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Oncogenesis by sequestration of CBP/p300 in transcriptionally inactive hyperacetylated chromatin domains.

The EMBO journal | 2010

In a subset of poorly differentiated and highly aggressive carcinoma, a chromosomal translocation, t(15;19)(q13;p13), results in an in-frame fusion of the double bromodomain protein, BRD4, with a testis-specific protein of unknown function, NUT (nuclear protein in testis). In this study, we show that, after binding to acetylated chromatin through BRD4 bromodomains, the NUT moiety of the fusion protein strongly interacts with and recruits p300, stimulates its catalytic activity, initiating cycles of BRD4-NUT/p300 recruitment and creating transcriptionally inactive hyperacetylated chromatin domains. Using a patient-derived cell line, we show that p300 sequestration into the BRD4-NUT foci is the principal oncogenic mechanism leading to p53 inactivation. Knockdown of BRD4-NUT released p300 and restored p53-dependent regulatory mechanisms leading to cell differentiation and apoptosis. This study demonstrates how the off-context activity of a testis-specific factor could markedly alter vital cellular functions and significantly contribute to malignant cell transformation.

Pubmed ID: 20676058 RIS Download

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: 5P30CA06516-44
  • Agency: NIGMS NIH HHS, United States
    Id: R37 GM062437
  • Agency: NIGMS NIH HHS, United States
    Id: GM62437
  • Agency: NCI NIH HHS, United States
    Id: R01 CA124633
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM062437
  • Agency: NCI NIH HHS, United States
    Id: N01CO12400
  • Agency: NCI NIH HHS, United States
    Id: P30 CA006516
  • Agency: NCI NIH HHS, United States
    Id: 1R01CA124633
  • Agency: NCI NIH HHS, United States
    Id: N01-CO-12400

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RRID:SCR_002037

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