XPB, a subunit of TFIIH, is a target of the natural product triptolide

被引:364
作者
Titov, Denis V. [1 ]
Gilman, Benjamin [2 ]
He, Qing-Li [1 ]
Bhat, Shridhar [1 ]
Low, Woon-Kai [1 ]
Dang, Yongjun [1 ]
Smeaton, Michael [3 ]
Demain, Arnold L. [4 ]
Miller, Paul S. [3 ]
Kugel, Jennifer F. [2 ]
Goodrich, James A. [2 ]
Liu, Jun O. [1 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[2] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
[3] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biochem & Mol Biol, Baltimore, MD USA
[4] Drew Univ, Charles A Dana Res Inst Scientists Emeriti, Madison, NJ 07940 USA
[5] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
关键词
RNA-POLYMERASE-II; TRANSCRIPTION FACTOR IIH; TRIPTERYGIUM-WILFORDII; COMMON TARGET; INHIBITION; PROTEIN; CYTOTOXICITY; CHEMOTHERAPY; TRANSLATION; INITIATION;
D O I
10.1038/NCHEMBIO.522
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Triptolide (1) is a structurally unique diterpene triepoxide isolated from a traditional Chinese medicinal plant with anti-inflammatory, immunosuppressive, contraceptive and antitumor activities. Its molecular mechanism of action, however, has remained largely elusive to date. We report that triptolide covalently binds to human XPB (also known as ERCC3), a subunit of the transcription factor TFIIH, and inhibits its DNA-dependent ATPase activity, which leads to the inhibition of RNA polymerase II-mediated transcription and likely nucleotide excision repair. The identification of XPB as the target of triptolide accounts for the majority of the known biological activities of triptolide. These findings also suggest that triptolide can serve as a new molecular probe for studying transcription and, potentially, as a new type of anticancer agent through inhibition of the ATPase activity of XPB.
引用
收藏
页码:182 / 188
页数:7
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