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在碱性pH条件下,真菌病原体增殖与防御之间的权衡由转录因子GAT201控制。

A trade-off between proliferation and defense in the fungal pathogen at alkaline pH is controlled by the transcription factor GAT201.

作者信息

Hughes Elizabeth S, Tuck Laura R, He Zhenzhen, Ballou Elizabeth R, Wallace Edward W J

机构信息

Institute for Cell Biology, and Centre for Engineering Biology, School of Biological Sciences, The University of Edinburgh.

MRC Centre for Medical Mycology, The University of Exeter.

出版信息

bioRxiv. 2024 Jun 11:2023.06.14.543486. doi: 10.1101/2023.06.14.543486.

Abstract

is a fungal pathogen whose virulence relies on proliferation in and dissemination to host sites, and on synthesis of a defensive yet metabolically costly polysaccharide capsule. Regulatory pathways required for virulence include a GATA-like transcription factor, Gat201, that regulates Cryptococcal virulence in both capsule-dependent and capsule-independent ways. Here we show that Gat201 is part of a negative regulatory pathway that limits fungal survival at alkaline pH. RNA-seq analysis found strong induction of expression within minutes of transfer to RPMI media at alkaline pH. Microscopy, growth curves, and colony forming unit assays show that in RPMI at alkaline pH wild-type yeast cells produce capsule but do not bud or maintain viability, while cells make buds and maintain viability, yet fail to produce capsule. is required for transcriptional upregulation of a specific set of genes, the majority of which are direct Gat201 targets. Evolutionary analysis shows that Gat201 is in a subfamily of GATA-like transcription factors that is conserved within pathogenic fungi but absent in model yeasts. This work identifies the Gat201 pathway as controlling a trade-off between proliferation and production of defensive capsule. The assays established here will allow characterisation of the mechanisms of action of the Gat201 pathway. Together, our findings urge improved understanding of the regulation of proliferation as a driver of fungal pathogenesis.

摘要

是一种真菌病原体,其毒力依赖于在宿主部位的增殖和传播,以及一种具有防御作用但代谢成本高昂的多糖荚膜的合成。毒力所需的调控途径包括一种类GATA转录因子Gat201,它以依赖荚膜和不依赖荚膜的方式调节隐球菌的毒力。在这里,我们表明Gat201是一个负调控途径的一部分,该途径限制真菌在碱性pH值下的存活。RNA测序分析发现,在转移到碱性pH值的RPMI培养基几分钟内,表达强烈诱导。显微镜检查、生长曲线和集落形成单位测定表明,在碱性pH值的RPMI中,野生型酵母细胞产生荚膜,但不发芽或维持活力,而细胞发芽并维持活力,但不产生荚膜。是一组特定基因转录上调所必需的,其中大多数是Gat201的直接靶点。进化分析表明,Gat201属于类GATA转录因子的一个亚家族,在致病真菌中保守,但在模式酵母中不存在。这项工作确定Gat201途径控制着增殖和防御性荚膜产生之间的权衡。这里建立的测定将允许对Gat201途径的作用机制进行表征。总之,我们的发现促使人们更好地理解增殖调控作为真菌发病机制的驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49d1/11181427/a52198936da0/nihpp-2023.06.14.543486v3-f0001.jpg

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