NOVA regulates Dcc alternative splicing during neuronal migration and axon guidance in the spinal cord

Author:

Leggere Janelle C1,Saito Yuhki2,Darnell Robert B2ORCID,Tessier-Lavigne Marc3,Junge Harald J1,Chen Zhe1ORCID

Affiliation:

1. Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, United States

2. Laboratory of Molecular Neuro-Oncology, Howard Hughes Medical Institute, The Rockefeller University, New York, United States

3. Laboratory of Brain Development and Repair, The Rockefeller University, New York, United States

Abstract

RNA-binding proteins (RBPs) control multiple aspects of post-transcriptional gene regulation and function during various biological processes in the nervous system. To further reveal the functional significance of RBPs during neural development, we carried out an in vivo RNAi screen in the dorsal spinal cord interneurons, including the commissural neurons. We found that the NOVA family of RBPs play a key role in neuronal migration, axon outgrowth, and axon guidance. Interestingly, Nova mutants display similar defects as the knockout of the Dcc transmembrane receptor. We show here that Nova deficiency disrupts the alternative splicing of Dcc, and that restoring Dcc splicing in Nova knockouts is able to rescue the defects. Together, our results demonstrate that the production of DCC splice variants controlled by NOVA has a crucial function during many stages of commissural neuron development.

Funder

Japan Society for the Promotion of Science

National Institutes of Health

Howard Hughes Medical Institute

Boettcher Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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