揭示StuA在红毛藓转录调控中的作用:从全局调控动力学到ph响应程序控制。

IF 3.6 3区 生物学 Q2 MYCOLOGY
Leonardo Martins-Santana, Monise Fazolin Petrucelli, Pablo R Sanches, Nilce M Martinez-Rossi, Antonio Rossi
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引用次数: 0

摘要

红毛癣是一种皮肤病的主要病原体。为了建立感染,这种真菌协调了许多与生化过程、生理适应和转录网络相关的机制。转录因子(tf)是当红绒t与角质化组织相互作用并促进防御反应以防止真菌定植时引发生物反应的主要蛋白质。在这项研究中,我们研究了TF StuA(一种最近发现的红毛霉蛋白)在控制真菌对葡萄糖和角蛋白的转录程序中的作用。该方法基于RNA测序数据,揭示了至少33个TF基因在葡萄糖或角蛋白中差异表达。我们还发现,StuA调节pH信号转录因子PacC, PacC是一种相关的TF,用于红绒t的角蛋白同化。此外,我们证明了StuA正向调节pacC,并影响角蛋白培养中pacC转录本的选择性剪接事件。我们的研究结果表明,在与角化细胞共培养中,StuA抑制pacC转录并调节pal通路基因的表达,此外还表明StuA在宿主的pH识别反应和营养吸收中起关键作用。作为后续研究,我们的结果揭示了发现治疗皮肤真菌病的新靶点,并阐明了红毛霉发病机制的基础转录网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unveiling the Role of StuA in Transcription Regulation in Trichophyton rubrum: From Global Regulation Dynamics to the pH-Responsive Program Control.

The dermatophyte Trichophyton rubrum is the primary causative agent of a cutaneous disease known as dermatophytosis. To establish an infection, this fungus coordinates many mechanisms related to biochemical processes, physiological adaptation, and transcriptional networks. Transcription factors (TFs) are the main proteins that elicit biological responses when T. rubrum interacts with keratinized tissues and promotes defense responses to prevent fungal colonization. In this study, we investigated the role of the TF StuA, a recently described T. rubrum protein, in controlling this fungal transcriptional program in response to glucose and keratin. This approach, based on RNA sequencing data, revealed at least 33 TF genes differentially expressed in glucose or keratin. We also showed that StuA regulates the pH signaling transcription factor, PacC, a relevant TF recruited for keratin assimilation in T. rubrum. Furthermore, we demonstrated that StuA modulates positively pacC and influences alternative splicing events of pacC transcripts in keratin cultures. Our findings revealed that StuA represses pacC transcription in a co-culture with keratinocytes and modulates the expression of the pal pathway genes, besides suggesting that StuA is pivotal for pH recognition responses and nutrient assimilation in the host. As a follow-up study, our results shed light on discovering new targets to treat dermatophytosis and elucidating transcriptional networks that are fundamental to T. rubrum pathogenesis.

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来源期刊
Mycopathologia
Mycopathologia 生物-真菌学
CiteScore
6.80
自引率
3.60%
发文量
76
审稿时长
3 months
期刊介绍: Mycopathologia is an official journal of the International Union of Microbiological Societies (IUMS). Mycopathologia was founded in 1938 with the mission to ‘diffuse the understanding of fungal diseases in man and animals among mycologists’. Many of the milestones discoveries in the field of medical mycology have been communicated through the pages of this journal. Mycopathologia covers a diverse, interdisciplinary range of topics that is unique in breadth and depth. The journal publishes peer-reviewed, original articles highlighting important developments concerning medically important fungi and fungal diseases. The journal highlights important developments in fungal systematics and taxonomy, laboratory diagnosis of fungal infections, antifungal drugs, clinical presentation and treatment, and epidemiology of fungal diseases globally. Timely opinion articles, mini-reviews, and other communications are usually invited at the discretion of the editorial board. Unique case reports highlighting unprecedented progress in the diagnosis and treatment of fungal infections, are published in every issue of the journal. MycopathologiaIMAGE is another regular feature for a brief clinical report of potential interest to a mixed audience of physicians and laboratory scientists. MycopathologiaGENOME is designed for the rapid publication of new genomes of human and animal pathogenic fungi using a checklist-based, standardized format.
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