Etard Christelle, Behra Martine, Fischer Nadine, Hutcheson David, Geisler Robert, Strähle Uwe
Institut de Génétique et de Biologie Moléculaire et Cellulaire, 1 rue Laurent Fries, 67404 Illkirch Cedex, CU de Strasbourg, France.
Dev Biol. 2007 Aug 1;308(1):133-43. doi: 10.1016/j.ydbio.2007.05.014. Epub 2007 May 18.
Contraction of muscles is mediated by highly organized arrays of myosin motor proteins. We report here the characterization of a mutation of a UCS gene named steif/unc-45b that is required for the formation of ordered myofibrils in both the skeletal and cardiac muscles of zebrafish. We show that Steif/Unc-45b interacts with the chaperone Hsp90a in vitro. The two genes are co-expressed in the skeletal musculature and knockdown of Hsp90a leads to impaired myofibril formation in the same manner as lack of Steif/Unc-45b activity. Transcripts of both genes are up-regulated in steif mutants suggesting co-regulation of the two genes. Our data indicate a requirement of Steif/unc-45b and Hsp90a for the assembly of the contractile apparatus in the vertebrate skeletal musculature.
肌肉收缩由高度有序排列的肌球蛋白运动蛋白介导。我们在此报告了一个名为steif/unc-45b的UCS基因突变的特征,该基因对于斑马鱼骨骼肌和心肌中有序肌原纤维的形成是必需的。我们表明,Steif/Unc-45b在体外与伴侣蛋白Hsp90a相互作用。这两个基因在骨骼肌组织中共同表达,敲低Hsp90a会导致肌原纤维形成受损,其方式与缺乏Steif/Unc-45b活性相同。两个基因的转录本在steif突变体中均上调,表明这两个基因存在共同调控。我们的数据表明,Steif/unc-45b和Hsp90a是脊椎动物骨骼肌组织中收缩装置组装所必需的。