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Drosophila paramyosin is important for myoblast fusion and essential for myofibril formation
2 Molecular Biology Institute, San Diego State University, San Diego, CA 92182
3 Department of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK
Address correspondence to Sanford I. Bernstein, Dept. of Biology, San Diego State University, 5500 Campanile Dr., Life Sciences 371, San Diego, CA 92182-4614. Tel.: (619) 594-5629. Fax: (619) 594-5676. E-mail: sbernst{at}sunstroke.sdsu.edu
Paramyosin is a major structural protein of thick filaments in invertebrate muscles. Coiled-coil dimers of paramyosin form a paracrystalline core of these filaments, and the motor protein myosin is arranged on the core surface. To investigate the function of paramyosin in myofibril assembly and muscle contraction, we functionally disrupted the Drosophila melanogaster paramyosin gene by mobilizing a P element located in its promoter region. Homozygous paramyosin mutants die at the late embryo stage. Mutants display defects in both myoblast fusion and in myofibril assembly in embryonic body wall muscles. Mutant embryos have an abnormal body wall muscle fiber pattern arising from defects in myoblast fusion. In addition, sarcomeric units do not assemble properly and muscle contractility is impaired. We confirmed that these defects are paramyosin-specific by rescuing the homozygous paramyosin mutant to adulthood with a paramyosin transgene. Antibody analysis of normal embryos demonstrated that paramyosin accumulates as a cytoplasmic protein in early embryo development before assembling into thick filaments. We conclude that paramyosin plays an unexpected role in myoblast fusion and is important for myofibril assembly and muscle contraction.
Key Words: contractile protein; cytoskeleton; contraction; muscle; thick filament
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