Histone Deacetylase 8 (HDAC8) Antibody – Rabbit Polyclonal

Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class I of the histone deacetylase family. It catalyzes the deacetylation of lysine residues in the histone N-terminal tails and represses transcription in large multiprotein complexes with transcriptional co-repressors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]

HDAC8: Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. May play a role in smooth muscle cell contractility. Belongs to the histone deacetylase family. HD type 1 subfamily. 5 isoforms of the human protein are produced by alternative splicing.

Protein type: Hydrolase; EC 3.5.1.98

Chromosomal Location of Human Ortholog: Xq13

Cellular Component: cytoplasm; cytosol; histone deacetylase complex; nuclear chromosome; nucleoplasm; nucleus; plasma membrane

Molecular Function: histone deacetylase activity; Hsp70 protein binding; Hsp90 protein binding; metal ion binding; NAD-dependent histone deacetylase activity (H3-K14 specific); protein binding; transcription factor binding

Biological Process: chromatin assembly or disassembly; chromatin modification; establishment and/or maintenance of chromatin architecture; mitotic cell cycle; negative regulation of protein ubiquitination; negative regulation of transcription from RNA polymerase II promoter; regulation of protein stability; regulation of telomere maintenance; sister chromatid cohesion; transcription, DNA-dependent

Disease: Wilson-turner X-linked Mental Retardation Syndrome