• Title of article

    Biological functions of biotinylated histones

  • Author/Authors

    Nagarama Kothapalli، نويسنده , , Gabriela Camporeale، نويسنده , , Alice Kueh، نويسنده , , Yap C. Chew، نويسنده , , Anna M. Oommen، نويسنده , , Jacob B. Griffin، نويسنده , , Janos Zempleni، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2005
  • Pages
    3
  • From page
    446
  • To page
    448
  • 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.
  • Keywords
    DNA damage , Epigenetics , Histones , Human , Biotin , Chromatin
  • Journal title
    The Journal of Nutritional Biochemistry
  • Serial Year
    2005
  • Journal title
    The Journal of Nutritional Biochemistry
  • Record number

    1297113