Clathrin isoform CHC22, a component of neuromuscular and myotendinous junctions, binds sorting nexin 5 and has increased expression during myogenesis and muscle regeneration

Mol Biol Cell. 2004 Jul;15(7):3181-95. doi: 10.1091/mbc.e04-03-0249. Epub 2004 May 7.

Abstract

The muscle isoform of clathrin heavy chain, CHC22, has 85% sequence identity to the ubiquitously expressed CHC17, yet its expression pattern and function appear to be distinct from those of well-characterized clathrin-coated vesicles. In mature muscle CHC22 is preferentially concentrated at neuromuscular and myotendinous junctions, suggesting a role at sarcolemmal contacts with extracellular matrix. During myoblast differentiation, CHC22 expression is increased, initially localized with desmin and nestin and then preferentially segregated to the poles of fused myoblasts. CHC22 expression is also increased in regenerating muscle fibers with the same time course as embryonic myosin, indicating a role in muscle repair. CHC22 binds to sorting nexin 5 through a coiled-coil domain present in both partners, which is absent in CHC17 and coincides with the region on CHC17 that binds the regulatory light-chain subunit. These differential binding data suggest a mechanism for the distinct functions of CHC22 relative to CHC17 in membrane traffic during muscle development, repair, and at neuromuscular and myotendinous junctions.

Publication types

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

MeSH terms

  • Animals
  • Carrier Proteins / metabolism*
  • Cell Line
  • Clathrin / metabolism*
  • Clathrin Heavy Chains / analysis
  • Clathrin Heavy Chains / genetics
  • Clathrin Heavy Chains / metabolism*
  • Cobra Cardiotoxin Proteins / pharmacology
  • Desmin / analysis
  • Desmin / metabolism
  • Humans
  • Integrins / analysis
  • Integrins / metabolism
  • Intermediate Filament Proteins / analysis
  • Intermediate Filament Proteins / metabolism
  • Muscle Development*
  • Muscle Proteins / analysis
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Muscle, Skeletal / growth & development
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiology*
  • Nerve Tissue Proteins / analysis
  • Nerve Tissue Proteins / metabolism
  • Nestin
  • Neuromuscular Junction / chemistry
  • Neuromuscular Junction / metabolism*
  • Protein Transport
  • Regeneration*
  • Sorting Nexins
  • Tendons / immunology
  • Tendons / metabolism
  • Two-Hybrid System Techniques
  • Vesicular Transport Proteins

Substances

  • CLTCL1 protein, human
  • Carrier Proteins
  • Clathrin
  • Cobra Cardiotoxin Proteins
  • Desmin
  • Integrins
  • Intermediate Filament Proteins
  • Muscle Proteins
  • NES protein, human
  • Nerve Tissue Proteins
  • Nestin
  • SNX5 protein, human
  • Sorting Nexins
  • Vesicular Transport Proteins
  • Clathrin Heavy Chains
  • integrin alpha7beta1