p53-dependent expression of PIG3 during proliferation, genotoxic stress, and reversible growth arrest

被引:70
作者
Flatt, PM
Polyak, K
Tang, LJ
Scatena, CD
Westfall, MD
Rubinstein, LA
Yu, J
Kinzler, KW
Vogelstein, B
Hill, DE
Pietenpol, JA
机构
[1] Vanderbilt Univ, Sch Med, Dept Biochem, Ctr Mol Toxicol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
[3] Howard Hughes Med Inst, Baltimore, MD 21231 USA
[4] Johns Hopkins Oncol Ctr, Baltimore, MD 21231 USA
[5] Oncogene Res Prod, Cambridge, MA 02142 USA
关键词
protein; localization; p53-inducible; oxidoreductase;
D O I
10.1016/S0304-3835(00)00441-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The p53-inducible gene 3 (PIG3) was recently identified in a screen for genes induced by p53 before the onset of apoptosis. PIG3 shares significant homology with oxidoreductases from several species. In this study, PTG3-specific antibodies were used to analyze cellular PIGS protein levels under control and genotoxic stress conditions. PIG3 protein was localized to the cytoplasm and induced in primary, non-transformed, and transformed cell cultures after exposure to genotoxic agents. The induction of PIGS was p53-dependent and occurred with delayed kinetics as compared with other p53 downstream targets, such as p21 and MDM2. Using a p53-inducible cell model system, in which p53-mediated growth arrest is reversible, we found that PIG3 levels were increased during p53-mediated growth arrest. Interestingly, elevated levels of PIG3 were maintained in cells that resumed cycling in the absence of ectopic p53 expression, suggesting that PIG3 is a long-lived reporter, which may be useful for detecting transient activation of p53. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:63 / 72
页数:10
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