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Ink and Arf

Jonathan B Weitzman

Genome Biology 2001, 2:spotlight-20010807-02  doi:10.1186/gb-spotlight-20010807-02

The electronic version of this article is the complete one and can be found online at:

Published:7 August 2001

© 2001 BioMed Central Ltd

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When primary murine fibroblasts are placed in culture they exhibit replicative senescence, associated with the induction of cell-cycle inhibitors. The Ink4a-Arf locus encodes two proteins, p16Ink4a and p19Arf, which regulate the cell cycle by modulating the activities of pRb and p53, respectively. In the Early Edition of the Proceedings of the National Academy of Sciences, Randle et al. describe the role of p19Arf in preventing immortalization of bone-marrow-derived preB cells and macrophages (Proc Natl Acad Sci USA, 10.1073/pnas.171217498). PreB cells from Arf-null mice evaded the senescence observed in wild-type cells and continued to express high levels of p16Ink4a. But Arf-null macrophages lost p16Ink4a during the immortalization process, by methylation-suppression of the Ink4a promoter. Wild-type macrophages also lost p16Ink4a expression in established lines. The authors conclude that loss of the two Ink4a-Arf transcripts has different effects on senescence of preB cells or macrophages.


  1. Cellular senescence as a tumor-protection mechanism: the essential role of counting

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  2. Alternative reading frames of the INK4a tumor suppressor gene encode two unrelated proteins capable of inducing cell cycle arrest

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  3. [] webcite

    Proceedings of the National Academy of Sciences

  4. [] webcite

    Differential effects of p19Arf and p16Ink4a loss on senescence of murine bone marrow-derived preB cells and macrophages