Structure, function and regulation of p63 and p73

被引:106
作者
Levrero, M
De Laurenzi, V
Costanzo, A
Gong, J
Melino, G
Wang, JYJ [1 ]
机构
[1] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Ctr Canc, La Jolla, CA 92093 USA
[3] Univ Rome La Sapienza, Fdn A Cesalpino, Rome, Italy
[4] Univ Rome Tor Vergata, Biochem Lab, IRCCS, IDI, Rome, Italy
关键词
p73; p53; c-Abl; apoptosis;
D O I
10.1038/sj.cdd.4400624
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
The p53 tumor suppressor gene is one of the most frequently mutated genes in human cancers.(1) p53 is a sequence-specific transcription factor and plays a critical role in activating the expression of genes involved in cell cycle arrest or apoptosis under conditions of genotoxic stress.(2,3) For over two decades, p53 was thought to be the only gene of its kind in the vertebrate genomes, This strong conviction, which was widely accepted in the p53 field, has now been proven to be incorrect. Two genes, referred to as p63 and p73, have been found to encode proteins that share a significant amino-acid identity in the transactivation domain, the DNA binding domain, and the oligomerization domain with p53, In the short period since their cloning, a number of investigators have reported on the structure, the function and the regulation of p63 and p73, This review summarizes the current information on the p63 and the p73 genes, with a focus on the differences between the three members in this newly defined p53-gene family.
引用
收藏
页码:1146 / 1153
页数:8
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