CARF is a novel protein that cooperates with mouse p19ARF (human p14ARF) in activating p53

被引:58
|
作者
Hasan, MK
Yaguchi, T
Sugihara, T
Kumar, PKR
Taira, K
Reddel, RR
Kaul, SC
Wadhwa, R
机构
[1] Natl Inst Adv Ind Sci & Technol, Res Ctr Glycosci, Tsukuba, Ibaraki 3058566, Japan
[2] Natl Inst Adv Ind Sci & Technol, Gene Funct Res Lab, Tsukuba, Ibaraki 3058566, Japan
[3] Natl Inst Adv Ind Sci & Technol, Inst Mol & Cell Biol, Tsukuba, Ibaraki 3058566, Japan
[4] Chugai Res Inst Med Sci, Ibaraki 3004101, Japan
[5] Childrens Med Res Inst, Westmead, NSW 2145, Australia
关键词
D O I
10.1074/jbc.M204177200
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 INK4a locus on chromosome 9p21 encodes two structurally distinct tumor suppressor proteins, p16(INK4a) and the alternative reading frame protein, ARF (p19(ARF) in mouse and p14(ARF) in human). Each of these proteins has a role in senescence of primary cells and activates pathways for cell cycle control and tumor suppression. The current prevailing model proposes that p19(ARF) activates p53 function by antagonizing its degradation by MDM2. It was, however, recently shown that stabilization of p53 by p14ARF occurs independent of the relocalization of MDM2 to the nucleolus. We have identified a novel collaborator of ARF, CARF. It co-localizes and interacts with ARF in the nucleolus. We demonstrate that CARF is co-regulated with ARF, cooperates with it in activating p53, and thus acts as a novel component of the ARF-p53-p21 pathway.
引用
收藏
页码:37765 / 37770
页数:6
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