BOC, an Ig superfamily member, associates with CDO to positively regulate myogenic differentiation

EMBO J. 2002 Jan 15;21(1-2):114-24. doi: 10.1093/emboj/21.1.114.

Abstract

CDO is a cell surface receptor-like protein that positively regulates myogenic differentiation. Reported here is the identification of BOC, which, with CDO, defines a newly recognized subfamily within the immunoglobulin superfamily. cdo and boc are co-expressed in muscle precursors in the developing mouse embryo. Like CDO, BOC accelerates differentiation of cultured myoblast cell lines and participates in a positive feedback loop with the myogenic transcription factor, MyoD. CDO and BOC form complexes in a cis fashion via association of both their ectodomains and their intracellular domains. A soluble fusion protein that contains the entire BOC ectodomain functions similarly to full-length BOC to promote myogenic differentiation, indicating that the intracellular region is dispensable for its activity in this system. Furthermore, a dominant-negative form of CDO inhibits the pro-myogenic effects of soluble BOC, suggesting that BOC is dependent on CDO for its activity. CDO and BOC are proposed to be components of a receptor complex that mediates some of the cell-cell interactions between muscle precursors that are required for myogenesis.

Publication types

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

MeSH terms

  • Alkaline Phosphatase / chemistry
  • Alkaline Phosphatase / genetics
  • Alkaline Phosphatase / metabolism
  • Animals
  • Cell Adhesion Molecules*
  • Cell Differentiation
  • Cell Line
  • Feedback
  • Gene Expression Regulation, Developmental
  • Genes, ras
  • Humans
  • Immunoglobulin G / chemistry
  • Immunoglobulin G / genetics
  • Immunoglobulin G / metabolism
  • Macromolecular Substances
  • Membrane Glycoproteins / chemistry
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Muscle, Skeletal / cytology*
  • Muscle, Skeletal / embryology
  • Muscle, Skeletal / metabolism*
  • Phylogeny
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Tumor Suppressor Proteins*

Substances

  • CDON protein, human
  • Cell Adhesion Molecules
  • Immunoglobulin G
  • Macromolecular Substances
  • Membrane Glycoproteins
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Tumor Suppressor Proteins
  • Alkaline Phosphatase