| Literature DB >> 25143387 |
Fu-Zon Chung1, Anagh A Sahasrabuddhe1, Kaiyu Ma1, Xiaofei Chen1, Venkatesha Basrur1, Megan S Lim2, Kojo S J Elenitoba-Johnson3.
Abstract
Fbxo45 is an atypical E3 ubiquitin ligase, which specifically targets proteins for ubiquitin-mediated degradation. Fbxo45 ablation results in defective neuronal differentiation and abnormal formation of neural connections; however, the mechanisms underlying these defects are poorly understood. Using an unbiased mass spectrometry-based proteomic screen, we show here that N-cadherin is a novel interactor of Fbxo45. N-cadherin specifically interacts with Fbxo45 through two consensus motifs overlapping the site of calcium-binding and dimerization of the cadherin molecule. N-cadherin interaction with Fbxo45 is significantly abrogated by calcium treatment. Surprisingly, Fbxo45 depletion by RNAi-mediated silencing results in enhanced proteolysis of N-cadherin. Conversely, ectopic expression of Fbxo45 results in decreased proteolysis of N-cadherin. Fbxo45 depletion results in dramatic reduction in N-cadherin expression, impaired neuronal differentiation, and diminished formation of neuronal processes. Our studies reveal an unanticipated role for an F-box protein that inhibits proteolysis in the regulation of a critical biological process.Entities:
Keywords: Calcium; Cell Differentiation; Endocytosis; Intramembrane Proteolysis; Plasma Membrane
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Year: 2014 PMID: 25143387 PMCID: PMC4192496 DOI: 10.1074/jbc.M114.561241
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157