Regulation of the INK4b–ARF–INK4a tumour suppressor locus: all for one or one for all
Top Cited Papers
- 1 September 2006
- journal article
- review article
- Published by Springer Nature in Nature Reviews Molecular Cell Biology
- Vol. 7 (9) , 667-677
- https://doi.org/10.1038/nrm1987
Abstract
The INK4b-ARF-INK4a locus encodes two members of the INK4 family of cyclin-dependent kinase inhibitors, p15(INK4b) and p16(INK4a), and a completely unrelated protein, known as ARF. All three products participate in major tumour suppressor networks that are disabled in human cancer and influence key physiological processes such as replicative senescence, apoptosis and stem-cell self-renewal. Transcription from the locus is therefore kept under strict control. Mounting evidence suggests that although the individual genes can respond independently to positive and negative signals in different contexts, the entire locus might be coordinately suppressed by a cis-acting regulatory domain or by the action of Polycomb group repressor complexes.Keywords
This publication has 144 references indexed in Scilit:
- Polycomb complexes repress developmental regulators in murine embryonic stem cellsNature, 2006
- Control of Developmental Regulators by Polycomb in Human Embryonic Stem CellsCell, 2006
- A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem CellsCell, 2006
- Oncogenic activity of Cdc6 through repression of the INK4/ARF locusNature, 2006
- Contribution of p16INK4a to replicative senescence of human fibroblastsExperimental Cell Research, 2004
- The basic helix–loop–helix transcription factor TAL1/SCL inhibits the expression of the p16INK4A and pTα genesBiochemical and Biophysical Research Communications, 2003
- Comparative biology of mouse versus human cells: modelling human cancer in miceNature Reviews Cancer, 2003
- Historical claims and current interpretations of replicative agingNature Biotechnology, 2002
- Defining the molecular basis of Arf and Hdm2 interactionsJournal of Molecular Biology, 2001
- Mechanisms of cyclin-dependent kinase regulation: structures of cdks, their cyclin activators, and cip and INK4 inhibitorsJournal of Molecular Biology, 1999