@article{88296,
  keywords = {Animals, Humans, signal transduction, Mice, Cell Line, Tumor, RNA, Small Interfering, Drosophila melanogaster, Cell Differentiation, Homeodomain Proteins, Nerve Tissue Proteins, Vacuolar Proton-Translocating ATPases, Adaptor Proteins, Signal Transducing, Gene Knockdown Techniques, Receptors, Notch, Basic Helix-Loop-Helix Transcription Factors, Osteoclasts, Transcription Factor HES-1},
  author = {Nilay Sethi and Yan Yan and Debra Quek and Trudi Schupbach and Yibin Kang},
  title = {Rabconnectin-3 is a functional regulator of mammalian Notch signaling.},
  abstract = {<p>The Notch signaling pathway is important for cell fate decisions in embryonic development and adult life. Defining the functional importance of the Notch pathway in these contexts requires the elucidation of essential signal transduction components that have not been fully characterized. Here, we show that Rabconnectin-3B is required for the Notch pathway in mammalian cells. siRNA-mediated silencing of Rabconnectin-3B in mammalian cells attenuated Notch signaling and disrupted the activation and nuclear accumulation of the Notch target Hes1. Rabconnectin-3B knockdown also disrupted V-ATPase activity in mammalian cells, consistent with previous observations in Drosophila. Pharmacological inhibition of the V-ATPase complex significantly reduced Notch signaling in mammalian cells. Finally, Rabconnectin-3B knockdown phenocopied functional disruption of Notch signaling during osteoclast differentiation. Collectively, these findings define an important role for Rabconnectin-3 and V-ATPase activity in the Notch signaling pathway in mammalian cells.</p>
},
  year = {2010},
  journal = {J Biol Chem},
  volume = {285},
  pages = {34757-64},
  month = {11/2010},
  issn = {1083-351X},
  doi = {10.1074/jbc.M110.158634},
  language = {eng},
}