Cyclin K functions as a CDK9 regulatory subunit and participates in RNA polymerase II transcription

被引:196
作者
Fu, TJ
Peng, JM
Lee, G
Price, DH
Flores, O
机构
[1] Tularik Inc, Dept Biol, S San Francisco, CA 92080 USA
[2] Univ Iowa, Dept Biochem, Iowa City, IA 52242 USA
关键词
D O I
10.1074/jbc.274.49.34527
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
Important progress in the understanding of elongation control by RNA polymerase II (RNAPII) has come from the recent identification of the positive transcription elongation factor b (P-TEFb) and the demonstration that this factor is a protein kinase that phosphorylates the carboxyl-terminal domain (CTD) of the RNAPII largest subunit, The P-TEFb complex isolated from mammalian cells contains a catalytic subunit (CDK9), a cyclin subunit (cyclin T1 or cyclin T2), and additional, yet unidentified, polypeptides of unknown function, To identify additional factors involved in P-TEFb function we performed a yeast two-hybrid screen using CDK9 as bait and found that cyclin K interacts with CDK9 in vivo, Biochemical analyses indicate that cyclin K functions as a regulatory subunit of CDK9, The CDK9-cyclin K complex phosphorylated the CTD of RNAPII and functionally substituted for P-TEFb comprised of CDK9 and cyclin T in in vitro transcription reactions.
引用
收藏
页码:34527 / 34530
页数:4
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