Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscle

FEBS Lett. 1991 Jun 3;283(2):230-4. doi: 10.1016/0014-5793(91)80595-t.

Abstract

Dystrophin, which is absent in skeletal muscle of Duchenne muscular dystrophy patients, has not been considered to play a major structural role in the cell membrane of skeletal muscle because of its low abundance (approximately 0.002% of total muscle protein). Here, we have determined the relative abundance of dystrophin in a membrane cytoskeleton preparation and found that dystrophin constitutes approximately 5% of the total membrane cytoskeleton fraction of skeletal muscle sarcolemma. In addition, dystrophin can be removed from sarcolemma by alkaline treatment. Thus, our results have demonstrated that dystrophin is a major component of the subsarcolemmal cytoskeleton in skeletal muscle and suggest that dystrophin could play a major structural role in the cell membrane of skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytoskeleton / chemistry*
  • Cytoskeleton / ultrastructure
  • Dystrophin / analysis*
  • Immunoblotting
  • Mice
  • Molecular Weight
  • Muscles / chemistry*
  • Muscles / pathology
  • Muscular Dystrophy, Animal / metabolism*
  • Muscular Dystrophy, Animal / pathology
  • Rabbits
  • Sarcolemma / chemistry*
  • Sarcolemma / ultrastructure

Substances

  • Dystrophin