Rbx2 Regulates Neuronal Migration through Different Cullin 5-RING Ligase Adaptors

Sergi Simo Olivar, Jonathan A. Cooper

Research output: Contribution to journalArticle

29 Scopus citations

Abstract

Morphogenesis requires the proper migration and positioning of different cell types in the embryo. Much more is known about how cells start and guide their migrations than about how they stop when they reach their destinations. Here we provide evidence that Rbx2, a subunit of the Cullin 5-RING E3 ubiquitin ligase (CRL5) complex, stops neocortical projection neurons at their target layers. Rbx2 mutation causes neocortical and cerebellar ectopias dependent on Dab1, a key signaling protein in the Reelin pathway. SOCS7, a CRL5 substrate adaptor protein, is also required for neocortical layering. SOCS7-CRL5 complexes stimulate the ubiquitylation and turnover of Dab1. SOCS7 is upregulated during projection neuron migration, and unscheduled SOCS7 expression stops migration prematurely. Cerebellar development requires Rbx2 but not SOCS7, pointing to the importance of other CRL5 adaptors. Our results suggest that CRL5 adaptor expression is spatiotemporally regulated to modulate Reelin signaling and ensure normal neuron positioning in the developing brain.

Original languageEnglish (US)
Pages (from-to)399-411
Number of pages13
JournalDevelopmental Cell
Volume27
Issue number4
DOIs
StatePublished - Nov 25 2013
Externally publishedYes

ASJC Scopus subject areas

  • Developmental Biology
  • Medicine(all)

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