p53 family in development

被引:44
作者
Danilova, Nadia [1 ]
Sakamoto, Kathleen M. [2 ,3 ,4 ]
Lin, Shuo [1 ]
机构
[1] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Matel Childrens Hosp, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Jonsson Comprehens Canc Ctr, Div Hematol Oncol,Dept Pediat,Gwynne Hazen Cherry, Los Angeles, CA 90095 USA
[4] CALTECH, Div Biol, Pasadena, CA 91125 USA
关键词
p53; p63; p73; Differentiation; Proliferation; Congenital abnormalities;
D O I
10.1016/j.mod.2008.09.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The p53 family network is a unique cellular processor that integrates information from various pathways and determines cellular choices between proliferation, replication arrest/repair, differentiation, senescence, or apoptosis. The most studied role of the p53 family is the regulation of stress response and tumor suppression. By removing damaged cells from the proliferating pool, p53 family members preserve the integrity of the genome. In addition to this well recognized role, recent data implicate the p53 protein family in a broader role of controlling cell proliferation, differentiation and death. Members of the p53 protein family with opposing activity perform coordination of these processes. Imbalance of p53 protein family may contribute to a significant proportion of congenital developmental abnormalities in humans. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:919 / 931
页数:13
相关论文
共 159 条
[1]   Hedgehog signaling overrides p53-mediated tumor suppression by activating Mdm2 [J].
Abe, Yoshinori ;
Oda-Sato, Eri ;
Tobiume, Kei ;
Kawauchi, Keiko ;
Taya, Yoichi ;
Okamoto, Koji ;
Oren, Moshe ;
Tanaka, Nobuyuki .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (12) :4838-4843
[2]   Key role of p63 in BMP-4-induced epidermal commitment of embryonic stem cells [J].
Aberdam, Daniel ;
Gambaro, Karen ;
Rostagno, Philippe ;
Aberdam, Edith ;
Divonne, Stephanie de la Forest ;
Rouleau, Matthieu .
CELL CYCLE, 2007, 6 (03) :291-294
[3]  
AELDEIRY WS, 1992, NAT GENET, V1, P45
[4]   Involvement of p53 in cell differentiation and development [J].
Almog, N ;
Rotter, V .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1997, 1333 (01) :F1-F27
[5]   Identification of 315 genes essential for early zebrafish development [J].
Amsterdam, A ;
Nissen, RM ;
Sun, ZX ;
Swindell, EC ;
Farrington, S ;
Hopkins, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :12792-12797
[6]   HIGH-FREQUENCY DEVELOPMENTAL ABNORMALITIES IN P53-DEFICIENT MICE [J].
ARMSTRONG, JF ;
KAUFMAN, MH ;
HARRISON, DJ ;
CLARKE, AR .
CURRENT BIOLOGY, 1995, 5 (08) :931-936
[7]   Perturbation of rRNA synthesis in the bap28 mutation leads to apoptosis mediated by p53 in the zebrafish central nervous system [J].
Azuma, M ;
Toyama, R ;
Laver, E ;
Dawid, IB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (19) :13309-13316
[8]   Destabilization of ΔNp63α by Nedd4-mediated ubiquitination and Ubc9-mediated sumoylation, and its implications on dorsoventral patterning of the zebrafish embryo [J].
Bakkers, J ;
Camacho-Carvajal, M ;
Nowak, M ;
Kramer, C ;
Danger, B ;
Hammerschmidt, M .
CELL CYCLE, 2005, 4 (06) :790-800
[9]   Zebrafish ΔNp63 is a direct target of bmp signaling and encodes a transcriptional repressor blocking neural specification in the ventral ectoderm [J].
Bakkers, J ;
Hild, M ;
Kramer, C ;
Furutani-Seiki, M ;
Hammerschmidt, M .
DEVELOPMENTAL CELL, 2002, 2 (05) :617-627
[10]   ΔNp63α expression is regulated by the phosphoinositide 3-kinase pathway [J].
Barbieri, CE ;
Barton, CE ;
Pietenpol, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (51) :51408-51414