Literature DB >> 16644798

Myosin heavy chain isoform composition and stretch activation kinetics in single fibres of Xenopus laevis iliofibularis muscle.

Olena Andruchova1, Gabriela M M Stephenson, Oleg Andruchov, D George Stephenson, Stefan Galler.   

Abstract

Skeletal muscle is composed of specialized fibre types that enable it to fulfil complex and variable functional needs. Muscle fibres of Xenopus laevis, a frog formerly classified as a toad, were the first to be typed based on a combination of physiological, morphological, histochemical and biochemical characteristics. Currently the most widely accepted criterion for muscle fibre typing is the myosin heavy chain (MHC) isoform composition because it is assumed that variations of this protein are the most important contributors to functional diversity. Yet this criterion has not been used for classification of Xenopus fibres due to the lack of an effective protocol for MHC isoform analysis. In the present study we aimed to resolve and visualize electrophoretically the MHC isoforms expressed in the iliofibularis muscle of Xenopus laevis, to define their functional identity and to classify the fibres based on their MHC isoform composition. Using a SDS-PAGE protocol that proved successful with mammalian muscle MHC isoforms, we were able to detect five MHC isoforms in Xenopus iliofibularis muscle. The kinetics of stretch-induced force transients (stretch activation) produced by a fibre was strongly correlated with its MHC isoform content indicating that the five MHC isoforms confer different kinetics characteristics. Hybrid fibre types containing two MHC isoforms exhibited stretch activation kinetics parameters that were intermediate between those of the corresponding pure fibre types. These results clearly show that the MHC isoforms expressed in Xenopus muscle are functionally different thereby validating the idea that MHC isoform composition is the most reliable criterion for vertebrate skeletal muscle fibre type classification. Thus, our results lay the foundation for the unequivocal classification of the muscle fibres in the Xenopus iliofibularis muscle and for gaining further insights into skeletal muscle fibre diversity.

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Year:  2006        PMID: 16644798      PMCID: PMC1817808          DOI: 10.1113/jphysiol.2006.109926

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  41 in total

1.  Ca2+_, Sr2+_force relationships and kinetic properties of fast-twitch rat leg muscle fibre subtypes.

Authors:  S Galler
Journal:  Acta Physiol Scand       Date:  1999-10

2.  Kinetic properties of myosin heavy chain isoforms in single fibers from human skeletal muscle.

Authors:  K Hilber; S Galler; B Gohlsch; D Pette
Journal:  FEBS Lett       Date:  1999-07-23       Impact factor: 4.124

Review 3.  Mechanics and models of the myosin motor.

Authors:  A F Huxley
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-04-29       Impact factor: 6.237

4.  An electrophoretic study of myosin heavy chain expression in skeletal muscles of the toad Bufo marinus.

Authors:  L T Nguyen; G M Stephenson
Journal:  J Muscle Res Cell Motil       Date:  1999-10       Impact factor: 2.698

5.  Kinetic properties of myosin heavy chain isoforms in mouse skeletal muscle: comparison with rat, rabbit, and human and correlation with amino acid sequence.

Authors:  Oleg Andruchov; Olena Andruchova; Yishu Wang; Stefan Galler
Journal:  Am J Physiol Cell Physiol       Date:  2004-08-11       Impact factor: 4.249

6.  Electrophoretic and functional identification of two troponin C isoforms in toad skeletal muscle fibers.

Authors:  Brett O'Connell; Ronnie Blazev; Gabriela M M Stephenson
Journal:  Am J Physiol Cell Physiol       Date:  2005-09-21       Impact factor: 4.249

Review 7.  Hybrid skeletal muscle fibres: a rare or common phenomenon?

Authors:  G M Stephenson
Journal:  Clin Exp Pharmacol Physiol       Date:  2001-08       Impact factor: 2.557

Review 8.  Functional heterogeneity of mammalian single muscle fibres: do myosin isoforms tell the whole story?

Authors:  R Bottinelli
Journal:  Pflugers Arch       Date:  2001-10       Impact factor: 3.657

9.  Dependence of cross-bridge kinetics on myosin light chain isoforms in rabbit and rat skeletal muscle fibres.

Authors:  Oleg Andruchov; Olena Andruchova; Yishu Wang; Stefan Galler
Journal:  J Physiol       Date:  2005-12-15       Impact factor: 5.182

10.  Identification of myosin light chains in Rana pipiens skeletal muscle and their expression patterns along single fibres.

Authors:  G J Lutz; S N Bremner; M J Bade; R L Lieber
Journal:  J Exp Biol       Date:  2001-12       Impact factor: 3.312

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  5 in total

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Authors:  D George Stephenson
Journal:  J Muscle Res Cell Motil       Date:  2006-07-28       Impact factor: 2.698

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Authors:  Cuiping Zhao; Douglas M Swank
Journal:  Am J Physiol Cell Physiol       Date:  2016-11-23       Impact factor: 4.249

3.  An embryonic myosin isoform enables stretch activation and cyclical power in Drosophila jump muscle.

Authors:  Cuiping Zhao; Douglas M Swank
Journal:  Biophys J       Date:  2013-06-18       Impact factor: 4.033

4.  The influence of jaw-muscle fibre-type phenotypes on estimating maximum muscle and bite forces in primates.

Authors:  Megan Holmes; Andrea B Taylor
Journal:  Interface Focus       Date:  2021-08-13       Impact factor: 3.906

5.  The genome of the diploid anuran Xenopus tropicalis contains a novel array of sarcoplasmic myosin heavy chain genes expressed in larval muscle and larynx.

Authors:  Brian T Nasipak; Darcy B Kelley
Journal:  Dev Genes Evol       Date:  2008-06-13       Impact factor: 0.900

  5 in total

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