Biological functions of biotinylated histones

NAGARAMA KOTHAPALLI, GABRIELA CAMPOREALE, ALICE KUEH, YAP C. CHEW, ANNA M. OOMMEN, JACOB B. GRIFFIN, JANOS ZEMPLENI

Ixtapa, Zihuatanejo, Mexico

Simposio; NAFTA Satellite Meeting to the XXV National Congress of Biochemistry; 2004

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.