Chemical inhibition of the TFIIH-associated kinase Cdk7/Kin28 does not impair global mRNA synthesis

被引:94
作者
Kanin, Elenita I.
Kipp, Ryan T.
Kung, Charles
Slattery, Matthew
Viale, Agnes
Hahn, Steven
Shokat, Kevan M.
Ansari, Aseem Z.
机构
[1] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[2] Univ Wisconsin, Genome Ctr Wisconsin, Madison, WI 53706 USA
[3] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[4] Univ Wisconsin, Sch Pharm, Madison, WI 53705 USA
[5] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[6] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
关键词
chemical genetics; CTD kinase; TFIIH disassembly; CARBOXY-TERMINAL DOMAIN; POLYMERASE-II TRANSCRIPTION; CYCLIN-DEPENDENT KINASES; CDK-ACTIVATING KINASE; SACCHAROMYCES-CEREVISIAE; MEDIATED TRANSCRIPTION; ENVIRONMENTAL-CHANGES; PROMOTER ESCAPE; GENE-EXPRESSION; CAPPING ENZYME;
D O I
10.1073/pnas.0611505104
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 process of gene transcription requires the recruitment of a hypophosphorylated form of RNA polymerase II (Pol II) to a gene promoter. The TFIIH-associated kinase Cdk7/Kin28 hyperphosphorylates the promoter-bound polymerase; this event is thought to play a crucial role in transcription initiation and promoter clearance. Studies using temperature-sensitive mutants of Kin28 have provided the most compelling evidence for an essential role of its kinase activity in global mRNA synthesis. In contrast, using a small molecule inhibitor that specifically inhibits Kin28 in vivo, we find that the kinase activity is not essential for global transcription. Unlike the temperature-sensitive alleles, the small-molecule inhibitor does not perturb protein-protein interactions nor does it provoke the disassociation of TFIIH from gene promoters. These results lead us to conclude that other functions of TFIIH, rather than the kinase activity, are critical for global gene transcription.
引用
收藏
页码:5812 / 5817
页数:6
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