McArdle's & Hers' diseases: glycogen phosphorylase transcriptional expression in human tissues

J Neurogenet. 1987 Dec;4(6):293-308.

Abstract

We have cloned the cDNA encoding human liver glycogen phosphorylase (glycogenosis type VI) from a fetal brain cDNA library. Liver(L) and muscle(M) phosphorylase cDNA probes were used to determine the relative abundance of mRNA encoding the L- and M-isozymes of phosphorylase in human fetal and adult tissues. The transcript encoding the M-isozyme is 3.4 kb; the L-isozyme transcript is 3.3 kb. Transcriptional expression of the L-isozyme in human and primate tissues was found to differ from the isozyme's reported tissue specificity in non-primate mammals. Furthermore, using degenerate oligonucleotide probes to two different coding regions of M-phosphorylase, a novel 4.1-kb transcript was demonstrated to be present in human fetal and adult brain.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Brain / enzymology
  • Cloning, Molecular
  • DNA / genetics
  • Fetus
  • Glycogen Storage Disease / enzymology*
  • Glycogen Storage Disease Type III / enzymology*
  • Glycogen Storage Disease Type III / genetics
  • Glycogen Storage Disease Type VI / enzymology*
  • Glycogen Storage Disease Type VI / genetics
  • Humans
  • Isoenzymes / genetics*
  • Liver / enzymology
  • Molecular Sequence Data
  • Muscles / enzymology
  • Phosphorylases / genetics*
  • RNA, Messenger / genetics
  • Rabbits
  • Sequence Homology, Nucleic Acid
  • Transcription, Genetic*

Substances

  • Isoenzymes
  • RNA, Messenger
  • DNA
  • Phosphorylases