| Literature DB >> 24103590 |
Junwen Zhang1, Wen Ma, Shuo Tian, Zhenzhen Fan, Xiaoli Ma, Xia Yang, Qiaojiajie Zhao, Kuan Tan, Hong Chen, Deng Chen, Bing-Ren Huang.
Abstract
Transforming growth factor β (TGF-β), a cytokine, and its receptors play a vital role during normal embryogenesis, cell proliferation, differentiation, apoptosis and migration. Ran-binding protein in the microtubule-organizing center (RanBPM) serves as a scaffold protein that has been shown to interact with many other proteins, such as MET, Axl/Sky, TRAF6, IFNR, TrKA and TrkB in addition to p75NTR. In the current study, we have identified RanBPM as a novel binding partner of TβRI by yeast two-hybrid assay. The TβRI and RanBPM association was confirmed by co-immunoprecipitation and GST pull-down experiments. Additionally, expression of RanBPM abrogated the interaction between TβRI and TRAF6. Furthermore, RanBPM could depress TGF-β induced TRAF6 ubiquitination, subsequent NF-κB signaling pathway, and block TGF-β induced TβRI nuclear accumulation. Taken together, our results reveal that RanBPM may modulate TGF-β-mediated downstream signaling and biological functions.Entities:
Keywords: Interaction; MAP; NF-κB; Ran-binding protein in the microtubule-organizing center; RanBPM; TACE; TAK1; TGF-β; TGF-β type I receptor; TGF-β type II receptor; TNF-alpha converting enzyme; TRAF6; TβRI; TβRII; Ubiquitination; mitogen-activated protein; nuclear factor KB; transforming growth factor (TGF)-activated kinase 1; transforming growth factor β; tumor necrosis factor (TNF)-receptor-associated factor 6
Mesh:
Substances:
Year: 2013 PMID: 24103590 DOI: 10.1016/j.cellsig.2013.09.019
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315