A natural product targets BRD4 to inhibit phase separation and gene transcription

被引:12
|
作者
Wang, Cong [1 ,2 ]
Lu, Huasong [2 ,3 ]
Liu, Xiangzhong [1 ]
Gao, Xiang [1 ]
Tian, Wenjing [1 ]
Chen, Haifeng [1 ]
Xue, Yuhua [1 ]
Zhou, Qiang [2 ]
机构
[1] Xiamen Univ, Sch Pharmaceut Sci, State Key Lab Cellular Stress Biol, Fujian Prov Key Lab Innovat Drug Target Res, Xiangan South Rd, Xiamen 361102, Fujian, Peoples R China
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[3] Zhejiang Univ, Life Sci Inst, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划; 美国国家卫生研究院;
关键词
BET BROMODOMAIN INHIBITION; P-TEFB; SELECTIVE-INHIBITION; HIV LATENCY; ELONGATION; MYC;
D O I
10.1016/j.isci.2021.103719
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The BET-bromodomain protein BRD4 uses two bromodomains to target acetyl-histones and other domains to recruit P-TEFb and other transcription factors to stimulate transcription of proto-oncogenes and key cell identity genes. Recent studies show that its ability to form phase-separated condensates that cluster preferentially at the super-enhancer regions of target genes is key for BRD4 to exert its functions. Here, we describe the identification of a natural product called PCG from polygonum cuspidatum Sieb.et Zucc., a traditional Chinese medicinal herb, that directly binds to BRD4. This binding inhibits BRD4 phase separation, turns dynamic BRD4 nuclear condensates into static aggregates, and effectively shuts down transcription of BRD4-dependent genes. Thus, through PCG we have discovered a BET inhibitor that not only selectively targets BRD4 but also works by suppressing phase separation, a mechanism of action that is different from those of the other known BET inhibitors.
引用
收藏
页数:17
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