Regulation of ATP-citrate lyase at transcriptional and post-transcriptional levels in rat liver

Biochem Biophys Res Commun. 1992 Nov 30;189(1):264-71. doi: 10.1016/0006-291x(92)91553-3.

Abstract

The amounts of ATP-citrate lyase in liver cytosol began to increase at 12 hours after refeeding a high-carbohydrate diet and further increased until 48 hours. The amounts of the ATP-citrate lyase mRNA began to increase at 6 hours and reached to a maximum level at 12 hours, followed by decrease to a very low level until 48 hours. The elevated amount of the ATP-citrate lyase mRNA reflected on the increase of ATP-citrate lyase content in the first 24 hours, but these two parameters were not paralleled thereafter. The transcriptional activity of ATP-citrate lyase gene in nuclei of rat liver began to increase at 4 hours and further increased to reach a maximum level of 24 fold at 12 hours, maintaining a high level of 17 fold until 48 hours. The elevation of transcriptional activity of ATP-citrate lyase gene preceded the increase of ATP-citrate lyase mRNA content in the liver cytosol by 2 hours, and its increasing pattern was similar to changes of mRNA content until 12 hours. However, while the transcriptional activity remained at a high level until 48 hours, the ATP-citrate lyase mRNA concentration in the cytosol decreased after 12 hours.

MeSH terms

  • ATP Citrate (pro-S)-Lyase / genetics
  • ATP Citrate (pro-S)-Lyase / metabolism*
  • Animals
  • Base Sequence
  • Blotting, Northern
  • Cytosol / enzymology
  • Dietary Carbohydrates / pharmacology*
  • Gene Expression Regulation, Enzymologic* / drug effects
  • Kinetics
  • Male
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides
  • Plasmids
  • Polymerase Chain Reaction
  • RNA Processing, Post-Transcriptional* / drug effects
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Restriction Mapping
  • Time Factors
  • Transcription, Genetic* / drug effects

Substances

  • Dietary Carbohydrates
  • Oligodeoxyribonucleotides
  • RNA, Messenger
  • ATP Citrate (pro-S)-Lyase