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利用一种新的数据资源来定义[具体生物名称]对环境信号的反应:宿主样信号如何驱动[具体生物名称]中的基因表达和荚膜扩张。

Leveraging a new data resource to define the response of to environmental signals: How host-like signals drive gene expression and capsule expansion in .

作者信息

Kang Yu Sung, Jung Jeffery, Brown Holly, Mateusiak Chase, Doering Tamara L, Brent Michael R

机构信息

These authors contributed equally.

Center for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

bioRxiv. 2024 Oct 24:2023.04.19.537239. doi: 10.1101/2023.04.19.537239.

Abstract

is an opportunistic fungal pathogen with a polysaccharide capsule that becomes greatly enlarged in the mammalian host and during growth under host-like conditions. To understand how individual environmental signals affect capsule size and gene expression, we grew cells in all combinations of five signals implicated in capsule size and systematically measured cell and capsule sizes. We also sampled these cultures over time and performed RNA-Seq in quadruplicate, yielding 881 RNA-Seq samples. Analysis of the resulting data sets showed that capsule induction in tissue culture medium, typically used to represent host-like conditions, requires the presence of either CO or exogenous cyclic AMP (cAMP). Surprisingly, adding either of these pushes overall gene expression in the opposite direction from tissue culture media alone, even though both are required for capsule development. Another unexpected finding was that rich medium blocks capsule growth completely. Statistical analysis further revealed many genes whose expression is associated with capsule thickness; deletion of one of these significantly reduced capsule size. Beyond illuminating capsule induction, our massive, uniformly collected dataset will be a significant resource for the research community.

摘要

是一种机会性真菌病原体,具有多糖荚膜,在哺乳动物宿主中以及在类似宿主条件下生长时会大大增大。为了了解单个环境信号如何影响荚膜大小和基因表达,我们在与荚膜大小相关的五个信号的所有组合中培养细胞,并系统地测量细胞和荚膜大小。我们还随时间对这些培养物进行采样,并进行了四次重复的RNA测序,产生了881个RNA测序样本。对所得数据集的分析表明,通常用于代表类似宿主条件的组织培养基中的荚膜诱导需要存在CO或外源性环磷酸腺苷(cAMP)。令人惊讶的是,添加这两者中的任何一种都会使整体基因表达朝着与单独使用组织培养基相反的方向发展,尽管两者都是荚膜发育所必需的。另一个意外发现是丰富培养基会完全阻止荚膜生长。统计分析进一步揭示了许多其表达与荚膜厚度相关的基因;删除其中一个会显著减小荚膜大小。除了阐明荚膜诱导外,我们大量、统一收集的数据集将成为研究界的重要资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b03/11528482/08971fa7209f/nihpp-2023.04.19.537239v3-f0001.jpg

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