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Location of C-protein, H-protein and X-protein in rabbit skeletal muscle fibre types

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Summary

The locations of C-protein, H-protein and X-protein in rabbit psoas, plantaris and soleus muscles have been investigated with fluorescently tagged specific antibodies. Two systems have been examined: isolated myofibrils allowed the locations of these proteins within the sarcomere to be determined, while cryosections allowed a comparison of the amounts of these proteins between different types of fibre in the three muscles.

Using antibody-labelled cryosections, we find that the amounts of each of these proteins depends closely on the fibre type. In all the muscles studied, C-protein is present in the largest amounts in fast white and fast intermediate fibres and is absent from slow red fibres, while X-protein is absent from fast white fibres and is present in the largest amounts in fast and slow red fibres. In psoas muscle, H-protein is present in the largest amounts in fast white fibres and is absent in fast and slow red fibres. In plantaris muscle, however, H-protein is absent from fast white fibres but occurs in some slow red fibres.

All psoas myofibrils label with anti-C and anti-H and a minority label with anti-X. In each case the pattern of labelling is a zone in each half of the A-band. Measured across the middle of the A-band, the zones for H-protein are much closer together than for C-protein; the centre-to-centre spacings are 0.35 µm for anti-H and 0.64 µm for anti-C. The fluorescent zones for X-protein are slightly but significantly closer (0.52 µm) than those for C-protein. All soleus myofibrils label with anti-X but the centre-to-centre spacing was greater (0.67 µm). With plantaris myofibrils, where labelling occurs with anti-C or anti-H, the spacings resemble those in psoas myofibrils, but with anti-X the spacing resembles that in soleus myofibrils.

The spacing of the fluorescent zones in an A-band, whether produced by anti-C, anti-X or anti-H does not vary with sarcomere length. We conclude that X-protein and H-protein, like C-protein, are thick filament components.

With both fibres and myofibrils, there is no simple relationship between the amount of X-protein and the amount of C-protein. Many fast intermediate fibres in psoas and plantaris muscle label as strongly with anti-C as do fast white fibres but also label as strongly with anti-X as do fast and slow red fibres. Similarly, some psoas and many plantaris myofibrils label strongly with both antibodies. We conclude that C-protein and X-protein can coexist on thick filaments but do not compete for the same sites.

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References

  • BÁRÁNY, M. (1967) ATPase activity of myosin correlated with speed of muscle shortening.J. gen. Physiol. 50, Suppl., Part 2, 197–218.

    Google Scholar 

  • BENDALL, J. R. (1973) Postmortem changes in muscle. InStructure and Function of Muscle, Vol. 2 (edited by BOURNE, G. H.), 2nd edn, pp. 243–309. London: Academic Press.

    Google Scholar 

  • BILLETER, R., HEIZMANN, C. W., HOWARD, H. & JENNY, E. (1981) Analysis of myosin light and heavy chain types in single human skeletal muscle fibres.Eur J. Biochem. 116, 389–95.

    Google Scholar 

  • CRAIG, R. W. (1977) Structure of A-segments from fro and rabbit skeletal muscle.J. molec. Biol. 109, 69–81.

    Google Scholar 

  • CRAIG, R. W. & OFFER, G. (1976) The location of C-protein in rabbit skeletal muscle.Proc. R. Soc. 192, 451–61.

    Google Scholar 

  • CRAIG, R. W. & MEGERMAN, J. (1979) Electron microscopy studies on muscle thick filaments. InMotility in Cell Function, Proceedings of First John M. Marshall Symposium in Cell Biology (edited by PEPE, F., SSANGER, J. and NACHMIAS, V.) pp. 91–102. New York: Academic Press.

    Google Scholar 

  • CALLAWAY, J. E. & BECHITEL, P. J. (1981) C-protein from rabbit soleus (red) muscle.Biochem J. 195, 363–9.

    Google Scholar 

  • DHOOT, G. K. & PERRY, S. V. (1979) Distribution of polymorphic forms of troponin components and tropomyosin in skeletal muscle.Nature 278, 714–18.

    Google Scholar 

  • ENDO, T., & MASAKI, T. (1982) Molecular properties and functionsin vitro of chicken smooth muscle α-actinin in comparison with those of striated-muscle α-actinins.J. Biochem. (Tokyo)92, 1457–68.

    Google Scholar 

  • GAUTHIER, G. F. & LOWEY, S. (1977) Polymorphism of myosin among skeletal muscle fiber types.J. Cell Biol. 74, 760–79.

    Google Scholar 

  • GAUTHIER, G. F. & LOWEY, S. (1979) Distribution of myosin isozymes among skeletal muscle fibre types.J. Cell Biol. 81, 10–25.

    Google Scholar 

  • GAUTHIER, G. F., BURKE, R. E., LOWEY, S. & HOBBS, A. W. (1983) Myosin isozymes in normal and cross-reinervated cat skeletal muscle fibers.J. Cell Biol. 97, 756–71.

    Google Scholar 

  • GUTH, L. & SAMAHA, F. J. (1970) Procedure for the histochemical demonstration of actomyosin ATPase.Expl Neurol. 28, 365–7.

    Google Scholar 

  • HUDSON, L. & HAY, F. C. (1980)Practical Immunology. 2nd edn, p 12. Oxford: Blackwell Scientific Publications.

    Google Scholar 

  • JENNY, E., WEBER, H., LUTZ, H. & BILLETER, R. (1980) Fibre populations in rabbit skeletal muscles from birth to old age. InPlasticity of Muscle (edited by PETTE, D.), pp. 97–109. Berlin, New York: de Gruyter.

    Google Scholar 

  • KNIGHT, P. J. & TRINICK, J. A. (1982) Preparation of myofibrils. InMethods in Enzymology, Vol. 85 (edited by FREDERIKSEN, D. W. and CUNNINGHAM, L. W.), pp. 9–12. New York: Academic Press.

    Google Scholar 

  • LOCKER, R. H. & HAGYARD, C. J. (1963) A cold shortening effect in beef muscles.J. Sci. Food Agric. 14, 787–93.

    Google Scholar 

  • LOWRY, O. H., LOWRY, C. V., CHI, M. M.-Y., HINTZ, C. S. & FELDER, S. (1980) Enzymological heterogeneity of human muscle fibres. InPlasticity of Muscle (edited by PETTE, D.), pp. 3–18. Berlin, New York: de Gruyter.

    Google Scholar 

  • LUTZ, H., ERMINI, M. & JENNY, E. (1978) The size of the fibre populations in rabbit skeletal muscles as revealed by indirect immunofluorescence with anti-myosin sera.Histochemistry 57, 223–35.

    Google Scholar 

  • MAXWELL, L. C., FAULKNER, J. A. & MURPHY, R. A. (1982) Relationship among fibre type, myosin ATPase activity and contractile properties.Histochem. J. 14, 981–97.

    Google Scholar 

  • MEIJER, A. E. F. H. (1968) Improved histochemical method for the demonstration of the activity of α-glucan phosphorylase.Histochemie 12, 244–52.

    Google Scholar 

  • NACHLAS, M. M., TSOU, K.-C., DE SOUSA, E., CHENG, C.-S. & SELIGMAN, A. M. (1957) Cytochemical demonstration of succinic dehydrogenase by the use of a newp-nitrophenyl substituted ditetrazole.J. Histochem. Cytochem. 5, 420–36.

    Google Scholar 

  • NAIRN, R. C. (1976)Fluorescent Protein Tracing, 4th edn. Edinburgh: Churchill Livingstone.

    Google Scholar 

  • O'BRIEN, R. A. D. & VRBOVA, G. (1980) Nerve-muscle interactions during early development. InPlasticity of Muscle (edited by PETTE, D.), pp. 287–399. Berlin, New York: de Gruyter.

    Google Scholar 

  • OFFER, G. (1972) C-protein and the periodicity in the thick filaments of vertebrate skeletal muscle.Cold Spring Harb. Symp. quant. Biol. 37, 87–93.

    Google Scholar 

  • OFFER, G., MOOS, C. & STARR, R. (1973) A new protein of the thick filaments of vertebrate skeletal myofibrils.J. molec. Biol. 74, 653–76.

    Google Scholar 

  • PEPE, F. A. & DRUCKER, B. (1975) The myosin filament. III. C-protein.J. molec. Biol. 99, 609–17.

    Google Scholar 

  • REINACH, F. C., MASAKI, T., SHAFIQ, S., OBINATA, R. & FISCHMAN, D. A. (1982) Isoforms of C-protein in adult chicken skeletal muscle: detection with monoclonal antibodies.J. Cell Biol. 95, 78–84.

    Google Scholar 

  • REINACH, F. C., MASAKI, T. & FISCHMAN, D. A. (1983) Characterisation of the C-protein from posterior latissimus dorsi muscle of the adult chicken: heterogeneity within a single sarcomere.J. Cell Biol. 96, 297–300.

    Google Scholar 

  • SALMONS, S. (1980) The response of skeletal muscles to different patterns of use — some new developments and concepts. InPlasticity of Muscle (edited by PETTE, D.), pp. 287–399. Berlin, New York: de Gruyter.

    Google Scholar 

  • SALVIATI, G., BETTO, R. & DANIELI BETTO, D. (1982) Polymorphism of myofibrillar proteins of rabbit skeletal-muscle fibres.Biochem. J. 207, 261–72.

    Google Scholar 

  • SCHACHAT, F. H., BRONSON, D. D. & McDONALD, O. B. (1980) Two kinds of slow skeletal muscle fibers which differ in their myosin light chain complements.FEBS Letts 122, 80–82.

    Google Scholar 

  • SPAMER, C. & PETTE, D. (1977) Activity patterns of phosphofructokinase, glyceraldehyde phosphate dehydrogenase, lactate dehydrogenase and malate dehydrogenase in microdissected fast and slow fibres from rabbit psoas and soleus muscle.Histochemistry 52, 201–16.

    Google Scholar 

  • SPAMER, C. & PETTE, D. (1979) Activities of malate dehydrogenase, 3-hydroxyacyl-CoA dehydrogenase and fructose-1, 6-diphosphatase with regard to metabolic subpopulations of fast and slow twitch fibres in rabbit muscles.Histochemistry 60, 9–19.

    Google Scholar 

  • SPAMER, C. & PETTE, D. (1980) Metabolic subpopulations of rabbit skeletal muscle fibres. InPlasticity of Muscle (edited by PETTE, D.), pp. 19–30. Berlin, New York: de Gruyter.

    Google Scholar 

  • SPURWAY, N. C. (1980) Histochemical typing of muscle fibres by micro-photometry. InPlasticity of Muscle (edited by PETTE, D.), pp. 31–44. Berlin, New York: de Gruyter.

    Google Scholar 

  • SPURWAY, N. C. (1981) Objective characterization of cells in terms of microscopical parameters: an example from muscle histochemistry.Histochem. J. 13, 269–317.

    Google Scholar 

  • STARR, R. & OFFER, G. (1971) Polypeptide chains of intermediate molecular weight in myosin preparations.FEBS Letts 15, 40–44.

    Google Scholar 

  • STARR, R. & OFFER, G. (1982) Preparation of C-protein, X-protein and phosphofructokinase. InMethods in Enzymology Vol. 85 (edited by FREDERIKSEN, D. W. and CUNNINGHAM, L. W.), pp. 130–8. New York: academic Press.

    Google Scholar 

  • STARR, R., & OFFER, G. (1983) H-protein and X-protein. Two new components of the thick filaments of vertebrate skeletal muscle.J. molec. Biol. 170, 675–98.

    Google Scholar 

  • WEEDS, A. G. (1980) Myosin light chains, polymorphism and fibre type. InPlasticity of Muscle (edited by PETTE, D.), pp. 55–68. Berlin, New York: de Gruyter.

    Google Scholar 

  • YAMAMOTO, K. & MOOS, C. (1983) The C-proteins of rabbit red, white, and cardiac muscles.J. biol. Chem. 258, 8395–401.

    Google Scholar 

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Starr, R., Almond, R. & Offer, G. Location of C-protein, H-protein and X-protein in rabbit skeletal muscle fibre types. J Muscle Res Cell Motil 6, 227–256 (1985). https://doi.org/10.1007/BF00713063

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