| Literature DB >> 22077150 |
Elizabeth W Bradley1, Meghan E McGee-Lawrence, Jennifer J Westendorf.
Abstract
Histone deacetylases (Hdacs) remove acetyl groups (CH3CO-) from ε-amino groups in lysine residues within histones and other proteins. This posttranslational (de) modification alters protein stability, protein-protein interactions, and chromatin structure. Hdac activity plays important roles in the development of all organs and tissues, including the mineralized skeleton. Bone is a dynamic tissue that forms and regenerates by two processes: endochondral and intramembranous ossification. Chondrocytes and osteoblasts are responsible for producing the extracellular matrices of skeletal tissues. Several Hdacs contribute to the molecular pathways and chromatin changes that regulate tissue-specific gene expression during chondrocyte and osteoblast specification, maturation, and terminal differentiation. In this review, we summarize the roles of class I and class II Hdacs in chondrocytes and osteoblasts. The effects of small molecule Hdac inhibitors on the skeleton are also discussed.Entities:
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Year: 2011 PMID: 22077150 PMCID: PMC3218555 DOI: 10.1615/critreveukargeneexpr.v21.i2.10
Source DB: PubMed Journal: Crit Rev Eukaryot Gene Expr ISSN: 1045-4403 Impact factor: 1.807