A novel p53-inducible apoptogenic gene, PRG3, encodes a homologue of the apoptosis-inducing factor (AIF)

被引:107
作者
Ohiro, Y
Garkavtsev, I
Kobayashi, S
Sreekumar, KR
Nantz, R
Higashikubo, BT
Duffy, SL
Higashikubo, R
Usheva, A
Gius, D
Kley, N
Horikoshi, N [1 ]
机构
[1] Washington Univ, Sch Med, Dept Radiat Oncol, St Louis, MO 63108 USA
[2] GPC Biotech Inc, Waltham, MA 02451 USA
[3] NCI, Radiat Oncol Sci Program, Radiat Oncol Branch, NIH, Bethesda, MD 20892 USA
[4] Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA
[5] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02129 USA
[6] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
来源
FEBS LETTERS | 2002年 / 524卷 / 1-3期
关键词
p53; target gene; cloning; apoptosis; oxidoreductase; transcription;
D O I
10.1016/S0014-5793(02)03049-1
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 induces cell cycle arrest or apoptosis in response to cellular stresses. We have identified PRG3 (p53-responsive gene 3), which is induced specifically under p53-dependent apoptotic conditions in human colon cancer cells, and encodes a novel polypeptide of 373 amino acids with a predicted molecular mass of 40.5 kDa. PRG3 has significant homology to bacterial oxidoreductases and the apoptosis-inducing factor, AIF, and the gene was assigned to chromosome 10q21.3-q22.1. Expression of PRG3 was induced by the activation of endogenous p53 and it contains a p53-responsive element. Unlike AIF, PRG3 localizes in the cytoplasm and its ectopic expression induces apoptosis. An amino-terminal deletion mutant of PRG3 that lacks a putative oxidoreductase activity retains its apoptotic activity, suggesting that the oxidoreductase activity is dispensable for the apoptotic function of PRG3. The PRG3 gene is thus a novel p53 target gene in a p53-dependent apoptosis pathway. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 171
页数:9
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