Puma is an essential mediator of p53-dependent and -independent apoptotic pathways

被引:902
作者
Jeffers, JR
Parganas, E
Lee, Y
Yang, CY
Wang, JL
Brennan, J
MacLean, KH
Han, JW
Chittenden, T
Ihle, JN
McKinnon, PJ
Cleveland, JL
Zambetti, GP
机构
[1] St Jude Childrens Res Hosp, Memphis, TN 38105 USA
[2] Howard Hughes Med Inst, Memphis, TN 38105 USA
[3] ImmunoGen Inc, Cambridge, MA 02139 USA
关键词
D O I
10.1016/S1535-6108(03)00244-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Puma encodes a BH3-only protein that is induced by the p53 tumor suppressor and other apoptotic stimuli. To assess its physiological role in apoptosis, we generated Puma knockout mice by gene targeting. Here we report that Puma is essential for hematopoietic cell death triggered by ionizing radiation (IR), deregulated c-Myc expression, and cytokine withdrawal. Puma is also required for IR-induced death throughout the developing nervous system and accounts for nearly all of the apoptotic activity attributed to p53 under these conditions. These findings establish Puma as a principal mediator of cell death in response to diverse apoptotic signals, implicating Puma as a likely tumor suppressor.
引用
收藏
页码:321 / 328
页数:8
相关论文
共 25 条
[1]
Proapoptotic Bcl-2 relative bim required for certain apoptotic responses, leukocyte homeostasis, and to preclude autoimmunity [J].
Bouillet, P ;
Metcalf, D ;
Huang, DCS ;
Tarlinton, DM ;
Kay, TWH ;
Köntgen, F ;
Adams, JM ;
Strasser, A .
SCIENCE, 1999, 286 (5445) :1735-1738
[2]
Atm and Bax cooperate in ionizing radiation-induced apoptosis in the central nervous system [J].
Chong, MJ ;
Murray, MR ;
Gosink, EC ;
Russell, HRC ;
Srinivasan, A ;
Kapsetaki, M ;
Korsmeyer, SJ ;
McKinnon, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (02) :889-894
[3]
THYMOCYTE APOPTOSIS INDUCED BY P53-DEPENDENT AND INDEPENDENT PATHWAYS [J].
CLARKE, AR ;
PURDIE, CA ;
HARRISON, DJ ;
MORRIS, RG ;
BIRD, CC ;
HOOPER, ML ;
WYLLIE, AH .
NATURE, 1993, 362 (6423) :849-852
[4]
MICE LACKING P21(C/P1/WAF1) UNDERGO NORMAL DEVELOPMENT, BUT ARE DEFECTIVE IN G1 CHECKPOINT CONTROL [J].
DENG, CX ;
ZHANG, PM ;
HARPER, JW ;
ELLEDGE, SJ ;
LEDER, P .
CELL, 1995, 82 (04) :675-684
[5]
The codon 72 polymorphic variants of p53 have markedly different apoptotic potential [J].
Dumont, P ;
Leu, JIJ ;
Della Pietra, AC ;
George, DL ;
Murphy, M .
NATURE GENETICS, 2003, 33 (03) :357-365
[6]
Disruption of the ARF-Mdm2-p53 tumor suppressor pathway in Myc-induced lymphomagenesis [J].
Eischen, CM ;
Weber, JD ;
Roussel, MF ;
Sherr, CJ ;
Cleveland, JL .
GENES & DEVELOPMENT, 1999, 13 (20) :2658-2669
[7]
EISHCEN CM, 2001, MOL CELL BIOL, V21, P5063
[8]
Expression of bbc3, a pro-apoptotic BH3-only gene, is regulated by diverse cell death and survival signals [J].
Han, JW ;
Flemington, C ;
Houghton, AB ;
Gu, ZM ;
Zambetti, GP ;
Lutz, RJ ;
Zhu, L ;
Chittenden, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (20) :11318-11323
[9]
Requirement for Atm in ionizing radiation-induced cell death in the developing central nervous system [J].
Herzog, KH ;
Chong, MJ ;
Kapsetaki, M ;
Morgan, JI ;
McKinnon, PJ .
SCIENCE, 1998, 280 (5366) :1089-1091
[10]
BAX-DEFICIENT MICE WITH LYMPHOID HYPERPLASIA AND MALE GERM-CELL DEATH [J].
KNUDSON, CM ;
TUNG, KSK ;
TOURTELLOTTE, WG ;
BROWN, GAJ ;
KORSMEYER, SJ .
SCIENCE, 1995, 270 (5233) :96-99