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
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
Journal title :
The Journal of Nutritional Biochemistry