Cited by 494Muscle Physiology and DisordersAquaculture Nutrition and GrowthDevelopmental Biology and Gene Regulation

Growth and the regulation of myotomal muscle mass in teleost fish

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Johnston, Ian A., Bower, Neil I., Macqueen, Daniel J.·2011·Journal of Experimental Biology

Abstract

Summary: Teleost muscle first arises in early embryonic life and its development is driven by molecules present in the egg yolk and modulated by environmental stimuli including temperature and oxygen. Several populations of myogenic precursor cells reside in the embryonic somite and external cell layer and contribute to muscle fibres in embryo, larval, juvenile and adult stages. Many signalling proteins and transcription factors essential for these events are known. In all cases, myogenesis involves myoblast proliferation, migration, fusion and terminal differentiation. Maturation of the embryonic muscle is associated with motor innervation and the development of a scaffold of connective tissue and complex myotomal architecture needed to generate swimming behaviour. Adult muscle is a heterogeneous tissue composed of several cell types that interact to affect growth patterns. The development of capillary and lymphatic circulations and extramuscular organs – notably the gastrointestinal, endocrine, neuroendocrine and immune systems – serves to increase information exchange between tissues and with the external environment, adding to the complexity of growth regulation. Teleosts often exhibit an indeterminate growth pattern, with body size and muscle mass increasing until mortality or senescence occurs. The dramatic increase in myotomal muscle mass between embryo and adult requires the continuous production of muscle fibres until 40–50% of the maximum body length is reached. Sarcomeric proteins can be mobilised as a source of amino acids for energy metabolism by other tissues and for gonad generation, requiring the dynamic regulation of muscle mass throughout the life cycle. The metabolic and contractile phenotypes of muscle fibres also show significant plasticity with respect to environmental conditions, migration and spawning. Many genes regulating muscle growth are found as multiple copies as a result of paralogue retention following whole-genome duplication events in teleost lineages. The extent to which indeterminate growth, ectothermy and paralogue preservation have resulted in modifications of the genetic pathways regulating muscle growth in teleosts compared to mammals largely remains unknown. This review describes the use of compensatory growth models, transgenesis and tissue culture to explore the mechanisms of muscle growth in teleosts and provides some perspectives on future research directions.

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Authors
Johnston, I. A., Bower, N. I., & Macqueen, D. J.
Affiliations
University of St Andrews (GB)
Corresponding author
Johnston, Ian A.
Venue
Journal of Experimental Biology
Published
2011-05-15
Volume
214
Issue
10
Pages
1617-1628
ISSN
  • 0022-0949 (ISSN-L)
  • 1477-9145
OpenAlex
W2131360442
Cited by
494
References
4
Citations by year
2026: 38 · 2025: 35 · 2024: 37 · 2023: 34 · 2022: 42 · 2021: 49 · 2020: 40 · 2019: 27 · 2018: 26 · 2017: 36 · 2016: 30 · 2015: 22 · 2014: 28 · 2013: 27 · 2012: 19
FWCI
2.28
Type
journal article
Language
en
Open access
Locations
  • Journal of Experimental Biology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Scottish Funding Council
  • European Commission
  • Natural Environment Research Council (NE/E015212/1)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Aquaculture Nutrition and Growth
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords
teleosts, muscle growth regulation, myogenesis, myogenic precursor cells, myoblast fusion, indeterminate growth, compensatory growth, whole-genome duplication, ectothermy, motor innervation
MeSH terms
Animals, Fishes, Models, Biological, Species Specificity, Signal Transduction, Muscle, Skeletal, Gene Duplication, Muscle Development

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