Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan Universitygrid.49470.3e, Wuhan, China.
mSphere. 2022 Dec 21;7(6):e0045022. doi: 10.1128/msphere.00450-22. Epub 2022 Nov 21.
The yeast-to-filament transition is an important cellular response to environmental stimulations in dimorphic fungi. In addition to activators, there are repressors in the cells to prevent filament formation, which is important to keep the cells in the yeast form when filamentation is not necessary. However, very few repressors of filamentation are known so far. Here, we identify a novel repressor of filamentation in the dimorphic yeast Yarrowia lipolytica, Fts2, which is a CH-type zinc finger transcription factor. We show that Δ cells exhibited increased filamentation under mild filament-inducing conditions and formed filaments under non-filament-inducing conditions. We also show that Fts2 interacts with YlSsn6, component of the Tup1-Ssn6 transcriptional corepressor, and Fts2-LexA represses a reporter in a Tup1-Ssn6-dependent manner, suggesting that Fts2 has transcriptional repressor activity and represses gene expression via Tup1-Ssn6. In addition, we show that Fts2 represses a large number of cell wall protein genes and transcription factor genes, some of which are implicated in the filamentation response. Interestingly, about two-thirds of Fts2-repressed genes are also repressed by Tup1-Ssn6, suggesting that Fts2 may repress the bulk of its target genes via Tup1-Ssn6. Lastly, we show that Fts2 expression is downregulated in response to alkaline pH and the relief of negative control by Fts2 facilitates the induction of filamentation by alkaline pH. The repressors of filamentation are important negative regulators of the yeast-to-filament transition. However, except in Candida albicans, very few repressors of filamentation are known in dimorphic fungi. More importantly, how they repress filamentation is often not clear. In this paper, we report a novel repressor of filamentation in Y. lipolytica. Fts2 is not closely related in amino acid sequence to CaNrg1 and Rfg1, two major repressors of filamentation in C. albicans, yet it represses gene expression via the transcriptional corepressor Tup1-Ssn6, similar to CaNrg1 and Rfg1. Using transcriptome sequencing, we determined the whole set of genes regulated by Fts2 and identified the major targets of Fts2 repression, which provide clues to the mechanism by which Fts2 represses filamentation. Our results have important implications for understanding the negative control of the yeast-to-filament transition in dimorphic fungi.
酵母-丝状过渡是一种重要的细胞响应环境刺激在二相真菌。除了激活剂,还有抑制剂在细胞中,以防止丝状形成,这是非常重要的保持细胞在酵母形式时,丝状是不必要的。然而,目前已知的丝状抑制剂很少。在这里,我们确定了一种新型的丝状抑制剂在二相酵母 Yarrowia lipolytica,Fts2,这是一个 CH 型锌指转录因子。我们表明,Δ细胞表现出增加丝状在温和的丝状诱导条件下,并在非丝状诱导条件下形成丝状。我们还表明,Fts2 与 YlSsn6 相互作用,Tup1-Ssn6 转录核心阻遏物的组成部分,和 Fts2-LexA 报告员依赖于 Tup1-Ssn6 ,表明 Fts2 具有转录阻遏活性,并通过 Tup1-Ssn6 抑制基因表达。此外,我们表明,Fts2 抑制大量的细胞壁蛋白基因和转录因子基因,其中一些与丝状反应有关。有趣的是,大约三分之二的 Fts2 抑制基因也受到 Tup1-Ssn6 的抑制,这表明 Fts2 可能通过 Tup1-Ssn6 抑制其大部分靶基因。最后,我们表明,Fts2 的表达下调响应碱性 pH 和负面控制的缓解 Fts2 促进了丝状的诱导碱性 pH。丝状抑制剂是酵母-丝状过渡的重要负调控因子。然而,除了 Candida albicans,在二相真菌中很少有丝状抑制剂。更重要的是,它们如何抑制丝状通常不清楚。在本文中,我们报道了一种新型丝状抑制剂在 Y. lipolytica。Fts2 在氨基酸序列上与 CaNrg1 和 Rfg1 没有密切的关系,CaNrg1 和 Rfg1 是 C. albicans 中两种主要的丝状抑制剂,但它通过转录核心阻遏物 Tup1-Ssn6 抑制基因表达,类似于 CaNrg1 和 Rfg1。使用转录组测序,我们确定了 Fts2 调节的全套基因,并确定了 Fts2 抑制的主要靶点,这为 Fts2 抑制丝状的机制提供了线索。我们的研究结果对理解二相真菌中酵母-丝状过渡的负调控具有重要意义。