Conserved signaling modules regulate filamentous growth in fungi: a model for eukaryotic cell differentiation.

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2024-10-07 DOI:10.1093/genetics/iyae122
Matthew D Vandermeulen, Michael C Lorenz, Paul J Cullen
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引用次数: 0

Abstract

Eukaryotic organisms are composed of different cell types with defined shapes and functions. Specific cell types are produced by the process of cell differentiation, which is regulated by signal transduction pathways. Signaling pathways regulate cell differentiation by sensing cues and controlling the expression of target genes whose products generate cell types with specific attributes. In studying how cells differentiate, fungi have proved valuable models because of their ease of genetic manipulation and striking cell morphologies. Many fungal species undergo filamentous growth-a specialized growth pattern where cells produce elongated tube-like projections. Filamentous growth promotes expansion into new environments, including invasion into plant and animal hosts by fungal pathogens. The same signaling pathways that regulate filamentous growth in fungi also control cell differentiation throughout eukaryotes and include highly conserved mitogen-activated protein kinase (MAPK) pathways, which is the focus of this review. In many fungal species, mucin-type sensors regulate MAPK pathways to control filamentous growth in response to diverse stimuli. Once activated, MAPK pathways reorganize cell polarity, induce changes in cell adhesion, and promote the secretion of degradative enzymes that mediate access to new environments. However, MAPK pathway regulation is complicated because related pathways can share components with each other yet induce unique responses (i.e. signal specificity). In addition, MAPK pathways function in highly integrated networks with other regulatory pathways (i.e. signal integration). Here, we discuss signal specificity and integration in several yeast models (mainly Saccharomyces cerevisiae and Candida albicans) by focusing on the filamentation MAPK pathway. Because of the strong evolutionary ties between species, a deeper understanding of the regulation of filamentous growth in established models and increasingly diverse fungal species can reveal fundamentally new mechanisms underlying eukaryotic cell differentiation.

真菌中调控丝状生长的保守信号模块:真核细胞分化的模型。
真核生物由不同类型的细胞组成,这些细胞具有明确的形状和功能。特定的细胞类型由细胞分化过程产生,而细胞分化过程受信号转导途径调控。信号传导途径通过感知线索和控制目标基因的表达来调节细胞分化,目标基因的产物产生具有特定属性的细胞类型。在研究细胞如何分化的过程中,真菌因其易于基因操作和引人注目的细胞形态而被证明是有价值的模型。许多真菌物种都经历过丝状生长--一种细胞产生细长管状突起的特殊生长模式。丝状生长促进真菌向新环境扩张,包括真菌病原体入侵动植物宿主。调控真菌丝状生长的信号通路也控制着整个真核生物的细胞分化,其中包括高度保守的丝裂原活化蛋白激酶(MAPK)通路,这也是本综述的重点。在许多真菌物种中,粘蛋白型传感器调节 MAPK 通路,以控制丝状生长,从而对各种刺激做出反应。MAPK 通路一旦被激活,就会重组细胞极性,诱导细胞粘附性发生变化,并促进降解酶的分泌,从而介导细胞进入新环境。然而,MAPK 通路的调控是复杂的,因为相关的通路可以彼此共享成分,但却能诱发独特的反应(即信号特异性)。此外,MAPK 通路在与其他调控通路高度整合的网络中发挥作用(即信号整合)。在这里,我们将通过重点研究丝状 MAPK 通路,讨论几个酵母模型(主要是酿酒酵母和白色念珠菌)中的信号特异性和整合。由于物种之间存在紧密的进化联系,深入了解既有模型和日益多样化的真菌物种的丝状生长调控,可以揭示真核细胞分化的基本新机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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