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线虫诱捕真菌节丛孢激活线粒体并重新编程真菌细胞以捕食线虫。

GprC of the nematode-trapping fungus Arthrobotrys flagrans activates mitochondria and reprograms fungal cells for nematode hunting.

机构信息

Department of Microbiology, Institute for Applied Biosciences, Karlsruhe Institute of Technology (KIT) - South Campus, Karlsruhe, Germany.

Department of Theoretical Chemical Biology, Institute for Physical Chemistry, Karlsruhe Institute of Technology (KIT) - South Campus, Karlsruhe, Germany.

出版信息

Nat Microbiol. 2024 Jul;9(7):1752-1763. doi: 10.1038/s41564-024-01731-9. Epub 2024 Jun 14.

DOI:10.1038/s41564-024-01731-9
PMID:38877225
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11222155/
Abstract

Initiation of development requires differential gene expression and metabolic adaptations. Here we show in the nematode-trapping fungus, Arthrobotrys flagrans, that both are achieved through a dual-function G-protein-coupled receptor (GPCR). A. flagrans develops adhesive traps and recognizes its prey, Caenorhabditis elegans, through nematode-specific pheromones (ascarosides). Gene-expression analyses revealed that ascarosides activate the fungal GPCR, GprC, at the plasma membrane and together with the G-protein alpha subunit GasA, reprograms the cell. However, GprC and GasA also reside in mitochondria and boost respiration. This dual localization of GprC in A. flagrans resembles the localization of the cannabinoid receptor CB1 in humans. The C. elegans ascaroside-sensing GPCR, SRBC66 and GPCRs of many fungi are also predicted for dual localization, suggesting broad evolutionary conservation. An SRBC64/66-GprC chimaeric protein was functional in A. flagrans, and C. elegans SRBC64/66 and DAF38 share ascaroside-binding sites with the fungal GprC receptor, suggesting 400-million-year convergent evolution.

摘要

启动发育需要差异基因表达和代谢适应。在这里,我们在食线虫真菌节丛孢菌中表明,这两者都是通过双重功能的 G 蛋白偶联受体(GPCR)实现的。节丛孢菌通过线虫特异性信息素(ascarosides)形成粘性陷阱并识别其猎物秀丽隐杆线虫。基因表达分析表明,ascarosides 在质膜上激活真菌 GPCR GprC,并与 G 蛋白α亚基 GasA 一起重新编程细胞。然而,GprC 和 GasA 也存在于线粒体中并促进呼吸。GprC 在节丛孢菌中的这种双重定位类似于大麻素受体 CB1 在人类中的定位。秀丽隐杆线虫的 ascaroside 感应 GPCR SRBC66 和许多真菌的 GPCR 也被预测为双重定位,表明广泛的进化保守性。SRBC64/66-GprC 嵌合蛋白在节丛孢菌中具有功能,并且秀丽隐杆线虫的 SRBC64/66 和 DAF38 与真菌 GprC 受体共享 ascaroside 结合位点,表明这是 4 亿年来的趋同进化。

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