Developmental diseases caused by impaired nucleotide sugar transporters

Glycoconj J. 2013 Jan;30(1):5-10. doi: 10.1007/s10719-012-9375-4. Epub 2012 Apr 17.

Abstract

Nucleotide sugar transporters play critical roles in glycosylation of proteins, lipids and proteoglycans, which are essential for organogenesis, development, mammalian cellular immunity and pathogenicity of human pathogenic agents. Functional deficiencies of these transporters result in global defects of glycoconjugates, which in turn lead to a diversity of biochemical, physiological and pathological phenotypes. In this short review, we will highlight human and bovine diseases caused by mutations of these transporters.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Amino Acid Sequence / genetics
  • Animals
  • Biological Transport / genetics*
  • Carbohydrate Metabolism
  • Cattle
  • Glycosylation
  • Golgi Apparatus* / metabolism
  • Golgi Apparatus* / pathology
  • Humans
  • Membrane Transport Proteins / metabolism
  • Mutation
  • Nucleotides* / genetics
  • Nucleotides* / metabolism
  • Phenotype

Substances

  • Membrane Transport Proteins
  • Nucleotides