Molecular cloning and nucleotide sequence of human glucocerebrosidase cDNA

Proc Natl Acad Sci U S A. 1985 Nov;82(21):7289-93. doi: 10.1073/pnas.82.21.7289.

Abstract

Mutations in the human glucocerebrosidase gene cause Gaucher disease. A cDNA clone containing the entire human glucocerebrosidase coding region from normal cells has been isolated using lambda gt11 expression libraries. The complete nucleotide sequence, a restriction map, and a hydropathy profile are presented. Hybridization to chromosome-specific DNA localizes the human glucocerebrosidase gene to chromosome 1. The likely precursor protein is 515 amino acids long. The NH2-terminal 19 amino acids constitute a leader sequence that is cleaved from the mature protein. The predicted molecular weight of the mature protein is 55,384, without glycosylation or carboxyl-terminal processing.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, 1-3
  • Cloning, Molecular
  • Cosmids
  • DNA / genetics
  • Glucosidases / genetics*
  • Glucosylceramidase / genetics*
  • Humans
  • Recombinant Proteins / genetics*

Substances

  • Recombinant Proteins
  • DNA
  • Glucosidases
  • Glucosylceramidase

Associated data

  • GENBANK/M11080
  • GENBANK/M16328