to influence the expression level of genes involved in reactive oxygen species synthesis and scavenging. The intracellular cAMP level in the Delta Uvgap1 mutant was elevated, as UvGap1 plays an important role in maintaining the intracellular cAMP level by affecting the expression of phosphodiesterases, which are linked to cAMP degradation in U. virens. In a yeast two-hybrid assay, UvRas1 and UvRasGef (Ras guanyl nucleotide exchange factor) physically interacted with UvGap1. UvRas2 was identified as an interacting partner of UvGap1 through a bimolecular fluorescence complementation assay and affinity capture-mass spectrometry analysis. Taken together, these findings suggest that the UvGAP1-mediated Ras pathway is essential for the development and pathogenicity of U. virens.
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