Mammalian O-mannosylation: unsolved questions of structure/function

Curr Opin Struct Biol. 2011 Oct;21(5):603-9. doi: 10.1016/j.sbi.2011.09.001. Epub 2011 Sep 22.

Abstract

Post-translational modification of polypeptides with glycans increases the diversity of the structures of proteins and imparts increased functional diversity. Here, we review the current literature on a relatively new O-glycosylation pathway, the mammalian O-mannosylation pathway. The importance of O-mannosylation is illustrated by the fact that O-mannose glycan structures play roles in a variety of processes including viral entry into cells, metastasis, cell adhesion, and neuronal development. Furthermore, mutations in the enzymes of this pathway are causal for a variety of congenital muscular dystrophies. Here we highlight the protein substrates, glycan structures, and enzymes involved in O-mannosylation as well as our gaps in understanding structure/function relationships in this biosynthetic pathway.

Publication types

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

MeSH terms

  • Animals
  • Brain / abnormalities
  • Dystroglycans / genetics
  • Dystroglycans / metabolism*
  • Dystrophin / genetics
  • Dystrophin / metabolism
  • Glycosylation
  • Humans
  • Mammals
  • Mannose / metabolism*
  • Mannosyltransferases / genetics
  • Mannosyltransferases / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Muscular Dystrophies / genetics
  • Muscular Dystrophies / physiopathology
  • Mutation
  • Polysaccharides / metabolism*
  • Protein Processing, Post-Translational*
  • Structure-Activity Relationship

Substances

  • Dystrophin
  • FKTN protein, human
  • Membrane Proteins
  • Polysaccharides
  • Dystroglycans
  • Mannosyltransferases
  • glycolipid 3-alpha-mannosyltransferase
  • Mannose