| Literature DB >> 15992689 |
Nagarama Kothapalli1, Gabriela Camporeale, Alice Kueh, Yap C Chew, Anna M Oommen, Jacob B Griffin, Janos Zempleni.
Abstract
Histones H1, H2A, H2B, H3 and H4 are DNA-binding proteins that mediate the folding of DNA into chromatin. Various posttranslational modifications of histones regulate processes such as transcription, replication and repair of DNA. Recently, a novel posttranslational modification has been identified: covalent binding of the vitamin biotin to lysine residues in histones, mediated by biotinidase and holocarboxylase synthetase. Here we describe a novel peptide-based technique, which was used to identify eight distinct biotinylation sites in histones H2A, H3 and H4. Biotinylation site-specific antibodies were generated to investigate biological functions of histone biotinylation. Evidence was provided that biotinylation of histones plays a role in cell proliferation, gene silencing and cellular response to DNA damage.Entities:
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Year: 2005 PMID: 15992689 PMCID: PMC1226983 DOI: 10.1016/j.jnutbio.2005.03.025
Source DB: PubMed Journal: J Nutr Biochem ISSN: 0955-2863 Impact factor: 6.048