Direct Regulation of tRNA and 5S rRNA Gene Transcription by Polo-like Kinase 1

被引:30
作者
Fairley, Jennifer A. [1 ,2 ]
Mitchell, Louise E. [1 ,2 ]
Berg, Tracy [1 ]
Kenneth, Niall S. [2 ]
von Schubert, Conrad [3 ]
Sillje, Herman H. W. [4 ]
Medema, Rene H. [5 ]
Nigg, Erich A. [3 ]
White, Robert J. [1 ,2 ]
机构
[1] Beatson Inst Canc Res, Glasgow G61 1BD, Lanark, Scotland
[2] Univ Glasgow, Inst Biomed & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
[3] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, NL-9700 RB Groningen, Netherlands
[5] Univ Med Ctr, Dept Med Oncol, NL-3584 CG Utrecht, Netherlands
基金
英国生物技术与生命科学研究理事会;
关键词
POLYMERASE-III TRANSCRIPTION; CELL-CYCLE REGULATION; IN-VITRO; MITOTIC REPRESSION; PLK1-DEPENDENT PHOSPHORYLATION; PROTEIN; PLK1; CHROMATIN; LOCALIZATION; CYTOKINESIS;
D O I
10.1016/j.molcel.2011.11.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Polo-like kinase Plk1 controls numerous aspects of cell-cycle progression. We show that it associates with tRNA and 5S rRNA genes and regulates their transcription by RNA polymerase Ill (pol Ill) through direct binding and phosphorylation of transcription factor Brit During interphase, Plk1 promotes tRNA and 5S rRNA expression by phosphorylating Plk1 directly on serine 450. However, this stimulatory modification is overridden at mitosis, when elevated Plk1 activity causes Bill phosphorylation on threonine 270 (T270), which prevents pol III recruitment. Thus, although Plk1 enhances net tRNA and 5S rRNA production, consistent with its proliferation-stimulating function, it also suppresses untimely transcription when cells divide. Genomic instability is apparent in cells with BM T270 mutated to alanine to resist Plk1 -directed inactivation, suggesting that chromosome segregation is vulnerable to inappropriate pol III activity.
引用
收藏
页码:541 / 552
页数:12
相关论文
共 47 条
[1]
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
[2]
Temporal Control of Contractile Ring Assembly by Plol Regulation of Myosin II Recruitment by Mid1/Anillin [J].
Almonacid, Maria ;
Celton-Morizur, Severine ;
Jakubowski, Jennifer L. ;
Dingli, Florent ;
Loew, Damarys ;
Mayeux, Adeline ;
Chen, Jun-Song ;
Gould, Kathleen L. ;
Clifford, Dawn M. ;
Paoletti, Anne .
CURRENT BIOLOGY, 2011, 21 (06) :473-479
[3]
Polo-like kinases and the orchestration of cell division [J].
Barr, FA ;
Silljé, HHW ;
Nigg, EA .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (06) :429-440
[4]
Chemical genetics reveals the requirement for Polo-like kinase 1 activity in positioning RhoA and triggering cytokinesis in human cells [J].
Burkard, Mark E. ;
Randall, Catherine L. ;
Larochelle, Stephane ;
Zhang, Chao ;
Shokat, Kevan M. ;
Fisher, Robert P. ;
Jallepalli, Prasad V. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (11) :4383-4388
[5]
p53 is a general repressor of RNA polymerase III transcription [J].
Cairns, CA ;
White, RJ .
EMBO JOURNAL, 1998, 17 (11) :3112-3123
[6]
Condensed mitotic chromatin is accessible to transcription factors and chromatin structural proteins [J].
Chen, DY ;
Dundr, M ;
Wang, C ;
Leung, A ;
Lamond, A ;
Misteli, T ;
Huang, S .
JOURNAL OF CELL BIOLOGY, 2005, 168 (01) :41-54
[7]
Cdc14 inhibits transcription by RNA polymerase I during anaphase [J].
Clemente-Blanco, Andres ;
Mayan-Santos, Maria ;
Schneider, David A. ;
Machin, Felix ;
Jarmuz, Adam ;
Tschochner, Herbert ;
Aragon, Luis .
NATURE, 2009, 458 (7235) :219-U8
[8]
Polo kinase controls cell-cycle-dependent transcription by targeting a coactivator protein [J].
Darieva, Zoulfia ;
Bulmer, Richard ;
Pic-Taylor, Aline ;
Doris, Kathryn S. ;
Geymonat, Marco ;
Sedgwick, Steven G. ;
Morgan, Brian A. ;
Sharrocks, Andrew D. .
NATURE, 2006, 444 (7118) :494-498
[9]
TFIIIB is phosphorylated, disrupted and selectively released from tRNA promoters during mitosis in vivo [J].
Fairley, JA ;
Scott, PH ;
White, RJ .
EMBO JOURNAL, 2003, 22 (21) :5841-5850
[10]
The in vitro micronucleus technique [J].
Fenech, M .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2000, 455 (1-2) :81-95