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.

Hsia, H., Kumar, R., Luca, R., Takeda, M., Courchet, J., Nakashima, J., et al. (2014). Ubiquitin E3 ligase Nedd4-1 acts as a downstream target of PI3K/PTEN-mTORC1 signaling to promote neurite growth. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 111(36), 13205-13210 [10.1073/pnas.1400737111].

Ubiquitin E3 ligase Nedd4-1 acts as a downstream target of PI3K/PTEN-mTORC1 signaling to promote neurite growth

BAGNI, CLAUDIA
Membro del Collaboration Group
;
2014-01-01

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.
2014
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/13 - BIOLOGIA APPLICATA
English
Animals; Axons; Cerebral Cortex; Endosomal Sorting Complexes Required for Transport; Hippocampus; Mice, Knockout; Models, Biological; Morphogenesis; Multiprotein Complexes; Neurites; PTEN Phosphohydrolase; Phosphatidylinositol 3-Kinases; Polyubiquitin; Protein Biosynthesis; TOR Serine-Threonine Kinases; Ubiquitin-Protein Ligases; Ubiquitination; Signal Transduction
Hsia, H., Kumar, R., Luca, R., Takeda, M., Courchet, J., Nakashima, J., et al. (2014). Ubiquitin E3 ligase Nedd4-1 acts as a downstream target of PI3K/PTEN-mTORC1 signaling to promote neurite growth. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 111(36), 13205-13210 [10.1073/pnas.1400737111].
Hsia, H; Kumar, R; Luca, R; Takeda, M; Courchet, J; Nakashima, J; Wu, S; Goebbels, S; An, W; Eickholt, B; Polleux, F; Rotin, D; Wu, H; Rossner, M; Bagni, C; Rhee, J; Brose, N; Kawabe, H
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/244785
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