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PMID: 16094450 Published · ppublish English Journal Article Review

How does the histone code work?

Biochemistry and cell biology = Biochimie et biologie cellulaire ·Vol. 83 ·No. 4 ·2005-08-00 ·Pages 468-76

Cosgrove MS, Wolberger C

Abstract

Patterns of histone post-translational modifications correlate with distinct chromosomal states that regulate access to DNA, leading to the histone-code hypothesis. However, it is not clear how modification of flexible histone tails leads to changes in nucleosome dynamics and, thus, chromatin structure. The recent discovery that, like the flexible histone tails, the structured globular domain of the nucleosome core particle is also extensively modified adds a new and exciting dimension to the histone-code hypothesis, and calls for the re-examination of current models for the epigenetic regulation of chromatin structure. Here, we review these findings and other recent studies that suggest the structured globular domain of the nucleosome core particle plays a key role regulating chromatin dynamics.

MeSH Terms
Acetylation Animals Chromatin/chemistry,metabolism Histones/chemistry,physiology Humans Methylation Models, Molecular Nucleosomes/metabolism Phosphorylation Protein Processing, Post-Translational
Chemicals
Chromatin Histones Nucleosomes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cosgrove Michael S
Department of Biology, Syracuse University, NY 13244, USA. [email protected]
Wolberger Cynthia
Article Info
Journal
Biochemistry and cell biology = Biochimie et biologie cellulaire
Abbr.
Biochem Cell Biol
ISSN
0829-8211
Published
2005-08-00
Pages
468-76
Language
English
Region
Canada
NLM ID
8606068
Subset
IM
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