Transcriptional regulation by p53: one protein, many possibilities

被引:415
作者
Laptenko, O. [1 ]
Prives, C. [1 ]
机构
[1] Columbia Univ, Dept Sci Biol, New York, NY 10027 USA
关键词
p53; transcriptional activation/suppression; functional domain; co-activator;
D O I
10.1038/sj.cdd.4401916
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 protein is a DNA sequence-specific transcriptional regulator that, in response to various forms of cellular stress, controls the expression of numerous genes involved in cellular outcomes including among others, cell cycle arrest and cell death. Two key features of the p53 protein are required for its transcriptional activities: its ability to recognize and bind specific DNA sequences and to recruit both general and specialized transcriptional co-regulators. In fact, multiple interactions with co-activators and co-repressors as well as with the components of the general transcriptional machinery allow p53 to either promote or inhibit transcription of different target genes. This review focuses on some of the salient features of the interactions of p53 with DNA and with factors that regulate transcription. We discuss as well the complexities of the functional domains of p53 with respect to these interactions.
引用
收藏
页码:951 / 961
页数:11
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共 143 条
  • [21] Structure, function, and aggregation of the zinc-free form of the p53 DNA binding domain
    Butler, JS
    Loh, SN
    [J]. BIOCHEMISTRY, 2003, 42 (08) : 2396 - 2403
  • [22] p53 is a general repressor of RNA polymerase III transcription
    Cairns, CA
    White, RJ
    [J]. EMBO JOURNAL, 1998, 17 (11) : 3112 - 3123
  • [23] Two tandem and independent sub-activation domains in the amino terminus of p53 require the adaptor complex for activity
    Candau, R
    Scolnick, DM
    Darpino, P
    Ying, CY
    Halazonetis, TD
    Berger, SL
    [J]. ONCOGENE, 1997, 15 (07) : 807 - 816
  • [24] How many mutant p53 molecules are needed to inactivate a tetramer?
    Chan, WM
    Siu, WY
    Lau, A
    Poon, RYC
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (08) : 3536 - 3551
  • [25] TRANSACTIVATION ABILITY OF P53 TRANSCRIPTIONAL ACTIVATION DOMAIN IS DIRECTLY RELATED TO THE BINDING-AFFINITY TO TATA-BINDING PROTEIN
    CHANG, J
    KIM, DH
    LEE, SW
    CHOI, KY
    SUNG, YC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) : 25014 - 25019
  • [26] Phosphorylation of Ser-20 mediates stabilization of human p53 in response to DNA damage
    Chehab, NH
    Malikzay, A
    Stavridi, ES
    Halazonetis, TD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) : 13777 - 13782
  • [27] CRYSTAL-STRUCTURE OF A P53 TUMOR-SUPPRESSOR DNA COMPLEX - UNDERSTANDING TUMORIGENIC MUTATIONS
    CHO, YJ
    GORINA, S
    JEFFREY, PD
    PAVLETICH, NP
    [J]. SCIENCE, 1994, 265 (5170) : 346 - 355
  • [28] Regulation of p53 activity through lysine methylation
    Chuikov, S
    Kurash, JK
    Wilson, JR
    Xiao, B
    Justin, N
    Ivanov, GS
    McKinney, K
    Tempst, P
    Prives, C
    Gamblin, SJ
    Barlev, NA
    Reinberg, D
    [J]. NATURE, 2004, 432 (7015) : 353 - 360
  • [29] Transcriptional regulation of mitotic checkpoint gene MAD1 by p53
    Chun, ACS
    Jin, DY
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (39) : 37439 - 37450
  • [30] A polymorphic microsatellite that mediates induction of PIG3 by p53
    Contente, A
    Dittmer, A
    Koch, MC
    Roth, J
    Dobbelstein, M
    [J]. NATURE GENETICS, 2002, 30 (03) : 315 - 320