RBX2 maintains final retinal cell position in a DAB1-dependent and -independent fashion

Corinne L. Fairchild, Keiko Hino, Jisoo S. Han, Adam M. Miltner, Gabriel Peinado Allina, Caileigh E. Brown, Marie E Burns, Anna La Torre Vila, Sergi Simo Olivar

Research output: Contribution to journalArticlepeer-review

7 Scopus citations


The laminated structure of the retina is fundamental for the organization of the synaptic circuitry that translates light input into patterns of action potentials. However, the molecular mechanisms underlying cell migration and layering of the retina are poorly understood. Here, we show that RBX2, a core component of the E3 ubiquitin ligase CRL5, is essential for retinal layering and function. RBX2 regulates the final cell position of rod bipolar cells, cone photoreceptors and Muller glia. Our data indicate that sustained RELN/DAB1 signaling, triggered by depletion of RBX2 or SOCS7 – a CRL5 substrate adaptor known to recruit DAB1 – causes rod bipolar cell misposition. Moreover, whereas SOCS7 also controls Muller glia cell lamination, it is not responsible for cone photoreceptor positioning, suggesting that RBX2, most likely through CRL5 activity, controls other signaling pathways required for proper cone localization. Furthermore, RBX2 depletion reduces the number of ribbon synapses and disrupts cone photoreceptor function. Together, these results uncover RBX2 as a crucial molecular regulator of retina morphogenesis and cone photoreceptor function.

Original languageEnglish (US)
Article numberdev155283
JournalDevelopment (Cambridge)
Issue number3
StatePublished - Feb 1 2018


  • CRL5
  • DAB1
  • Neuron migration
  • RBX2
  • Retina development

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology


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