Expression of multiple slow myosin heavy chain genes reveals a diversity of zebrafish slow twitch muscle fibres with differing requirements for Hedgehog and Prdm1 activity

Elworthy, S., Hargrave, M., Knight, R., Mebus, K., and Ingham, P.W.
Development (Cambridge, England)   135(12): 2115-2126 (Journal)
Registered Authors
Elworthy, Stone, Hargrave, Murray, Ingham, Philip, Knight, Robert
Zebrafish, Myotome, Fibre type, Slow myosin heavy chain, Troponin, Prox1, Shh, Blimp1, u-boot, prdm1, Craniofacial
MeSH Terms
  • Animals
  • DNA-Binding Proteins/genetics
  • DNA-Binding Proteins/physiology*
  • Embryo, Nonmammalian
  • Fluorescent Antibody Technique, Direct
  • Gene Expression/physiology
  • Genetic Heterogeneity
  • Hedgehog Proteins/genetics
  • Hedgehog Proteins/physiology*
  • In Situ Hybridization
  • Muscle Fibers, Slow-Twitch/cytology
  • Muscle Fibers, Slow-Twitch/physiology*
  • Myosin Heavy Chains/genetics*
  • Myosin Heavy Chains/metabolism
  • Nuclear Proteins/genetics
  • Nuclear Proteins/physiology*
  • Transgenes
  • Zebrafish/embryology*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/physiology*
18480160 Full text @ Development
The zebrafish embryo develops a series of anatomically distinct slow twitch muscle fibres that characteristically express genes encoding lineage-specific isoforms of sarcomeric proteins such as MyHC and troponin. We show here that different subsets of these slow fibres express distinct members of a tandem array of slow MyHC genes. The first slow twitch muscle fibres to differentiate, which are specified by the activity of the transcription factor Prdm1 (also called Ubo or Blimp1) in response to Hedgehog (Hh) signalling, express the smyhc1 gene. Subsequently, secondary slow twitch fibres differentiate in most cases independently of Hh activity. We find that although some of these later-forming fibres also express smyhc1, others express smyhc2 or smyhc3. We show that the smyhc1-positive fibres express the ubo (prdm1) gene and adopt fast twitch fibre characteristics in the absence of Prdm1 activity, whereas those that do not express smyhc1 can differentiate independently of Prdm1 function. Conversely, some smyhc2-expressing fibres, although independent of Prdm1 function, require Hh activity to form. The adult trunk slow fibres express smyhc2 and smyhc3, but lack smyhc1 expression. The different slow fibres in the craniofacial muscles variously express smyhc1, smyhc2 and smyhc3, and all differentiate independently of Prdm1.
Genes / Markers
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Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Engineered Foreign Genes
Errata and Notes