In vivo developmental modifications of the expression of genes encoding muscle-specific enzymes in rat

J Biol Chem. 1986 Aug 5;261(22):10271-6.

Abstract

cDNA clones for rat muscle-type creatine kinase and glycogen phosphorylase and aldolase A were isolated from a rat muscle cDNA library. An additional clone recognizing an unidentified 2.7-kilobase pair mRNA species was also isolated. These cDNA clones were used as probes to investigate the expression of the corresponding mRNAs during muscle development. Two aldolase A mRNA species were detected, one of 1650 bases expressed in non-muscle tissues, fetal muscle, and adult slow-twitch muscle, the other of 1550 bases was highly specific of adult fast-twitch skeletal muscle differentiation. These aldolase A mRNAs were shown by primer extension to differ by their 5' ends. The accumulation of muscle-type phosphorylase and creatine kinase and muscle-specific aldolase A mRNA accumulation during muscle development seems to be a coordinate process occurring progressively from the 17th day of intrauterine life up to the 30th day after birth. In contrast, the 2.7-kilobase pair RNA species is maximally expressed at the 1st week after birth as is the neonatal form of myosin heavy chain mRNA.

Publication types

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

MeSH terms

  • Aging
  • Animals
  • DNA / genetics
  • DNA / isolation & purification
  • Fetus / metabolism*
  • Fructose-Bisphosphate Aldolase / metabolism*
  • Gene Expression Regulation*
  • Muscle Development*
  • Muscles / embryology
  • Muscles / enzymology
  • Nucleic Acid Hybridization
  • Phosphorylases / genetics*
  • Poly A / metabolism
  • RNA / metabolism
  • RNA, Messenger / metabolism*
  • Rats

Substances

  • RNA, Messenger
  • Poly A
  • RNA
  • DNA
  • Phosphorylases
  • Fructose-Bisphosphate Aldolase