mua-3, a gene required for mechanical tissue integrity in Caenorhabditis elegans, encodes a novel transmembrane protein of epithelial attachment complexes

J Cell Biol. 2001 Jul 23;154(2):415-26. doi: 10.1083/jcb.200103035.

Abstract

Normal locomotion of the nematode Caenorhabditis elegans requires transmission of contractile force through a series of mechanical linkages from the myofibrillar lattice of the body wall muscles, across an intervening extracellular matrix and epithelium (the hypodermis) to the cuticle. Mutations in mua-3 cause a separation of the hypodermis from the cuticle, suggesting this gene is required for maintaining hypodermal-cuticle attachment as the animal grows in size postembryonically. mua-3 encodes a predicted 3,767 amino acid protein with a large extracellular domain, a single transmembrane helix, and a smaller cytoplasmic domain. The extracellular domain contains four distinct protein modules: 5 low density lipoprotein type A, 52 epidermal growth factor, 1 von Willebrand factor A, and 2 sea urchin-enterokinase-agrin modules. MUA-3 localizes to the hypodermal hemidesmosomes and to other sites of mechanically robust transepithelial attachments, including the rectum, vulva, mechanosensory neurons, and excretory duct/pore. In addition, it is shown that MUA-3 colocalizes with cytoplasmic intermediate filaments (IFs) at these sites. Thus, MUA-3 appears to be a protein that links the IF cytoskeleton of nematode epithelia to the cuticle at sites of mechanical stress.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins*
  • Cell Adhesion / physiology
  • Cell Adhesion Molecules / genetics*
  • Cell Adhesion Molecules / metabolism*
  • Epidermal Growth Factor / genetics
  • Epithelium / metabolism*
  • Helminth Proteins / genetics
  • Helminth Proteins / metabolism
  • Hemidesmosomes / metabolism
  • Lipoprotein(a) / genetics
  • Macromolecular Substances
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Molecular Sequence Data
  • Muscles / metabolism
  • Organ Specificity
  • Protein Structure, Tertiary / physiology
  • Sequence Analysis, DNA
  • Sequence Homology, Amino Acid

Substances

  • Caenorhabditis elegans Proteins
  • Cell Adhesion Molecules
  • Helminth Proteins
  • Lipoprotein(a)
  • MUA-3 protein, C elegans
  • Macromolecular Substances
  • Membrane Proteins
  • Epidermal Growth Factor

Associated data

  • SWISSPROT/AAD29428