State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Yunnan University, Kunming, China.
Key Laboratory for Microbial Resources of the Ministry of Education, Yunnan University, Kunming, China.
Front Cell Infect Microbiol. 2022 Feb 16;12:754333. doi: 10.3389/fcimb.2022.754333. eCollection 2022.
Arrestins are a family of scaffold proteins that play a crucial role in regulating numerous cellular processes, such as GPCR signaling. The arrestin family contains 12 members, which have highly conserved N-terminal and C-terminal domains. In the presence of ammonia, can change its lifestyle from saprotrophic to carnivorous. During this transition, the expression pattern of arrestin-coding () genes was markedly upregulated. Therefore, we disrupted seven genes from to identify their functions. Although individual arrestin mutant strains display similar pathogenesis, phenotypes, and stress resistance, the fundamental data on the roles of genes in are obtained in this study. Membrane endocytosis in mutants was significantly reduced. Meanwhile, the capacity of trap device formation against nematodes and ammonia was impaired due to deletions. We also found that genes could regulate conidial phenotypes, cell nuclear distribution, pH response, and stress resistance. Results of qRT-PCR assays revealed that sporulation-regulated genes were affected after the deletion of genes. In particular, among the 12 arrestins, mediates pH signaling in the fungus . Notably, combined with the classical paradigm of arrestin-GPCR signal transduction, we suggest that arrestin-regulated trap formation in may be directly linked to the receptor endocytosis pathway.
抑制蛋白是一类支架蛋白,在调节许多细胞过程中起着关键作用,如 G 蛋白偶联受体信号转导。抑制蛋白家族包含 12 个成员,它们具有高度保守的 N 端和 C 端结构域。在氨存在的情况下, 可以将其生活方式从腐生转变为肉食。在这个转变过程中,抑制蛋白编码 () 基因的表达模式显著上调。因此,我们从 中敲除了七个 基因,以确定它们的功能。尽管单个抑制蛋白突变株表现出相似的发病机制、表型和应激抗性,但本研究获得了关于 基因在 中的基本功能数据。在 突变体中,膜内吞作用显著减少。同时,由于 缺失,陷阱装置形成对线虫和氨的能力受损。我们还发现 基因可以调节分生孢子表型、核分布、pH 响应和应激抗性。qRT-PCR 检测结果显示, 基因缺失后,孢子形成调节基因受到影响。特别是在 12 个抑制蛋白中, 介导真菌中的 pH 信号转导。值得注意的是,结合经典的抑制蛋白-GPCR 信号转导范例,我们提出抑制蛋白调节 的陷阱形成可能与受体内吞途径直接相关。