RasGEF MoCdc25调控稻瘟病菌的营养生长、萌发和附着胞介导的侵染

IF 2.4 3区 生物学 Q3 GENETICS & HEREDITY Fungal Genetics and Biology Pub Date : 2023-10-01 DOI:10.1016/j.fgb.2023.103825
Yu Xiao, Wuyun Lv, Qi Tong, Zhe Xu, Zhengyi Wang
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引用次数: 0

摘要

Ras鸟嘌呤核苷酸交换因子(RasGEFs)可以触发Ras-GTP酶活性,并在控制真核生物的各种细胞过程中发挥重要作用。最近,研究表明RasGEF-Cdc25调节几种植物病原真菌的形态分化和致病性。然而,RasGEFs在稻瘟病菌中的作用在很大程度上是未知的。在本研究中,我们在米曲霉中鉴定了一个RasGEF基因MoCDC25,并对其进行了功能鉴定,该基因与酿酒酵母CDC25同源。靶向基因缺失突变体(ΔMocdc25)完全无致病性,在菌丝生长、分生孢子和附着胞形成方面受到严重损害。突变体对渗透、细胞壁完整性或氧化应激表现出高度敏感的反应。在酵母双杂交分析中,MoCdc25与MAPK支架Mst50和推定的Cdc42GEF MoScd1物理相互作用。此外,我们发现MoCdc25参与调节MAP激酶(Pmk1、Mps1和Osm1)的磷酸化。此外,与亲本菌株Ku80相比,ΔMocdc25突变体菌丝中的细胞内cAMP含量显著降低,并且通过补充外源cAMP可以部分恢复突变体附着胞形成的缺陷。总之,我们得出结论,RasGEF-MoCdc25通过MAPK和cAMP反应途径调节米霉的营养生长、分生孢子、附着胞形成和致病性。
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The RasGEF MoCdc25 regulates vegetative growth, conidiation and appressorium-mediated infection in the rice blast fungus Magnaporthe oryzae

Ras guanine nucleotide exchange factors (RasGEFs) can trigger Ras GTPase activities and play important roles in controlling various cellular processes in eukaryotes. Recently, it has been exhibited that RasGEF Cdc25 regulates morphological differentiation and pathogenicity in several plant pathogenic fungi. However, the role of RasGEFs in Magnaporthe oryzae is largely unknown. In this study, we identified and functionally characterized a RasGEF gene MoCDC25 in M. oryzae, which is orthologous to Saccharomyces cerevisiae CDC25. Targeted gene deletion mutants (ΔMocdc25) were completely nonpathogenic and were severely impaired in hyphal growth, conidiation and appressorium formation. The mutants exhibited highly sensitive response to osmotic, cell wall integrity or oxidative stresses. MoCdc25 physically interacts with the MAPK scaffold Mst50 and the putative Cdc42GEF MoScd1 in yeast two-hybrid assays. Moreover, we found that MoCdc25 was involved in regulating the phosphorylation of the MAP kinases (Pmk1, Mps1, and Osm1). In addition, the intracellular cAMP content in hyphae of the ΔMocdc25 mutants was significantly reduced compared to the parent strain Ku80 and the defect of appressorium formation of the mutants could be partially restored by the supplement of exogenous cAMP. Taken together, we conclude that the RasGEF MoCdc25 regulates vegetative growth, conidiation, appressorium formation and pathogenicity via MAPK and cAMP response pathways in M. oryzae.

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来源期刊
Fungal Genetics and Biology
Fungal Genetics and Biology 生物-遗传学
CiteScore
6.20
自引率
3.30%
发文量
66
审稿时长
85 days
期刊介绍: Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny. Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists. Research Areas include: • Biochemistry • Cytology • Developmental biology • Evolutionary biology • Genetics • Molecular biology • Phylogeny • Physiology.
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