在隐球菌真菌中,交替 TSS 的使用非常普遍,它是对环境线索的反应,并受转录因子 Tur1 的全基因组调控。

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences
PLoS Biology Pub Date : 2024-07-25 eCollection Date: 2024-07-01 DOI:10.1371/journal.pbio.3002724
Thi Tuong Vi Dang, Corinne Maufrais, Jessie Colin, Frédérique Moyrand, Isabelle Mouyna, Jean-Yves Coppée, Chinaemerem U Onyishi, Joanna Lipecka, Ida Chiara Guerrera, Robin C May, Guilhem Janbon
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引用次数: 0

摘要

替代转录起始位点(TSS)使用调控已被确定为元动物基因表达调控的一种主要手段。然而,在真菌中,由于迄今为止对它的研究仅限于模式酵母,其影响仍然难以捉摸。在这里,我们首先重新分析了 TSS-seq 数据,以确定 2 种致病隐球菌中真正的 TSS 簇。我们发现了 2 种与特定 DNA 序列图案相关的 TSS 簇。我们的分析还揭示出,隐球菌中普遍存在针对环境线索的替代 TSS 使用调控,从而改变基因表达和蛋白质靶向。重要的是,我们进行了前向遗传筛选,发现了一种名为 Tur1 的独特转录因子(TF),当细胞从指数期转入静止期时,它能调控全基因组的替代 TSS(altTSS)使用。ChiP-Seq和DamID-Seq分析表明,在某些位点,Tur1的作用可能是直接的。Tur1 以前已被证明对 C. neoformans 的毒力至关重要。我们在此证明,与野生型(WT)菌株相比,tur1Δ突变株对超氧化物压力更敏感,被巨噬细胞吞噬的效率更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alternative TSS use is widespread in Cryptococcus fungi in response to environmental cues and regulated genome-wide by the transcription factor Tur1.

Alternative transcription start site (TSS) usage regulation has been identified as a major means of gene expression regulation in metazoans. However, in fungi, its impact remains elusive as its study has thus far been restricted to model yeasts. Here, we first re-analyzed TSS-seq data to define genuine TSS clusters in 2 species of pathogenic Cryptococcus. We identified 2 types of TSS clusters associated with specific DNA sequence motifs. Our analysis also revealed that alternative TSS usage regulation in response to environmental cues is widespread in Cryptococcus, altering gene expression and protein targeting. Importantly, we performed a forward genetic screen to identify a unique transcription factor (TF) named Tur1, which regulates alternative TSS (altTSS) usage genome-wide when cells switch from exponential phase to stationary phase. ChiP-Seq and DamID-Seq analyses suggest that at some loci, the role of Tur1 might be direct. Tur1 has been previously shown to be essential for virulence in C. neoformans. We demonstrated here that a tur1Δ mutant strain is more sensitive to superoxide stress and phagocytosed more efficiently by macrophages than the wild-type (WT) strain.

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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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