YlAaf1-YlAaf2是一种含有转录激活因子的双侧SANT结构域复合物,可促进二态酵母多脂耶氏酵母的丝状生长。

IF 3.1 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2025-09-30 Epub Date: 2025-08-18 DOI:10.1128/msphere.00403-25
Meng-Yang Xu, Zhen-Hua Wang, Xiang-Dong Gao
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引用次数: 0

摘要

酵母向丝的转变是二形真菌适应不同环境条件的重要过程。在环境刺激下激活下游靶基因的转录激活因子对这种形态转变的控制尤为重要。然而,只有有限数量的关键促动物已被确定。在这里,我们报道了YlAaf1和YlAaf2,这是一对新的含有SANT结构域的转录因子,在二态酵母中促进多脂耶氏酵母的成丝。我们发现,YlAAF1和YlAAF2的缺失和共过表达都能显著影响成丝。我们还发现YlAaf1和YlAaf2在物理上相互作用,并且两部分复合体具有转录激活活性。此外,我们发现YlAaf1和YlAaf2对碱性pH值有响应,并被YlRim101和Mhy1上调,这两个转录因子对碱诱导的丝化很重要。最后,我们发现YlAaf1-YlAaf2和Mhy1是彼此的直接调控靶点。在二形真菌中,转录因子在控制酵母向丝的转变中起着关键作用。然而,其中许多含有锌指或锌簇dna结合结构域,但不含SANT结构域,后者最初在核受体共抑制因子和许多染色质重塑复合物的亚基中被发现。在本文中,我们报道了两个新的含有SANT结构域的转录因子YlAaf1和YlAaf2,它们促进了脂性耶氏菌的丝化。YlAaf1和YlAaf2与白色念珠菌Aaf1密切相关,后者似乎也能促进丝化。YlAaf1和YlAaf2的独特之处在于它们在功能上不是简单的冗余,而是形成一个双部分转录激活子。其中一个亚基YlAaf2对环境刺激(如碱性pH)有高度反应,是酵母向细丝转变的强诱导剂。我们发现了YlAaf1-YlAaf2和Mhy1之间的串扰,Mhy1是成丝的主要调控因子。我们的研究结果提供了新的见解,以控制酵母菌到细丝的转变的调控网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
YlAaf1-YlAaf2, a bipartite SANT domain-containing complex of transcriptional activator, promotes filamentous growth in the dimorphic yeast Yarrowia lipolytica.

The yeast-to-filament transition is important for dimorphic fungi to adapt to different environmental conditions. Transcriptional activators that activate downstream target genes in response to environmental stimulations are particularly important for the control of this morphological transition. However, only a limited number of key activators of filamentation have been identified. Here, we report YlAaf1 and YlAaf2, a novel pair of SANT domain-containing transcription factors that promote filamentation in the dimorphic yeast Yarrowia lipolytica. We show that both deletion and co-overexpression of YlAAF1 and YlAAF2 affect filamentation substantially. We also show that YlAaf1 and YlAaf2 interact with each other physically, and the bipartite complex has transcriptional activation activity. In addition, we show that YlAaf1 and YlAaf2 respond to alkaline pH and are upregulated by YlRim101 and Mhy1, two key transcription factors important for alkaline-induced filamentation. Lastly, we show that YlAaf1-YlAaf2 and Mhy1 are direct regulatory targets of each other.IMPORTANCETranscription factors play critical roles in the control of the yeast-to-filament transition in dimorphic fungi. However, many of them contain zinc finger or zinc cluster DNA-binding domains, but not SANT domain, the latter of which is initially identified in nuclear receptor co-repressors and the subunits of many chromatin-remodeling complexes. In this paper, we report two novel SANT domain-containing transcription factors, YlAaf1 and YlAaf2, that promote filamentation in Yarrowia lipolytica. YlAaf1 and YlAaf2 are closely related to Candida albicans Aaf1, which also appears to promote filamentation. YlAaf1 and YlAaf2 are unique in that they are not simply redundant in function but instead form a bipartite transcriptional activator. One subunit, YlAaf2, is highly responsive to environmental stimulation such as alkaline pH, a strong inducer of the yeast-to-filament transition. We identified a crosstalk between YlAaf1-YlAaf2 and Mhy1, the master regulator of filamentation. Our results provide new insights into the regulatory networks that control the yeast-to-filament transition in Y. lipolytica.

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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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