Cell cycle regulation and RNA polymerase II

被引:90
作者
Bregman, DB
Pestell, RG
Kidd, VJ
机构
[1] Albert Einstein Coll Med, Dept Pathol F514A, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10461 USA
[3] St Jude Childrens Res Hosp, Dept Tumor Cell Biol, Memphis, TN 38105 USA
关键词
cell cycle; RNA polymerase II; CTD; cyclin dependent kinase; Alzheimer's disease; Cockayne syndrome; checkpoints; DNA damage; p53; review;
D O I
10.2741/Bregman
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
The cell cycle and transcription by RNA polymerase II (RNAP II) are closely related. They utilize shared components. RNAP II transcriptional activity is modulated during the cell cycle. Cell cycle dependent changes in the phosphorylation status of the carboxyl-terminal domain (CTD) of the largest subunit of RNAP II (RNAP II-LS) alter transcription. Several CTD kinases are members of the cyclin-dependent kinase (cdk) superfamily, including p34(cdc2) (cdk1), cdk7, cdk8, and cdk9. Each of these cdks, with their respective cyclin partners, have been linked to cell cycle regulatory events. Other CTD kinases such as casein kinase II (CKII) and c-abl have also been implicated in cell cycle dependent modifications of the CTD. In addition, the stalling of RNAP II complexes at DNA lesions helps stimulate p53 accumulation which largely determines the cell's DNA damage response, including cell cycle arrest. Alzheimer's disease pathology results partially from activation of mitotic cdks in postmitotic neurons which can phosphorylate RNAP II-LS and other targets.
引用
收藏
页码:D244 / D257
页数:14
相关论文
共 138 条
[1]   A Ras-dependent pathway regulates RNA polymerase II phosphorylation in cardiac myocytes: Implications for cardiac hypertrophy [J].
Abdellatif, M ;
Packer, SE ;
Michael, LH ;
Zhang, D ;
Charng, MJ ;
Schneider, MD .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6729-6736
[2]   MAT1, cdk7 and cyclin H form a kinase complex which is UV light-sensitive upon association with TFIIH [J].
Adamczewski, JP ;
Rossignol, M ;
Tassan, JP ;
Nigg, EA ;
Moncollin, V ;
Egly, JM .
EMBO JOURNAL, 1996, 15 (08) :1877-1884
[3]   The p53 network [J].
Agarwal, ML ;
Taylor, WR ;
Chernov, MV ;
Chernova, OB ;
Stark, GR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :1-4
[4]   The molecular mechanism of mitotic inhibition of TFIIH is mediated by phosphorylation of CDK7 [J].
Akoulitchev, S ;
Reinberg, D .
GENES & DEVELOPMENT, 1998, 12 (22) :3541-3550
[5]  
Albert A, 1999, J CELL SCI, V112, P2493
[6]   FCP1, the RAP74-interacting subunit of a human protein phosphatase that dephosphorylates the carboxyl-terminal domain of RNA polymerase IIO [J].
Archambault, J ;
Pan, GH ;
Dahmus, GK ;
Cartier, M ;
Marshall, N ;
Zhang, S ;
Dahmus, ME ;
Greenblatt, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) :27593-27601
[7]   GENETIC-ANALYSIS OF THE REPETITIVE CARBOXYL-TERMINAL DOMAIN OF THE LARGEST SUBUNIT OF MOUSE RNA POLYMERASE-II [J].
BARTOLOMEI, MS ;
HALDEN, NF ;
CULLEN, CR ;
CORDEN, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (01) :330-339
[8]  
Baskaran R, 1996, MOL CELL BIOL, V16, P3361
[9]   Tyrosine phosphorylation of RNA polymerase II carboxyl-terminal domain by the Abl-related gene product [J].
Baskaran, R ;
Chiang, GG ;
Mysliwiec, T ;
Kruh, GD ;
Wang, JYJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) :18905-18909
[10]  
Baskaran R, 1999, CELL GROWTH DIFFER, V10, P387