含 PWWP 结构域的蛋白 Crf4-3 通过调节甾醇 C-14 去甲基化酶 ERG11 特异性地调节真菌对唑类的敏感性。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY mSphere Pub Date : 2025-01-28 Epub Date: 2024-12-13 DOI:10.1128/msphere.00703-24
Pengju Yu, Shuting Ye, Mi Zhou, Long Zhang, Zhongchi Zhang, Xianyun Sun, Shaojie Li, Chengcheng Hu
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引用次数: 0

摘要

在农业和临床环境中广泛使用的唑类抗真菌药导致了严重的耐药性。过表达唑类药物靶点14α-去甲基化酶ERG11 (CYP51)是最常见的真菌耐药机制。然而,在erg11的转录反应中是否存在其他调节蛋白尚未完全阐明。在这项研究中,我们利用已确定的控制粗神经孢子虫对唑类药物反应的erg11的关键启动子区域,通过DNA拉下实验确定了一个蛋白质Crf4-3,该蛋白含有PWWP结构域,并对唑类药物抗性发挥积极的调节作用。去除Crf4-3导致对唑类药物的敏感性提高,同时不受其他压力源的影响。此外,这种缺失导致erg11和erg6等基因对酮康唑的转录反应消失。有趣的是,erg1、erg11、erg25和erg3A的基础表达也受到crf4-3缺失的影响,表明其在固醇稳态中的作用。Crf4-3同源物广泛分布于Pezizomycotina真菌中。烟曲霉对其同源蛋白的基因缺失也显著提高了对伏立康唑等唑类药物的敏感性,主要是通过降低erg11的转录反应。我们的数据首次确定了Crf4-3是丝状真菌对唑胁迫反应的一种新的调控蛋白,为研究抗唑机制提供了新的见解。关键基因的转录控制,如erg11,是抗唑的主要驱动因素。尽管我们已经做出了相当大的努力来确定相关的转录因子,但目前我们对利用转录调控策略对抗唑类药物耐药性的了解有限。在这项研究中,我们发现含有PWWP结构域的蛋白Crf4-3,在Pezizomycotina真菌中保守,通过转录调控甾醇生物合成基因,包括erg11,来调节真菌对唑的敏感性。这些结果也拓宽了对真菌PWWP结构域蛋白在调节抗唑类抗真菌药物抗性中的作用的理解。考虑到针对人类PWWP结构域的小分子研究,Crf4-3同源物成为设计抗唑类真菌特异性药物的一个有希望的靶点。
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PWWP domain-containing protein Crf4-3 specifically modulates fungal azole susceptibility by regulating sterol C-14 demethylase ERG11.

The widespread use of azole antifungals in agriculture and clinical settings has led to serious drug resistance. Overexpression of the azole drug target 14α-demethylase ERG11 (CYP51) is the most common fungal resistance mechanism. However, the presence of additional regulatory proteins in the transcriptional response of erg11 is not yet fully elucidated. In this study, leveraging the identified key promoter region of erg11 that controls its response to azoles in Neurospora crassa, we pinpointed a protein, Crf4-3, which harbors a PWWP domain and exerts a positive regulatory influence on azole resistance, as determined by DNA pulldown assays. The removal of Crf4-3 results in heightened sensitivity to azoles while remaining unaffected by other stressors tested. Additionally, the deletion leads to the abolition of transcriptional responses of genes such as erg11 and erg6 to ketoconazole. Interestingly, the basal expression of erg1, erg11, erg25, and erg3A is also affected by the deletion of crf4-3, indicating its role in sterol homeostasis. Crf4-3 homologs are broadly distributed across the Pezizomycotina fungi. The gene deletion for its homologous protein in Aspergillus fumigatus also significantly improves sensitivity to azoles such as voriconazole, primarily through the attenuation of the transcriptional response of erg11. Our data, for the first time, identified Crf4-3 as a novel regulatory protein in the azole stress response of filamentous fungi, offering fresh insights into the mechanisms of azole resistance.IMPORTANCETranscriptional control of pivotal genes, such as erg11, stands as the primary driver of azole resistance. Although considerable effort has been dedicated to identifying transcription factors involved, our knowledge regarding the use of transcriptional regulation strategies to combat azole resistance is currently limited. In this study, we reveal that a PWWP domain-containing protein Crf4-3, which is conserved in Pezizomycotina fungi, modulates fungal azole sensitivity by transcriptionally regulating sterol biosynthetic genes, including erg11. These results also broaden the understanding of fungal PWWP domain-containing proteins regarding their roles in regulating resistance against azole antifungals. Considering research on small molecules targeting the PWWP domain in humans, Crf4-3 homolog emerges as a promising target for designing fungal-specific drugs to combat azole resistance.

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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.
期刊最新文献
Prospective comparison of the digestive tract resistome and microbiota in cattle raised in grass-fed versus grain-fed production systems. Prophages are infrequently associated with antibiotic resistance in Pseudomonas aeruginosa clinical isolates. Virus-induced perturbations in the mouse microbiome are impacted by microbial experience. Abundance of clinically relevant antimicrobial resistance genes in the golden jackal (Canis aureus) gut. Characterization of diet-linked amino acid pool influence on Fusobacterium spp. growth and metabolism.
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