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Cell cycle‐dependent recruitment of HDAC‐1 correlates with deacetylation of histone H4 on an Rb–E2F target promoter
Author(s) -
Ferreira Roger,
Naguibneva Irina,
Mathieu Marion,
AitSiAli Slimane,
Robin Philippe,
Pritchard Linda L,
HarelBellan Annick
Publication year - 2001
Publication title -
embo reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.584
H-Index - 184
eISSN - 1469-3178
pISSN - 1469-221X
DOI - 10.1093/embo-reports/kve173
Subject(s) - histone h4 , acetylation , e2f , histone deacetylase , histone , histone deacetylase 5 , chromatin immunoprecipitation , hdac8 , chromatin , hdac11 , hdac4 , microbiology and biotechnology , biology , chemistry , promoter , cell cycle , cell , biochemistry , gene expression , dna , gene
The transcription factor E2F, which is a key element in the control of cell proliferation, is repressed by Rb and other pocket proteins in growth‐arrested differentiating cells, as well as in proliferating cells when they progress through early G 1 . It is not known whether similar mechanisms are operative in the two situations. A body of data suggests that E2F repression by pocket proteins involves class I histone deacetylases (HDACs). It has been hypothesized that these enzymes are recruited to E2F target promoters where they deacetylate histones. Here we have tested this hypothesis directly by using formaldehyde cross‐linked chromatin immunoprecipitation (XChIP) assays to evaluate HDAC association in living cells. Our data show that a histone deacetylase, HDAC‐1, is stably bound to an E2F target promoter during early G 1 in proliferating cells and released at the G 1 –S transition. In addition, our results reveal an inverse correlation between HDAC‐1 recruitment and histone H4 acetylation on specific lysines.