{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,13]],"date-time":"2026-05-13T12:59:42Z","timestamp":1778677182037,"version":"3.51.4"},"reference-count":44,"publisher":"American Society for Cell Biology (ASCB)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["MBoC"],"published-print":{"date-parts":[[2019,1]]},"abstract":"<jats:p>Using Drosophila melanogaster, we created the first animal models for myosin-based Freeman\u2013Sheldon syndrome (FSS), a dominant form of distal arthrogryposis defined by congenital facial and distal skeletal muscle contractures. Electron microscopy of homozygous mutant indirect flight muscles showed normal (Y583S) or altered (T178I, R672C) myofibril assembly followed by progressive disruption of the myofilament lattice. In contrast, all alleles permitted normal myofibril assembly in the heterozygous state but caused myofibrillar disruption during aging. The severity of myofibril defects in heterozygotes correlated with the level of flight impairment. Thus our Drosophila models mimic the human condition in that FSS mutations are dominant and display varied degrees of phenotypic severity. Molecular modeling indicates that the mutations disrupt communication between the nucleotide-binding site of myosin and its lever arm that drives force production. Each mutant myosin showed reduced in vitro actin sliding velocity, with the two more severe alleles significantly decreasing the catalytic efficiency of actin-activated ATP hydrolysis. The observed reductions in actin motility and catalytic efficiency may serve as the mechanistic basis of the progressive myofibrillar disarray observed in the Drosophila models as well as the prolonged contractile activity responsible for skeletal muscle contractures in FSS patients.<\/jats:p>","DOI":"10.1091\/mbc.e18-08-0526","type":"journal-article","created":{"date-parts":[[2018,10,31]],"date-time":"2018-10-31T18:49:23Z","timestamp":1541011763000},"page":"30-41","source":"Crossref","is-referenced-by-count":15,"title":["Reductions in ATPase activity, actin sliding velocity, and myofibril stability yield muscle dysfunction in<i>Drosophila<\/i>models of myosin-based Freeman\u2013Sheldon syndrome"],"prefix":"10.1091","volume":"30","author":[{"given":"Deepti S.","family":"Rao","sequence":"first","affiliation":[{"name":"Department of Biology, Molecular Biology Institute and Heart Institute, San Diego State University, San Diego, CA 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