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Ubiquitin E3 ligase Nedd4-1 acts as a downstream target of PI3K/PTEN-mTORC1 signaling to promote neurite growth
Author(s) -
HungEn Hsia,
Rohit Kumar,
Rossella Lucà,
Michiko Takeda,
Julien Courchet,
Jonathan Nakashima,
Shumin Wu,
Sandra Goebbels,
Wenlin An,
Britta J. Eickholt,
Franck Polleux,
Daniela Rotin,
Hong Wu,
Moritz J. Rossner,
Claudia Bagni,
JeongSeop Rhee,
Nils Brose,
Hiroshi Kawabe
Publication year - 2014
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1400737111
Subject(s) - nedd4 , pten , ubiquitin ligase , tensin , ubiquitin , biology , microbiology and biotechnology , neurite , mtorc1 , pi3k/akt/mtor pathway , signal transduction , biochemistry , gene , in vitro
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.

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