Centro de Investigación Príncipe Felipe, 46012 Valencia, Spain.
J Biol Chem. 2011 Oct 7;286(40):35030-43. doi: 10.1074/jbc.M111.249458. Epub 2011 Aug 9.
Goodpasture antigen-binding protein-1 (GPBP-1) is an exportable non-conventional Ser/Thr kinase that regulates glomerular basement membrane collagen organization. Here we provide evidence that GPBP-1 accumulates in the cytoplasm of differentiating mouse myoblasts prior to myosin synthesis. Myoblasts deficient in GPBP-1 display defective myofibril formation, whereas myofibrils assemble with enhanced efficiency in those overexpressing GPBP-1. We also show that GPBP-1 targets the previously unidentified GIP130 (GPBP-interacting protein of 130 kDa), which binds to myosin and promotes its myofibrillar assembly. This report reveals that GPBP-1 directs myofibril formation, an observation that expands its reported role in supramolecular organization of structural proteins to the intracellular compartment.
Goodpasture 抗原结合蛋白-1(GPBP-1)是一种可输出的非传统丝氨酸/苏氨酸激酶,可调节肾小球基底膜胶原组织。在这里,我们提供的证据表明,GPBP-1 在肌球蛋白合成之前在分化的小鼠成肌细胞的细胞质中积累。缺乏 GPBP-1 的成肌细胞显示出肌原纤维形成的缺陷,而在过度表达 GPBP-1 的细胞中,肌原纤维的组装效率增强。我们还表明,GPBP-1 靶向以前未被识别的 GIP130(130 kDa 的 GPBP 相互作用蛋白),GIP130 与肌球蛋白结合并促进其肌原纤维组装。本报告揭示了 GPBP-1 指导肌原纤维的形成,这一观察结果将其在结构蛋白的超分子组织中的报告作用扩展到细胞内区室。