Dystrophin and the membrane skeleton

Curr Opin Cell Biol. 1993 Feb;5(1):82-7. doi: 10.1016/s0955-0674(05)80012-2.

Abstract

Recent studies have confirmed several predictions concerning the structure and possible function of dystrophin, including a direct interaction with F-actin and an indirect interaction with laminin via linkage through a transmembrane protein complex. The results of the past year support a role for dystrophin in linking the actin cytoskeleton with the extracellular matrix in striated muscle, but they have not explained its function in other tissues.

Publication types

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

MeSH terms

  • Actins / metabolism
  • Animals
  • Cytoskeleton / ultrastructure*
  • Dystrophin / physiology*
  • Glycosylation
  • Humans
  • Microfilament Proteins / metabolism
  • Models, Molecular
  • Muscular Dystrophies / metabolism
  • Protein Processing, Post-Translational
  • Sarcolemma / ultrastructure*
  • Torpedo / metabolism

Substances

  • Actins
  • Dystrophin
  • Microfilament Proteins