Histone modifications defining active genes persist after transcriptional and mitotic inactivation
- 16 December 2004
- journal article
- Published by Springer Nature in The EMBO Journal
- Vol. 24 (2), 347-357
- https://doi.org/10.1038/sj.emboj.7600516
Abstract
We examined various histone modifications across the promoter and the coding regions of constitutively active hepatic genes in G0/G1‐enriched, mitotically arrested and α‐amanitin‐blocked cells. Gene activation correlated with localized histone hyperacetylation, H3‐K4 tri‐ or dimethylation and H3‐K79 dimethylation and localized nucleosome remodeling at the promoter and the 5′ portion of the coding regions. Nucleosomes at more downstream locations were monomethylated at H3‐K4. CBP, PCAF, Brg‐1, SNF2H and FACT were recruited to the coding regions in a gene‐specific manner, in a similarly restricted promoter‐proximal pattern. Elongator, however, associated with the more downstream regions. While all factors were dissociated from the chromatin after transcriptional inactivation by α‐amanitin, the histone modifications remained stable. In mitotic cells, histone modifications on parental nucleosomes were preserved and were regenerated in a transcription‐dependent manner at the newly deposited nucleosomes, as the cells entered the next G1 phase. The findings suggest that histone modifications may function as molecular memory bookmarks for previously active locations of the genome, thus contributing to the maintenance of active chromatin states through cell division.Keywords
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