Molecular cloning and sequencing of human palmitoyl-CoA ligase and its tissue specific expression

Mol Cell Biochem. 1995 Oct 4;151(1):77-81. doi: 10.1007/BF01076899.

Abstract

A complimentary DNA clone encoding the entire human palmitoyl-CoA ligase has been isolated from a liver cDNA library and sequenced in it's entirety. The predicted product is a 699 amino acid protein. Southern analysis utilizing the human palmitoyl-CoA ligase gene as a probe revealed varying degrees of similarity amongst various mammalian species. The palmitoyl-CoA ligase gene is highly expressed in liver, heart, skeletal muscle and kidney, and to a lesser extent in brain, lung, placenta and pancreas. The expression of palmitoyl-CoA ligase in various tissue parallels the function of this enzyme in the metabolism of fatty acids in these tissues.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Cloning, Molecular
  • Coenzyme A Ligases / chemistry*
  • Coenzyme A Ligases / genetics
  • Humans
  • Molecular Sequence Data
  • Organ Specificity
  • Repressor Proteins*
  • Saccharomyces cerevisiae Proteins*
  • Sequence Homology, Amino Acid
  • Species Specificity

Substances

  • Repressor Proteins
  • Saccharomyces cerevisiae Proteins
  • Coenzyme A Ligases
  • FAA2 protein, S cerevisiae
  • long-chain-fatty-acid-CoA ligase

Associated data

  • GENBANK/L09229