Foot protein isoforms are expressed at different times during embryonic chick skeletal muscle development

J Cell Biol. 1991 May;113(4):793-803. doi: 10.1083/jcb.113.4.793.

Abstract

We have investigated the time course of expression of the alpha and beta triad junctional foot proteins in embryonic chick pectoral muscle. The level of [3H]ryanodine binding in muscle homogenates is low until day E20 of embryonic development, then increases dramatically at the time of hatching reaching adult levels by day N7 posthatch. The alpha and beta foot protein isoforms increase in abundance concomitantly with [3H]ryanodine binding. Using foot protein isoform-specific antibodies, the alpha foot protein is detected in a majority of fibers in day E10 muscle, while the beta isoform is first observed at low levels in a few fibers in day E15 muscle. A high molecular weight polypeptide, distinct from the alpha and beta proteins, is recognized by antifoot protein antibodies. This polypeptide is observed in day E8 muscle and declines in abundance with continued development. It appears to exist as a monomer and does not bind [3H]ryanodine. In contrast, the alpha isoform present in day E10 muscle and the beta isoform in day E20 muscle are oligomeric and bind [3H]ryanodine suggesting that they may exist as functional calcium channels in differentiating muscle. Comparison of the intracellular distributions of the alpha foot protein, f-actin, the heavy chain of myosin and titin in day E10 muscle indicates that the alpha foot protein is expressed during myofibril assembly and Z line formation. The differential expression of the foot protein isoforms in developing muscle, and their continued expression in mature muscle, is consistent with these proteins making different functional contributions. In addition, the expression of the alpha isoform during the time of organization of a differentiated muscle morphology suggests that foot proteins may participate in events involved in muscle differentiation.

Publication types

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

MeSH terms

  • Actins / metabolism
  • Age Factors
  • Animals
  • Blotting, Western
  • Cell Differentiation
  • Chick Embryo
  • Connectin
  • Fluorescent Antibody Technique
  • Molecular Weight
  • Muscle Proteins / metabolism
  • Muscles / embryology*
  • Muscles / metabolism
  • Precipitin Tests
  • Protein Kinases*
  • Receptors, Cholinergic / chemistry
  • Receptors, Cholinergic / immunology
  • Receptors, Cholinergic / metabolism*
  • Ryanodine Receptor Calcium Release Channel

Substances

  • Actins
  • Connectin
  • Muscle Proteins
  • Receptors, Cholinergic
  • Ryanodine Receptor Calcium Release Channel
  • Protein Kinases