Histone deacetylases (Hdacs) remove acetyl groups (CH3CO-) from e-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.
|Original language||English (US)|
|Number of pages||13|
|Journal||Critical Reviews in Eukaryotic Gene Expression|
|State||Published - Nov 14 2011|
- Lysine deacetylase
ASJC Scopus subject areas
- Molecular Biology