The Centrosomal E3 Ubiquitin Ligase FBXO31-SCF Regulates Neuronal Morphogenesis and Migration

2013-02-28 | journal article. A publication with affiliation to the University of Göttingen.

Jump to: Cite & Linked | Documents & Media | Details | Version history

Cite this publication

​The Centrosomal E3 Ubiquitin Ligase FBXO31-SCF Regulates Neuronal Morphogenesis and Migration​
Vadhvani, M.; Schwedhelm-Domeyer, N.; Mukherjee, C. & Stegmüller, J.​ (2013) 
PLoS ONE8(2) art. e57530​.​ DOI: https://doi.org/10.1371/journal.pone.0057530 

Documents & Media

journal.pone.0057530.pdf2.29 MBAdobe PDF

License

Published Version

Attribution 3.0 CC BY 3.0

Details

Authors
Vadhvani, Mayur; Schwedhelm-Domeyer, Nicola; Mukherjee, Chaitali; Stegmüller, Judith
Abstract
Neuronal development requires proper migration, polarization and establishment of axons and dendrites. Growing evidence identifies the ubiquitin proteasome system (UPS) with its numerous components as an important regulator of various aspects of neuronal development. F-box proteins are interchangeable subunits of the Cullin-1 based E3 ubiquitin ligase, but only a few family members have been studied. Here, we report that the centrosomal E3 ligase FBXO31-SCF (Skp1/ Cullin-1/F-box protein) regulates neuronal morphogenesis and axonal identity. In addition, we identified the polarity protein Par6c as a novel interaction partner and substrate targeted for proteasomal degradation in the control of axon but not dendrite growth. Finally, we ascribe a role for FBXO31 in dendrite growth and neuronal migration in the developing cerebellar cortex. Taken together, we uncovered the centrosomal E3 ligase FBXO31-SCF as a novel regulator of neuronal development.
Issue Date
28-February-2013
Journal
PLoS ONE 
ISSN
1932-6203
Extent
13
Language
English

Reference

Citations


Social Media