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Mol Cell ; 38(4): 539-50, 2010 May 28.
Artigo em Inglês | MEDLINE | ID: mdl-20513429

RESUMO

The p14/p19(ARF) (ARF) product of the CDKN2A gene displays tumor suppressor activity both in the presence and absence of p53/TP53. In p53-negative cells, ARF arrests cell proliferation, at least in part, by suppressing ribosomal RNA synthesis. We show that ARF does this by controlling the subnuclear localization of the RNA polymerase I transcription termination factor, TTF-I. TTF-I shuttles between nucleoplasm and nucleolus with the aid of the chaperone NPM/B23 and a nucleolar localization sequence within its N-terminal regulatory domain. ARF inhibits nucleolar import of TTF-I by binding to this nucleolar localization sequence, causing the accumulation of TTF-I in the nucleoplasm. Depletion of TTF-I recapitulates the effects of ARF on ribosomal RNA synthesis and is rescued by the introduction of a TTF-I transgene. Thus, our data delineate the pathway by which ARF regulates ribosomal RNA synthesis and provide a compelling explanation for the role of NPM.


Assuntos
Proteínas de Ligação a DNA/metabolismo , RNA Polimerase I/metabolismo , Ribossomos/metabolismo , Proteína Supressora de Tumor p14ARF/metabolismo , Animais , Linhagem Celular , Células HeLa , Humanos , Camundongos , Camundongos Endogâmicos C57BL , Células NIH 3T3 , Fatores de Transcrição
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