在新生隐球菌中,宿主样信号如何驱动基因表达和基因表达如何驱动包膜扩张。

Yu Sung Kang, Jeffery Jung, Holly Brown, Chase Mateusiak, Tamara L Doering, Michael R Brent
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引用次数: 0

摘要

新生隐球菌是一种具有多糖包膜的机会性真菌病原体,在哺乳动物宿主中和体外生长过程中,多糖包膜会因宿主样条件而大大增大。为了了解单个宿主样信号如何影响包膜大小和基因表达,我们在有和没有怀疑影响包膜大小的5种信号的所有组合的情况下培养细胞,并系统测量了47458个细胞的细胞和包膜大小。我们还收集了30、90、180和1440分钟的RNA-Seq样本,并进行了一式四份的RNA-Seq,得到881个RNA-Seqs样本。这个庞大、统一收集的数据集将成为研究界的重要资源。分析表明,胶囊诱导需要组织培养基和CO2或外源性环状AMP(第二信使)。富培养基(YPD)完全阻断胶囊生长,DMEM允许,RPMI产生最大的胶囊。培养基对整体基因表达的影响最大,其次是二氧化碳、哺乳动物体温(37°比30°),然后是cAMP。令人惊讶的是,添加CO2或cAMP将整个基因表达推向与组织培养基相反的方向,即使组织培养基和CO2或cAMP都是胶囊发育所必需的。通过模拟基因表达和胶囊大小之间的关系,我们确定了缺失会影响胶囊大小的新基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Leveraging a new data resource to define the response of <i>C. neoformans</i> to environmental signals: How host-like signals drive gene expression and capsule expansion in <i>Cryptococcus neoformans</i>.

Leveraging a new data resource to define the response of <i>C. neoformans</i> to environmental signals: How host-like signals drive gene expression and capsule expansion in <i>Cryptococcus neoformans</i>.

Leveraging a new data resource to define the response of <i>C. neoformans</i> to environmental signals: How host-like signals drive gene expression and capsule expansion in <i>Cryptococcus neoformans</i>.

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

Cryptococcus neoformans is an opportunistic fungal pathogen with a polysaccharide capsule that becomes greatly enlarged in the mammalian host and during in vitro 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 CO2 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.

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