Specific antibodies reveal ordered and cell-cycle-related use of histone-H4 acetylation sites in mammalian cells

Eur J Biochem. 1989 Jan 15;179(1):131-9. doi: 10.1111/j.1432-1033.1989.tb14530.x.

Abstract

Antibodies specific for the acetylated forms of histone H4 (H4) were produced in rabbits with a synthetic peptide corresponding to the 18 N-terminal residues of tetra-acetylated H4 (i.e. with acetyllysine at positions 5, 8, 12 and 16). Specificity was determined by inhibition assays using four additional peptides, each acetylated at only a single site. Using an antiserum (R6) specific for the acetylation site at Lys-5 we have estimated the proportion of Lys-5 sites acetylated in the mono-, di- and tri-acetylated forms of H4 from randomly growing human HL-60 cells. The values obtained (7%, 29% and 61% respectively) differ from those expected if acetylation were random (i.e. 25%, 50% and 75%) or if site usage followed a set order for all H4 molecules (i.e. a jump from 0% to 100%). Antibodies from a second animal (R5) bound preferentially to peptides acetylated at Lys-12 and also bound to mono-acetylated H4 relatively weakly in several cell types. In contrast, mono-acetylated H4 from metaphase HeLa cells labelled more strongly with both antisera, indicating significant acetylation at Lys-5 and Lys-12. We conclude that (1) the sites at Lys-5 and Lys-12 are under-used in mono-acetylated H4 from a variety of mammalian cell types and Lys-8 and/or Lys-16 are therefore the first to be acetylated, (2) more than one order of site usage is possible and (3) there is a metaphase-specific shift in site usage. These results suggest that H4 acetylation plays a role in the modulation of chromatin structure in mammalian cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Antibodies / chemical synthesis
  • Antibodies / immunology*
  • Antibody Affinity
  • Antibody Specificity
  • Binding Sites, Antibody*
  • Blotting, Western
  • Cell Cycle
  • Cell Line
  • Electrophoresis, Polyacrylamide Gel
  • Histones / analysis
  • Histones / immunology*
  • Humans
  • Mitosis
  • Molecular Sequence Data
  • Radioimmunoassay

Substances

  • Antibodies
  • Histones