Modification of protein synthetic components by aflatoxin B1

Biochem Pharmacol. 1988 Apr 15;37(8):1481-6. doi: 10.1016/0006-2952(88)90009-3.

Abstract

Molecular sites of perturbation by the hepatocarcinogen aflatoxin B1 (AFB1) in the protein synthesis initiation complex were assessed using isolated hepatocytes and a cell-free activating system containing microsomes and cytoplasmic ribonucleoprotein complexes (cRPC). Ribosomal proteins showed no detectable modification by the toxin in either system. With hepatocytes, initiation factors demonstrated only slight modification by AFB1. RNAs from both hepatocytes and the cell-free system with microsomes and cRPC were modified, with poly(A)-containing RNA exhibiting at least a 5-fold higher modification than poly(A)-lacking RNA. The poly(A)-lacking RNAs were modified in the order 28S rRNA greater than 18S rRNA greater than 5-6S rRNA greater than 4S tRNA. Guanine was the target base of AFB1, but only 10% of the AFB1-GMP adducts were on guanines located in a poly(G) region. These results suggest that guanine modification in RNAs may be responsible for the observed inhibition of translational initiation by AFB1 to a greater extent than modification of either ribosomal intrinsic or associated proteins.

Publication types

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

MeSH terms

  • Aflatoxin B1
  • Aflatoxins / metabolism
  • Aflatoxins / pharmacology*
  • Animals
  • Binding Sites
  • Hydrolysis
  • In Vitro Techniques
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Peptide Initiation Factors / metabolism
  • Protein Binding
  • Protein Biosynthesis*
  • RNA, Messenger / drug effects
  • Rats
  • Rats, Inbred Strains
  • Ribonucleoproteins / metabolism
  • Ribosomal Proteins / metabolism
  • Subcellular Fractions / drug effects
  • Subcellular Fractions / metabolism

Substances

  • Aflatoxins
  • Peptide Initiation Factors
  • RNA, Messenger
  • Ribonucleoproteins
  • Ribosomal Proteins
  • Aflatoxin B1