ArticleThe Journal of physiology1998
Four novel myosin heavy chain transcripts define a molecular basis for muscle fibre types in Rana pipiens.
Article in The Journal of physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 48 citations in OpenAlex.
- Developmental, physiologic and phylogenetic perspectives on the expression and regulation of myosin heavy chains in mammalian skeletal muscles.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2023Review
- Recovery of rat muscle size but not function more than 1 year after a single botulinum toxin injection.Muscle & nerve · 2018Article
- Differential susceptibility on myosin heavy chain isoform following eccentric-induced muscle damage.Journal of exercise rehabilitation · 2014Review
- Enzyme activity in the aestivating green-striped burrowing frog (Cyclorana alboguttata).Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2010Article
- The genome of the diploid anuran Xenopus tropicalis contains a novel array of sarcoplasmic myosin heavy chain genes expressed in larval muscle and larynx.Development genes and evolution · 2008Article
- Selection for antimicrobial peptide diversity in frogs leads to gene duplication and low allelic variation.Journal of molecular evolution · 2007Article
- Myosin heavy chain isoform composition and stretch activation kinetics in single fibres of Xenopus laevis iliofibularis muscle.The Journal of physiology · 2006Article
- In vivo expression of myosin essential light chain using plasmid expression vectors in regenerating frog skeletal muscle.Gene therapy · 2005Article
- Contractile properties of isolated muscle spindles of the frog.The Journal of physiology · 2002Article
- Myosin heavy chain isoform expression and Ca2 +-stimulated ATPase activity in single fibres of toad rectus abdominis muscle.Journal of muscle research and cell motility · 2002Article
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Authors and funding
4 authors at 2 institutions in 2 countries.
Funding
Abstract
1. Differential expression of myosin heavy chain (MHC) isoforms dramatically affects mechanical and energetic properties of skeletal muscle fibre types. As many as five different fibre types, each with different mechanical properties, have been reported in frog hindlimb muscles. However, only two frog MHC isoforms have previously been detected by SDS-PAGE and only one adult hindlimb MHC isoform has been cloned. 2. In the present study, four different fibre types (type 1, type 2, type 3 and tonic) were initially identified in adult Rana pipiens anterior tibialis muscle based on myosin ATPase histochemistry, size and location. Each fibre type exhibited unique reactivity to a panel of MHC monoclonal antibodies. Single fibre analysis using SDS-PAGE revealed that MHCs from immunohistochemically defined type 1, type 2 and type 3 fibres ran as three distinct isoform bands, while MHC of tonic fibres co-migrated with type 1 MHC. The combined data from immunohistochemistry and SDS-PAGE suggests that Rana fibre types are composed of four different MHCs. 3. Four novel MHC cDNAs were cloned and expression of the corresponding transcripts was measured in single immuno-identified fibres using specific polymerase chain reaction (PCR) primer pairs. Each of the four transcripts was found to be primarily expressed in a different one of the four fibre types. 4. Coexpression of MHC isoforms was observed only between types 1/2 and types 2/3 at both the protein and mRNA level. 5. These data provide a molecular basis for differentiation between frog fibre types and permit future molecular studies of MHC structure/function and gene regulation in this classic physiological system. 6. Comparison of sequence homology among amphibian, avian and mammalian MHC families supports the concept of independent evolution of fast MHC genes within vertebrate classes subsequent to the amphibian/avian/mammalian radiation.
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