| Literature DB >> 12154087 |
Md Kamrul Hasan1, Tomoko Yaguchi, Takashi Sugihara, Penmetcha K R Kumar, Kazunari Taira, Roger R Reddel, Sunil C Kaul, Renu Wadhwa.
Abstract
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 p14(ARF) 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.Entities:
Mesh:
Substances:
Year: 2002 PMID: 12154087 DOI: 10.1074/jbc.M204177200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157