Direct Inhibition of RNA Polymerase II Transcription by RECQL5

被引:52
作者
Ayguen, Ozan [1 ]
Xu, Xiaohua [2 ]
Liu, Yilun [2 ]
Takahashi, Hidehisa [3 ]
Kong, Stephanie E. [3 ]
Conaway, Ronald C. [3 ,4 ]
Conaway, Joan W. [3 ,4 ]
Svejstrup, Jesper Q. [1 ]
机构
[1] Canc Res UK London Res Inst, Clare Hall Labs, Mech Transcript Lab, S Mimms EN6 3LD, Herts, England
[2] Yale Univ, Sch Med, Dept Therapeut Radiol, New Haven, CT 06510 USA
[3] Stowers Inst Med Res, Kansas City, MO 64110 USA
[4] Univ Kansas, Med Ctr, Dept Biochem & Mol Biol, Kansas City, KS 66160 USA
基金
美国国家卫生研究院;
关键词
ELONGATION-FACTOR; REPLICATION FORK; MEDIATOR COMPLEX; HUMAN RECQ5-BETA; SYNDROME GENE; HELICASES; RECOMBINATION; INITIATION; CHROMATIN; IMPAIRMENT;
D O I
10.1074/jbc.M109.015750
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
DNA helicases of the RECQ family are important for maintaining genome integrity, from bacteria to humans. Although progress has been made in understanding the biochemical role of some human RECQ helicases, that of RECQL5 remains elusive. We recently reported that RECQL5 interacts with RNA polymerase II (RNAPII), pointing to a role for the protein in transcription. Here, we show that RECQL5 inhibits both initiation and elongation in transcription assays reconstituted with highly purified general transcription factors and RNAPII. Such inhibition is not observed with the related, much more active RECQL1 helicase or with a version of RECQL5 that has normal helicase activity but is impaired in its ability to interact with RNAPII. Indeed, RECQL5 helicase activity is not required for inhibition. We discuss our findings in light of the fact that RECQ5(-/-) mice have elevated levels of DNA recombination and a higher incidence of cancer.
引用
收藏
页码:23197 / 23203
页数:7
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