乙酰化
抗真菌药
组蛋白
微生物学
毒力
抗药性
组蛋白乙酰转移酶
抗真菌
表观遗传学
白色念珠菌
组蛋白乙酰转移酶
生物
DNA
白色体
遗传学
基因
作者
Shan Su,Xiuyun Li,Xinmei Yang,Yiman Li,Xueqi Chen,Shujuan Sun,Shuang Jia
标识
DOI:10.2217/fmb-2019-0343
摘要
Recently, the incidence of invasive fungal infections has significantly increased. Candida albicans (C. albicans) is the most common opportunistic fungal pathogen that infects humans. The limited number of available antifungal agents and the emergence of drug resistance pose difficulties to treatment, thus new antifungals are urgently needed. Through their functions in DNA replication, DNA repair and transcription, histone acetyltransferases (HATs) and histone deacetylases (HDACs) perform essential functions relating to growth, virulence, drug resistance and stress responses of C. albicans. Here, we summarize the physiological and pathological functions of HATs/HDACs, potential antifungal targets and underlying antifungal compounds that impact histone acetylation and deacetylation. We anticipate this review will stimulate the identification of new HAT/HDAC-related antifungal targets and antifungal agents.
科研通智能强力驱动
Strongly Powered by AbleSci AI