Rat ATP citrate-lyase. Molecular cloning and sequence analysis of a full-length cDNA and mRNA abundance as a function of diet, organ, and age
- PMID: 2295639
Rat ATP citrate-lyase. Molecular cloning and sequence analysis of a full-length cDNA and mRNA abundance as a function of diet, organ, and age
Abstract
ATP citrate-lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. We have isolated a full-length cDNA copy of 4.3 kilobase pairs encoding the ATP-citrate lyase mRNA by screening rat liver cDNA library using oligonucleotide probes designed from peptide sequences obtained from the purified rat enzyme. Expression of this cDNA in bacteria, followed by immunoblotting with antibody directed against the ATP citrate-lyase, further demonstrated the identity of this clone. Nucleic acid sequence data indicate that the cDNA contains the complete coding region for the enzyme, which is 1100 amino acids in length with a calculated molecular weight of 121,293. RNA blot analysis indicated an mRNA species of about 4.3 kilobase pairs in livers of chow-fed rats. Rats maintained on low fat, high carbohydrate diets exhibited a striking increase (50-fold) in the level of liver ATP citrate-lyase mRNA as compared with the control animals maintained on a normal diet. The tissue distribution of this mRNA in chow-fed animals revealed a relatively high abundance of the message in liver and adrenal, moderate levels were found in lung, brain, and large intestine with only trace amounts of the message in small intestine, stomach, testis, spleen, pancreas, kidney, and heart. During rat development, the ATP citrate-lyase mRNA was relatively high in the liver at parturition, followed by a reduction in its level during suckling. Higher amounts of the mRNA were detected again in adult animals. The isolation and characterization of the mRNA for ATP citrate-lyase will allow further studies on the reaction mechanism and metabolic regulation of this key enzyme in lipogenesis and cholesterogenesis.
Similar articles
-
Cloning and expression of a human ATP-citrate lyase cDNA.Eur J Biochem. 1992 Mar 1;204(2):491-9. doi: 10.1111/j.1432-1033.1992.tb16659.x. Eur J Biochem. 1992. PMID: 1371749
-
Cloning of cDNA sequences for murine ATP-citrate lyase. Construction of recombinant plasmids using an immunopurified mRNA template and evidence for the nutritional regulation of ATP-citrate lyase mRNA content in mouse liver.J Biol Chem. 1984 Jan 25;259(2):1201-5. J Biol Chem. 1984. PMID: 6546379
-
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. Biochem Biophys Res Commun. 1992. PMID: 1449481
-
Effects of nutrients and hormones on gene expression of ATP citrate-lyase in rat liver.Eur J Biochem. 1992 Oct 1;209(1):217-22. doi: 10.1111/j.1432-1033.1992.tb17279.x. Eur J Biochem. 1992. PMID: 1396700
-
ATP-citrate lyase: a driver of metabolism and histone acetylation.Curr Opin Lipidol. 2020 Dec;31(6):362-363. doi: 10.1097/MOL.0000000000000719. Curr Opin Lipidol. 2020. PMID: 33149082 Review. No abstract available.
Cited by
-
AMP-activated protein kinase and ATP-citrate lyase are two distinct molecular targets for ETC-1002, a novel small molecule regulator of lipid and carbohydrate metabolism.J Lipid Res. 2013 Jan;54(1):134-51. doi: 10.1194/jlr.M030528. Epub 2012 Nov 1. J Lipid Res. 2013. PMID: 23118444 Free PMC article.
-
New perspectives in the regulation of hepatic glycolytic and lipogenic genes by insulin and glucose: a role for the transcription factor sterol regulatory element binding protein-1c.Biochem J. 2002 Sep 1;366(Pt 2):377-91. doi: 10.1042/BJ20020430. Biochem J. 2002. PMID: 12061893 Free PMC article. Review.
-
The role of ATP citrate-lyase in the metabolic regulation of plasma lipids. Hypolipidaemic effects of SB-204990, a lactone prodrug of the potent ATP citrate-lyase inhibitor SB-201076.Biochem J. 1998 Aug 15;334 ( Pt 1)(Pt 1):113-9. doi: 10.1042/bj3340113. Biochem J. 1998. PMID: 9693110 Free PMC article.
-
Compartmentation of ATP:citrate lyase in plants.Plant Physiol. 2000 Apr;122(4):1225-30. doi: 10.1104/pp.122.4.1225. Plant Physiol. 2000. PMID: 10759519 Free PMC article.
-
Comparative genomic analysis of carbon and nitrogen assimilation mechanisms in three indigenous bioleaching bacteria: predictions and validations.BMC Genomics. 2008 Dec 3;9:581. doi: 10.1186/1471-2164-9-581. BMC Genomics. 2008. PMID: 19055775 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases