p体因子在白色念珠菌丝化和应激反应中的作用。

IF 3.9 2区 生物学 Q1 GENETICS & HEREDITY PLoS Genetics Pub Date : 2025-03-17 eCollection Date: 2025-03-01 DOI:10.1371/journal.pgen.1011632
Melissa A Tosiano, Frederick Lanni, Aaron P Mitchell, C Joel McManus
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引用次数: 0

摘要

菌丝生长与人类真菌病原体白色念珠菌的毒力密切相关。虽然菌丝转录网络一直是密集研究的主题,但对转录后调控的了解相对较少。先前的研究报道了p体(PB)因子Dhh1和Edc3是白色念珠菌毒力和丝化所必需的,表明在这些过程的转录后调控中起重要作用。然而,这些因素的分子作用尚未确定。为了进一步研究PB因子在成丝中的功能,我们利用瞬时CRISPR-Cas9技术在多种原生营养临床菌株中产生了DHH1和EDC3的纯合缺失。在五种菌株背景下,纯合DHH1缺失严重损害了生长,改变了细丝,并表现出不同寻常的菌落形态。通过RNA-seq,我们发现在SC5314和P57055中,DHH1缺失破坏了酵母和菌丝生长条件下数千个基因的调控。这包括在没有外部压力的情况下许多应激反应基因的上调,类似于酿酒葡萄球菌DHH1同源物的缺失。相反,我们发现EDC3在不同的菌株中并不需要耐热性或成丝性。这些结果支持了一个模型,即DHH1而不是EDC3抑制酵母菌丝胁迫反应转录本,并在成丝过程中重塑转录组。我们的工作支持对特定mRNA衰变因子的不同要求,支持白色念珠菌转录后丝化调节的证据。
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Roles of P-body factors in Candida albicans filamentation and stress response.

Hyphal growth is strongly associated with virulence in the human fungal pathogen Candida albicans. While hyphal transcriptional networks have been the subject of intense study, relatively little is known about post-transcriptional regulation. Previous work reported that P-Body (PB) factors Dhh1 and Edc3 were required for C. albicans virulence and filamentation, suggesting an essential role for post-transcriptional regulation of these processes. However, the molecular roles of these factors have not been determined. To further study the function of PB factors in filamentation, we generated homozygous deletions of DHH1 and EDC3 in diverse prototrophic clinical strains using transient CRISPR-Cas9. Homozygous DHH1 deletion strongly impaired growth, altered filamentation, and exhibited unusual colony morphology in response to heat stress in five strain backgrounds. Using RNA-seq, we found DHH1 deletion disrupts the regulation of thousands of genes under both yeast and hyphal growth conditions in SC5314 and P57055. This included upregulation of many stress response genes in the absence of external stress, similar to deletion of the S. cerevisiae DHH1 homolog. In contrast, we found EDC3 was not required for heat tolerance or filamentation in diverse strains. These results support a model in which DHH1, but not EDC3, represses hyphal stress response transcripts in yeast and remodels the transcriptome during filamentation. Our work supports distinct requirements for specific mRNA decay factors, bolstering evidence for post-transcriptional regulation of filamentation in C. albicans.

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PLoS Genetics
PLoS Genetics GENETICS & HEREDITY-
自引率
2.20%
发文量
438
期刊介绍: PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill). Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.
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