Yu Pengju, Ye Shuting, Zhou Mi, Zhang Long, Zhang Zhongchi, Sun Xianyun, Li Shaojie, Hu Chengcheng
Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China.
mSphere. 2025 Jan 28;10(1):e0070324. doi: 10.1128/msphere.00703-24. Epub 2024 Dec 13.
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 is not yet fully elucidated. In this study, leveraging the identified key promoter region of that controls its response to azoles in , 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 and to ketoconazole. Interestingly, the basal expression of , , , and is also affected by the deletion of , indicating its role in sterol homeostasis. Crf4-3 homologs are broadly distributed across the fungi. The gene deletion for its homologous protein in also significantly improves sensitivity to azoles such as voriconazole, primarily through the attenuation of the transcriptional response of . 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 , 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 fungi, modulates fungal azole sensitivity by transcriptionally regulating sterol biosynthetic genes, including . 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.
唑类抗真菌药物在农业和临床环境中的广泛使用已导致严重的耐药性。唑类药物靶点14α-脱甲基酶ERG11(CYP51)的过表达是最常见的真菌耐药机制。然而,在其转录反应中其他调控蛋白的存在尚未完全阐明。在本研究中,利用已确定的控制其对唑类反应的关键启动子区域,我们确定了一种蛋白质Crf4-3,其具有一个PWWP结构域,并对唑类耐药性发挥正向调控作用,这是通过DNA下拉实验确定的。去除Crf4-3会导致对唑类的敏感性增加,而对其他测试的应激源仍无影响。此外,缺失会导致诸如和等基因对酮康唑的转录反应消失。有趣的是,、、和的基础表达也受到缺失的影响,表明其在甾醇稳态中的作用。Crf4-3同源物广泛分布于真菌中。在中其同源蛋白的基因缺失也显著提高了对伏立康唑等唑类的敏感性,主要是通过减弱的转录反应。我们的数据首次确定Crf4-3是丝状真菌唑类应激反应中的一种新型调控蛋白,为唑类耐药机制提供了新的见解。重要性关键基因如的转录调控是唑类耐药的主要驱动因素。尽管已投入大量精力来鉴定涉及的转录因子,但我们目前关于使用转录调控策略来对抗唑类耐药性的知识仍然有限。在本研究中,我们揭示了一种在真菌中保守的含PWWP结构域的蛋白质Crf4-3,通过转录调控包括在内的甾醇生物合成基因来调节真菌对唑类的敏感性。这些结果也拓宽了对含真菌PWWP结构域蛋白在调节对唑类抗真菌药物耐药性方面作用的理解。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耐药性真菌特异性药物的有希望的靶点。