Inhibition of histone acetylation by N-[2-(S-coenzyme A)acetyl] spermidine amide, a multisubstrate analog

J Biol Chem. 1982 Oct 25;257(20):12165-9.

Abstract

A multisubstrate analog, formed by joining coenzyme A with spermidine through an acetic acid linkage, serves as a strong inhibitor (Ki less than 10(-8) M) of the acetylation of spermidine and histones by histone acetylase purified from calf thymus. In free solutions, this analog inhibited acetylation of the various nuclear histones to a similar extent. In isolated nuclei, this analog was found to inhibit acetylation of histones H2a and H2b very much more strongly than that of histones H3 and H4.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acetylation
  • Acetyltransferases / antagonists & inhibitors
  • Animals
  • Cattle
  • Histone Acetyltransferases
  • Histones / metabolism*
  • Kinetics
  • Saccharomyces cerevisiae Proteins*
  • Spermidine / analogs & derivatives*
  • Spermidine / metabolism
  • Spermidine / pharmacology

Substances

  • Histones
  • Saccharomyces cerevisiae Proteins
  • N-(2-(S-coenzyme A)acetyl)spermidine
  • Acetyltransferases
  • Histone Acetyltransferases
  • Spermidine