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遗传调控交配突起在 中的发育。

Genetic regulation of the development of mating projections in .

机构信息

Department of infectious diseases, Huashan Hospital, Fudan University, Shanghai, People's Republic of China.

State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, People's Republic of China.

出版信息

Emerg Microbes Infect. 2020 Feb 21;9(1):413-426. doi: 10.1080/22221751.2020.1729067. eCollection 2020.

Abstract

is a major human fungal pathogen, capable of switching among a range of morphological types, such as the yeast form, including white and opaque cell types and the GUT (gastrointestinally induced transition) cell type, the filamentous form, including hyphal and pseudohyphal cell types, and chlamydospores. This ability is associated with its commensal and pathogenic life styles. In response to pheromone, cells are able to form long mating projections resembling filaments. This filamentous morphology is required for efficient sexual mating. In the current study, we report the genetic regulatory mechanisms controlling the development of mating projections in . Ectopic expression of α1 in "" cells induces the secretion of α-pheromone and promotes the development of mating projections. Using this inducible system, we reveal that members of the pheromone-sensing pathway (including the pheromone receptor), the Ste11-Hst7-Cek1/2 mediated MAPK signalling cascade, and the RAM pathway are essential for the development of mating projections. However, the cAMP/PKA signalling pathway and a number of key regulators of filamentous growth such as Hgc1, Efg1, Flo8, Tec1, Ume6, and Rfg1 are not required for mating projection formation. Therefore, despite the phenotypic similarities between filaments and mating projections in , distinct mechanisms are involved in the regulation of these two morphologies.

摘要

是一种主要的人类真菌病原体,能够在一系列形态类型之间切换,例如酵母形式,包括白色和不透明细胞类型和 GUT(胃肠道诱导转变)细胞类型、丝状形式,包括菌丝和假菌丝细胞类型和厚壁孢子。这种能力与其共生和致病生活方式有关。在响应信息素时,细胞能够形成类似于菌丝的长交配突起。这种丝状形态对于有效进行性交配是必需的。在本研究中,我们报告了控制交配突起发育的遗传调控机制。在“”细胞中外源表达α1会诱导α-信息素的分泌,并促进交配突起的发育。利用这个可诱导系统,我们揭示了信息素感应途径(包括信息素受体)、Ste11-Hst7-Cek1/2 介导的 MAPK 信号级联和 RAM 途径的成员对于交配突起的发育是必需的。然而,cAMP/PKA 信号通路和丝状生长的许多关键调节剂,如 Hgc1、Efg1、Flo8、Tec1、Ume6 和 Rfg1,对于交配突起的形成不是必需的。因此,尽管丝状和交配突起在表型上相似,但在调节这两种形态方面涉及不同的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c15/7048184/c3bc5fa588e8/TEMI_A_1729067_F0001_OC.jpg

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