DNA damage-inducible gene p331NG2 negatively regulates cell proliferation through acetylation of p53

被引:181
作者
Nagashima, M
Shiseki, M
Miura, K
Hagiwara, K
Linke, SP
Pedeux, R
Wang, XW
Yokota, J
Riabowol, K
Harris, CC
机构
[1] NCI, Human Carcinogenesis Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Calgary, Hlth Sci Ctr, Dept Biochem & Mol Biol, Calgary, AB T2N 1N4, Canada
[3] Univ Calgary, Hlth Sci Ctr, Dept Oncol, Calgary, AB T2N 1N4, Canada
[4] Natl Canc Ctr, Res Inst, Div Biol, Tokyo 1040045, Japan
关键词
p33ING1; PHD-finger; apoptosis; cell cycle;
D O I
10.1073/pnas.161151798
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The p33ING1 protein is a regulator of cell cycle, senescence, and apoptosis. Three alternatively spliced transcripts of p33ING1 encode p47ING1a, p33ING1b, and p24ING1c. We cloned an additional ING family member, p33ING2/ING1L. Unlike p33ING1b, p33ING2 is induced by the DNA-damaging agents etoposide and neocarzinostatin. p33ING1b and p33ING2 negatively regulate cell growth and survival in a p53-dependent manner through induction of Gi-phase cell-cycle arrest and apoptosis. p33ING2 strongly enhances the transcriptional-transactivation activity of p53. Furthermore, p33ING2 expression increases the acetylation of p53 at Lys-382. Taken together, p33ING2 is a DNA damage-inducible gene that negatively regulates cell proliferation through activation of p53 by enhancing its acetylation.
引用
收藏
页码:9671 / 9676
页数:6
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