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Embryonic temperature and the relative timing of muscle-specific genes during development in herring (Clupea harengus L.)

Gatty Marine Laboratory, Division of Environmental and Evolutionary Biology, School of Biology, University of St Andrews, St Andrews, Fife KY16 8LB, Scotland
Present address: Department of Anatomy and Physiology, Wellcome Trust Biocentre, University of Dundee, Dundee DD1 5EH, Scotland
*Present address: Centre for Biomolecular Sciences, School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST, Scotland (e-mail: gkt{at}st-and.ac.uk)
Accepted August 13, 2001
Temperature influences many aspects of muscle development in herring (Clupea harengus). In Clyde herring, myofibril synthesis occurred later with respect to somite stage in embryos reared at 5°C compared with 12°C. The aim of the present study was to test the hypothesis that the relative timing of expression of myogenic regulatory factors (MRFs) and myosin heavy chain (MyHC) transcripts changes with developmental temperature. Reverse transcriptase/polymerase chain reaction (RT-PCR) was used to clone partial coding regions of MyoD, myogenin and MyHC from juvenile Clyde herring. Embryos were reared at 5, 8 and 12°C, and the spatial and temporal expression patterns of transcripts were investigated using cRNA probes and in situ hybridisation. Antisense probes revealed a rostralcaudal progression of all three transcripts. MyoD transcription initially took place in the adaxial cells of the unsegmented, presomitic mesoderm, whereas myogenin transcription first occurred in newly formed somites. The MyHC gene transcript was not detected until approximately nine somites had formed. Since the somite stage at which the MRFs and MyHC were first expressed was independent of temperature, the hypothesis was rejected. We suggest that the effects of temperature on myofibril synthesis must occur downstream from MyHC transcription either at the level of translation or at the assembly stage.
Key words: herring, Clupea harengus, temperature, muscle, MyoD, myogenin, myosin heavy chain.
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