Inhibiting eukaryotic transcription Which compound to choose? How to evaluate its activity?

被引:418
作者
Bensaude, Olivier [1 ]
机构
[1] IBENS, UMR CNRS 8197, UA INSERM 1024, Paris, France
来源
TRANSCRIPTION-AUSTIN | 2011年 / 2卷 / 03期
关键词
RNA polyrnerase; transcription; amanitin; actinomycin; DRB; flavopiridol; triptolide; CDK9; TFIIH; Rpb1;
D O I
10.4161/trns.2.3.16172
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
This review first discusses ways in which we can evaluate transcription inhibition, describe changes in nuclear structure due to transcription inhibition, and report on genes that are paradoxically stimulated by transcription inhibition. Next, it summarizes the characteristics and mechanisms of commonly used inhibitors: alpha-amanitin is highly selective for RNAP II and RNAP III but its action is slow, actinotriycin D is fast but its selectivity is poor, CDK9 inhibitors such as DRB and fiavopiridol are fast and reversible but many genes escape transcription inhibition. New compounds, such as triptolide, are fast and selective and able to completely arrest transcription by triggering rapid degradation of RNAP II.
引用
收藏
页码:103 / 108
页数:6
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