Molecular cloning and tissue expression of human mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase

Arch Biochem Biophys. 1995 Mar 10;317(2):385-90. doi: 10.1006/abbi.1995.1178.

Abstract

Mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) synthase is a constituent of the HMG-CoA pathway responsible for ketone body synthesis and one of its main regulatory points. We report the isolation and characterization of a 2058-bp cDNA from human liver. This cDNA encodes a polypeptide of 508 residues and 56,635 Da. The homology with previously reported rat mitochondrial and human cytosolic HMG-CoA synthases is 88 and 66%, respectively. mRNA levels were high in liver and colon, low in testis, heart, skeletal muscle, and kidney, and faint in pancreas.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cloning, Molecular*
  • Colon / enzymology
  • DNA, Complementary / chemistry
  • DNA, Complementary / isolation & purification
  • Gene Expression*
  • Humans
  • Hydroxymethylglutaryl-CoA Synthase / genetics*
  • Mitochondria, Liver / enzymology*
  • Molecular Sequence Data
  • Organ Specificity
  • Rats
  • Restriction Mapping

Substances

  • DNA, Complementary
  • Hydroxymethylglutaryl-CoA Synthase

Associated data

  • GENBANK/X83618