Bone Reports (Dec 2017)

Histone deacetylases and their roles in mineralized tissue regeneration

  • Nam Cong-Nhat Huynh,
  • Vincent Everts,
  • Ruchanee Salingcarnboriboon Ampornaramveth

DOI
https://doi.org/10.1016/j.bonr.2017.08.001
Journal volume & issue
Vol. 7, no. C
pp. 33 – 40

Abstract

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Histone acetylation is an important epigenetic mechanism that controls expression of certain genes. It includes non-sequence-based changes of chromosomal regional structure that can alter the expression of genes. Acetylation of histones is controlled by the activity of two groups of enzymes: the histone acetyltransferases (HATs) and histone deacetylases (HDACs). HDACs remove acetyl groups from the histone tail, which alters its charge and thus promotes compaction of DNA in the nucleosome. HDACs render the chromatin structure into a more compact form of heterochromatin, which makes the genes inaccessible for transcription. By altering the transcriptional activity of bone-associated genes, HDACs control both osteogenesis and osteoclastogenesis. This review presents an overview of the function of HDACs in the modulation of bone formation. Special attention is paid to the use of HDAC inhibitors in mineralized tissue regeneration from cells of dental origin.

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