Differential effects on p53-mediated cell cycle arrest vs. apoptosis by p90

被引:37
作者
Dai, Chao [1 ,2 ,3 ]
Tang, Yi [1 ,2 ]
Jung, Sung Yun [4 ,5 ]
Qin, Jun [4 ,5 ]
Aaronson, Stuart A. [6 ]
Gu, Wei [1 ,2 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Inst Canc Genet, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Pathol & Cell Biol, New York, NY 10032 USA
[3] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[4] Baylor Coll Med, Dept Biochem, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
[6] Mt Sinai Sch Med, Dept Oncol Sci, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
DNA-BINDING; TUMOR-SUPPRESSOR; P53; ACETYLATION; ACTIVATION; GENE; PUMA; AUTOPHAGY; PROMOTER; PATHWAY;
D O I
10.1073/pnas.1110988108
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
p53 functions as a central node for organizing whether the cell responds to stress with apoptosis or cell cycle arrest; however, the molecular events that lead to apoptotic responses are not completely understood. Here, we identified p90 (also called Coiled-Coil Domain Containing 8) as a unique regulator for p53. p90 has no obvious effects on either the levels of p53 or p53-mediated cell cycle arrest but is specifically required for p53-mediated apoptosis upon DNA damage. Notably, p90 is crucial for Tip60-dependent p53 acetylation at Lys120, therefore facilitating activation of the proapoptotic targets. These studies indicate that p90 is a critical cofactor for p53-mediated apoptosis through promoting Tip60-mediated p53 acetylation.
引用
收藏
页码:18937 / 18942
页数:6
相关论文
共 38 条
[1]   p53-dependent and p53-independent activation of autophagy by ARF [J].
Abida, Wassirn M. ;
Gu, Wei .
CANCER RESEARCH, 2008, 68 (02) :352-357
[2]   Acetylation of lysine 120 of p53 endows DNA-binding specificity at effective physiological salt concentration [J].
Arbely, Eyal ;
Natan, Eviatar ;
Brandt, Tobias ;
Allen, Mark D. ;
Veprintsev, Dmitry B. ;
Robinson, Carol V. ;
Chin, Jason W. ;
Joerger, Andreas C. ;
Fersht, Alan R. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (20) :8251-8256
[3]   Keeping p53 in Check: A High-Stakes Balancing Act [J].
Berger, Shelley L. .
CELL, 2010, 142 (01) :17-19
[4]   CDIP, a novel pro-apoptotic gene, regulates TNFα-mediated apoptosis in a p53-dependent manner [J].
Brown, Lauren ;
Ongusaha, Pat P. ;
Kim, Hyung-Gu ;
Nuti, Shanthy ;
Mandinova, Anna ;
Lee, Ji Won ;
Khosravi-Far, Roya ;
Aaronson, Stuart A. ;
Lee, Sam W. .
EMBO JOURNAL, 2007, 26 (14) :3410-3422
[5]   p53-Ubl fusions as models of ubiquitination, sumoylation and neddylation of p53 [J].
Carter, Stephanie ;
Vousden, Karen H. .
CELL CYCLE, 2008, 7 (16) :2519-2528
[6]   Modifications of p53: competing for the lysines [J].
Carter, Stephanie ;
Vousden, Karen H. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2009, 19 (01) :18-24
[7]   ARF-BP1/mule is a critical mediator of the ARF tumor suppressor [J].
Chen, DL ;
Kon, N ;
Li, MY ;
Zhang, WZ ;
Qin, J ;
Gu, W .
CELL, 2005, 121 (07) :1071-1083
[8]   Direct activation of Bax by p53 mediates mitochondrial membrane permeabilization and apoptosis [J].
Chipuk, JE ;
Kuwana, T ;
Bouchier-Hayes, L ;
Droin, NM ;
Newmeyer, D ;
Schuler, M ;
Green, DR .
SCIENCE, 2004, 303 (5660) :1010-1014
[9]   p53 post-translational modification: deregulated in tumorigenesis [J].
Dai, Chao ;
Gu, Wei .
TRENDS IN MOLECULAR MEDICINE, 2010, 16 (11) :528-536
[10]   P53 promoter selection - Choosing between life and death [J].
Das, Sanjeev ;
Boswell, Sarah A. ;
Aaronson, Stuart A. ;
Lee, Sam W. .
CELL CYCLE, 2008, 7 (02) :154-157