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The EMBO Journal
Article . 2007 . Peer-reviewed
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The EMBO Journal
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The EMBO Journal
Article . 2007
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Bypass of senescence by the polycomb group protein CBX8 through direct binding to the INK4A-ARF locus

Authors: Dietrich, Nikolaj; Bracken, Adrian P; Trinh, Emmanuelle; Schjerling, Charlotte K; Koseki, Haruhiko; Rappsilber, Juri; Helin, Kristian; +1 Authors

Bypass of senescence by the polycomb group protein CBX8 through direct binding to the INK4A-ARF locus

Abstract

The Polycomb group (PcG) proteins are essential for embryogenesis, and their expression is often found deregulated in human cancer. The PcGs form two major protein complexes, called polycomb repressive complexes 1 and 2 (PRC1 and PRC2) whose function is to maintain transcriptional repression. Here, we demonstrate that the chromodomain-containing protein, CBX8, which is part of one of the PRC1 complexes, regulates proliferation of diploid human and mouse fibroblasts through direct binding to the INK4A-ARF locus. Furthermore, we demonstrate that CBX8 is limiting for the regulation of INK4A-ARF, and that ectopic expression of CBX8 leads to repression of the Ink4a-Arf locus and bypass of senescence, leading to cellular immortalization. Gene expression and location analysis demonstrate that besides the INK4A-ARF locus, CBX8 also regulates a number of other genes important for cell growth and survival. On the basis of these results, we conclude that CBX8 is an essential component of one of the PRC1 complexes, which directly regulate the expression of numerous target genes, including the INK4A-ARF locus, involved in cell-fate decisions.

Keywords

Polycomb Repressive Complex 1, Chromatin Immunoprecipitation, Reverse Transcriptase Polymerase Chain Reaction, Gene Expression Profiling, Nuclear Proteins, Polycomb-Group Proteins, Fibroblasts, Flow Cytometry, Mitochondrial Membrane Transport Proteins, Chromatin, Repressor Proteins, Mice, Gene Expression Regulation, Microscopy, Fluorescence, Proto-Oncogene Proteins, Animals, Humans, Cellular Senescence, Cyclin-Dependent Kinase Inhibitor p16, Cell Proliferation

  • BIP!
    Impact byBIP!
    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    174
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
174
Top 10%
Top 10%
Top 1%
gold
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