p53/p63/p73 isoforms: an orchestra of isoforms to harmonise cell differentiation and response to stress

被引:417
作者
Murray-Zmijewski, F. [1 ]
Lane, D. P. [1 ]
Bourdon, J-C [1 ]
机构
[1] Univ Dundee, Dept Surg & Mol Oncol, CR UK Cell Transformat Res Grp, Ninewells Hosp, Dundee DD1 9SY, Scotland
关键词
splice; promoter; drosophila; zebrafish; development; cancer;
D O I
10.1038/sj.cdd.4401914
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
p63, p73 and p53 compose a family of transcription factors involved in cell response to stress and development. p53 is the most frequently mutated gene in cancer (50%) and loss of p53 activity is considered to be ubiquitous to all cancers. Recent publications may have a profound impact on our understanding of p53 tumour suppressor activity. p63, p73 and p53 genes have a dual gene structure conserved in drosophila, zebrafish and man. They encode for multiple p63, p73 or p53 proteins containing different protein domains (isoforms) due to multiple splicing, alternative promoter and alternative initiation of translation. In this review, we describe the different isoforms of p63, p73, p53 and their roles in development and cancer. The changes in the interactions between p53, p63 and p73 isoforms are likely to be fundamental to our understanding in the transition between normal cell cycling and the onset of tumour formation.
引用
收藏
页码:962 / 972
页数:11
相关论文
共 75 条
[1]   p53-dependent apoptosis is regulated by a C-terminally alternatively spliced form of murine p53 [J].
Almog, N ;
Goldfinger, N ;
Rotter, V .
ONCOGENE, 2000, 19 (30) :3395-3403
[2]   HIGH-FREQUENCY DEVELOPMENTAL ABNORMALITIES IN P53-DEFICIENT MICE [J].
ARMSTRONG, JF ;
KAUFMAN, MH ;
HARRISON, DJ ;
CLARKE, AR .
CURRENT BIOLOGY, 1995, 5 (08) :931-936
[3]   TP53 family members and human cancers [J].
Bénard, J ;
Douc-Rasy, S ;
Ahomadegbe, JC .
HUMAN MUTATION, 2003, 21 (03) :182-191
[4]   p53 isoforms can regulate p53 transcriptional activity [J].
Bourdon, JC ;
Fernandes, K ;
Murray-Zmijewski, F ;
Liu, G ;
Diot, A ;
Xirodimas, DP ;
Saville, MK ;
Lane, DP .
GENES & DEVELOPMENT, 2005, 19 (18) :2122-2137
[5]   Scotin, a novel p53-inducible proapoptotic protein located in the ER and the nuclear membrane [J].
Bourdon, JC ;
Renzing, J ;
Robertson, PL ;
Fernandes, KN ;
Lane, DP .
JOURNAL OF CELL BIOLOGY, 2002, 158 (02) :235-246
[6]   Further characterisation of the p53 responsive element - Identification of new candidate genes for trans-activation by p53 [J].
Bourdon, JC ;
DeguinChambon, V ;
Lelong, JC ;
Dessen, P ;
May, P ;
Debuire, B ;
May, E .
ONCOGENE, 1997, 14 (01) :85-94
[7]   Drosophila p53 binds a damage response element at the reaper locus [J].
Brodsky, MH ;
Nordstrom, W ;
Tsang, G ;
Kwan, E ;
Rubin, GM ;
Abrams, JM .
CELL, 2000, 101 (01) :103-113
[8]   Expression of ΔNp73 is a molecular marker for adverse outcome in neuroblastoma patients [J].
Casciano, I ;
Mazzocco, K ;
Boni, L ;
Pagnan, G ;
Banelli, B ;
Allemanni, G ;
Ponzoni, M ;
Tonini, GP ;
Romani, M .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (03) :246-251
[9]   Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome [J].
Celli, J ;
Duijf, P ;
Hamel, BCJ ;
Bamshad, M ;
Kramer, B ;
Smits, APT ;
Newbury-Ecob, R ;
Hennekam, RCM ;
Van Buggenhout, G ;
van Haeringen, B ;
Woods, CG ;
van Essen, AJ ;
de Waal, R ;
Vriend, G ;
Haber, DA ;
Yang, A ;
McKeon, F ;
Brunner, HG ;
van Bokhoven, H .
CELL, 1999, 99 (02) :143-153
[10]   Loss of function of def selectively up-regulates Δ113p53 expression to arrest expansion growth of digestive organs in zebrafish [J].
Chen, J ;
Ruan, H ;
Ng, SM ;
Gao, C ;
Soo, HM ;
Wu, W ;
Zhang, ZH ;
Wen, ZL ;
Lane, DP ;
Peng, JR .
GENES & DEVELOPMENT, 2005, 19 (23) :2900-2911