The inside and out of dystroglycan post-translational modification

Neuromuscul Disord. 2012 Nov;22(11):959-65. doi: 10.1016/j.nmd.2012.05.016. Epub 2012 Jul 4.

Abstract

In neuromuscular systems dystroglycan provides a vital link between laminin in the extracellular matrix and dystrophin in the membrane cytoskeleton. The integrity of this link is maintained and regulated by post-translational modifications of dystroglycan that have effects both inside and outside the cell. Glycosylation of α-dystroglycan is crucial for its link to laminin and phosphorylation of β-dystroglycan on tyrosine regulates its association with intracellular binding partners. This short review focuses on some of the recent developments in our understanding of the role of these post-translational modification in regulating dystroglycan function, and how new knowledge of signalling through the laminin-dystroglycan axis is leading to hope for treatment for some neuromuscular diseases associated with this adhesion complex.

Publication types

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

MeSH terms

  • Animals
  • Dystroglycans / genetics
  • Dystroglycans / metabolism*
  • Dystrophin / genetics
  • Dystrophin / metabolism*
  • Humans
  • Laminin / genetics
  • Laminin / metabolism
  • Mutation / genetics
  • N-Acetylglucosaminyltransferases / genetics
  • N-Acetylglucosaminyltransferases / metabolism
  • Protein Processing, Post-Translational*

Substances

  • Dystrophin
  • Laminin
  • Dystroglycans
  • LARGE1 protein, human
  • N-Acetylglucosaminyltransferases