| Literature DB >> 25157163 |
Hung-En Hsia1, Rohit Kumar1, Rossella Luca2, Michiko Takeda1, Julien Courchet3, Jonathan Nakashima4, Shumin Wu4, Sandra Goebbels5, Wenlin An6, Britta J Eickholt6, Franck Polleux3, Daniela Rotin7, Hong Wu4, Moritz J Rossner8, Claudia Bagni9, Jeong-Seop Rhee1, Nils Brose1, Hiroshi Kawabe10.
Abstract
Protein ubiquitination is a core regulatory determinant of neural development. Previous studies have indicated that the Nedd4-family E3 ubiquitin ligases Nedd4-1 and Nedd4-2 may ubiquitinate phosphatase and tensin homolog (PTEN) and thereby regulate axonal growth in neurons. Using conditional knockout mice, we show here that Nedd4-1 and Nedd4-2 are indeed required for axonal growth in murine central nervous system neurons. However, in contrast to previously published data, we demonstrate that PTEN is not a substrate of Nedd4-1 and Nedd4-2, and that aberrant PTEN ubiquitination is not involved in the impaired axon growth upon deletion of Nedd4-1 and Nedd4-2. Rather, PTEN limits Nedd4-1 protein levels by modulating the activity of mTORC1, a protein complex that controls protein synthesis and cell growth. Our data demonstrate that Nedd4-family E3 ligases promote axonal growth and branching in the developing mammalian brain, where PTEN is not a relevant substrate. Instead, PTEN controls neurite growth by regulating Nedd4-1 expression.Entities:
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Year: 2014 PMID: 25157163 PMCID: PMC4246980 DOI: 10.1073/pnas.1400737111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205