| Literature DB >> 21832087 |
Francisco Revert-Ros1, Ernesto López-Pascual, Froilán Granero-Moltó, Jesús Macías, Richard Breyer, Roy Zent, Billy G Hudson, Anas Saadeddin, Fernando Revert, Raül Blasco, Carmen Navarro, Deborah Burks, Juan Saus.
Abstract
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.Entities:
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Year: 2011 PMID: 21832087 PMCID: PMC3186396 DOI: 10.1074/jbc.M111.249458
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157