期刊
DEVELOPMENTAL BIOLOGY
卷 499, 期 -, 页码 47-58出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2023.04.002
关键词
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Slow myosin heavy chain 1 (Smyhc1) is crucial for early contraction of slow skeletal muscle fibers in zebrafish. Mutant alleles lacking smyhc1 function exhibit motility defects, but regain it as fast muscle fibers develop. However, they still experience slow muscle motility issues until about 1 month of age. Further analysis reveals that mutant slow fibers undergo normal differentiation and migration, but fail to generate large myofibrils and maintain cellular orientation due to maturation defects.
Slow myosin heavy chain 1 (Smyhc1) is the major sarcomeric myosin driving early contraction by slow skeletal muscle fibres in zebrafish. New mutant alleles lacking a functional smyhc1 gene move poorly, but recover motility as the later-formed fast muscle fibres of the segmental myotomes mature, and are adult viable. By motility analysis and inhibiting fast muscle contraction pharmacologically, we show that a slow muscle motility defect persists in mutants until about 1 month of age. Breeding onto a genetic background marking slow muscle fibres with EGFP revealed that mutant slow fibres undergo terminal differentiation, migration and fibre formation indistinguishable from wild type but fail to generate large myofibrils and maintain cellular orientation and attachments. In mutants, initial myofibrillar structures with 1.67 mu m periodic actin bands fail to mature into the 1.96 mu m sarcomeres observed in wild type, despite the presence of alternative myosin heavy chain molecules. The poorly-contractile mutant slow muscle cells generate numerous cytoplasmic organelles, but fail to grow and bundle myofibrils or to increase in cytoplasmic volume despite passive movements imposed by fast muscle. The data show that both slow myofibril maturation and cellular volume increase depend on the function of a specific myosin isoform and suggest that appropriate force production regulates muscle fibre growth.
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