4.7 Article

p16INK4a-mediated suppression of telomerase in normal and malignant human breast cells

Journal

AGING CELL
Volume 9, Issue 5, Pages 736-746

Publisher

WILEY
DOI: 10.1111/j.1474-9726.2010.00599.x

Keywords

heterochromatin; histone methylation; hTERT; INK4a; senescence

Funding

  1. Flight Attendant Medical Research Institute [032122]
  2. Komen for the Cure Research Grant [BCTR0707231]
  3. National Institutes of Health [AG09909, AG17242]
  4. Office of Energy Research, Office of Health and Biological Research, US Department of Energy [DE-AC03-76SF00098]
  5. Komen for the Cure Postdoctoral Fellowship [0707408]

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P>The cyclin-dependent kinase inhibitor p16INK4a (CDKN2A) is an important tumor suppressor gene frequently inactivated in human tumors. p16 suppresses the development of cancer by triggering an irreversible arrest of cell proliferation termed cellular senescence. Here, we describe another anti-oncogenic function of p16 in addition to its ability to halt cell cycle progression. We show that transient expression of p16 stably represses the hTERT gene, encoding the catalytic subunit of telomerase, in both normal and malignant breast epithelial cells. Short-term p16 expression increases the amount of histone H3 trimethylated on lysine 27 (H3K27) bound to the hTERT promoter, resulting in transcriptional silencing, likely mediated by polycomb complexes. Our results indicate that transient p16 exposure may prevent malignant progression in dividing cells by irreversible repression of genes, such as hTERT, whose activity is necessary for extensive self-renewal.

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