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NOVA2-mediated RNA regulation is required for axonal pathfinding during development

The neuron specific RNA-binding proteins NOVA1 and NOVA2 are highly homologous alternative splicing regulators. NOVA proteins regulate at least 700 alternative splicing events in vivo, yet relatively little is known about the biologic consequences of NOVA action and in particular about functional di...

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Autores principales: Saito, Yuhki, Miranda-Rottmann, Soledad, Ruggiu, Matteo, Park, Christopher Y, Fak, John J, Zhong, Ru, Duncan, Jeremy S, Fabella, Brian A, Junge, Harald J, Chen, Zhe, Araya, Roberto, Fritzsch, Bernd, Hudspeth, A J, Darnell, Robert B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930328/
https://www.ncbi.nlm.nih.gov/pubmed/27223325
http://dx.doi.org/10.7554/eLife.14371
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author Saito, Yuhki
Miranda-Rottmann, Soledad
Ruggiu, Matteo
Park, Christopher Y
Fak, John J
Zhong, Ru
Duncan, Jeremy S
Fabella, Brian A
Junge, Harald J
Chen, Zhe
Araya, Roberto
Fritzsch, Bernd
Hudspeth, A J
Darnell, Robert B
author_facet Saito, Yuhki
Miranda-Rottmann, Soledad
Ruggiu, Matteo
Park, Christopher Y
Fak, John J
Zhong, Ru
Duncan, Jeremy S
Fabella, Brian A
Junge, Harald J
Chen, Zhe
Araya, Roberto
Fritzsch, Bernd
Hudspeth, A J
Darnell, Robert B
author_sort Saito, Yuhki
collection PubMed
description The neuron specific RNA-binding proteins NOVA1 and NOVA2 are highly homologous alternative splicing regulators. NOVA proteins regulate at least 700 alternative splicing events in vivo, yet relatively little is known about the biologic consequences of NOVA action and in particular about functional differences between NOVA1 and NOVA2. Transcriptome-wide searches for isoform-specific functions, using NOVA1 and NOVA2 specific HITS-CLIP and RNA-seq data from mouse cortex lacking either NOVA isoform, reveals that NOVA2 uniquely regulates alternative splicing events of a series of axon guidance related genes during cortical development. Corresponding axonal pathfinding defects were specific to NOVA2 deficiency: Nova2-/- but not Nova1-/- mice had agenesis of the corpus callosum, and axonal outgrowth defects specific to ventral motoneuron axons and efferent innervation of the cochlea. Thus we have discovered that NOVA2 uniquely regulates alternative splicing of a coordinate set of transcripts encoding key components in cortical, brainstem and spinal axon guidance/outgrowth pathways during neural differentiation, with severe functional consequences in vivo. DOI: http://dx.doi.org/10.7554/eLife.14371.001
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spelling pubmed-49303282016-07-05 NOVA2-mediated RNA regulation is required for axonal pathfinding during development Saito, Yuhki Miranda-Rottmann, Soledad Ruggiu, Matteo Park, Christopher Y Fak, John J Zhong, Ru Duncan, Jeremy S Fabella, Brian A Junge, Harald J Chen, Zhe Araya, Roberto Fritzsch, Bernd Hudspeth, A J Darnell, Robert B eLife Neuroscience The neuron specific RNA-binding proteins NOVA1 and NOVA2 are highly homologous alternative splicing regulators. NOVA proteins regulate at least 700 alternative splicing events in vivo, yet relatively little is known about the biologic consequences of NOVA action and in particular about functional differences between NOVA1 and NOVA2. Transcriptome-wide searches for isoform-specific functions, using NOVA1 and NOVA2 specific HITS-CLIP and RNA-seq data from mouse cortex lacking either NOVA isoform, reveals that NOVA2 uniquely regulates alternative splicing events of a series of axon guidance related genes during cortical development. Corresponding axonal pathfinding defects were specific to NOVA2 deficiency: Nova2-/- but not Nova1-/- mice had agenesis of the corpus callosum, and axonal outgrowth defects specific to ventral motoneuron axons and efferent innervation of the cochlea. Thus we have discovered that NOVA2 uniquely regulates alternative splicing of a coordinate set of transcripts encoding key components in cortical, brainstem and spinal axon guidance/outgrowth pathways during neural differentiation, with severe functional consequences in vivo. DOI: http://dx.doi.org/10.7554/eLife.14371.001 eLife Sciences Publications, Ltd 2016-05-25 /pmc/articles/PMC4930328/ /pubmed/27223325 http://dx.doi.org/10.7554/eLife.14371 Text en © 2016, Saito et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Saito, Yuhki
Miranda-Rottmann, Soledad
Ruggiu, Matteo
Park, Christopher Y
Fak, John J
Zhong, Ru
Duncan, Jeremy S
Fabella, Brian A
Junge, Harald J
Chen, Zhe
Araya, Roberto
Fritzsch, Bernd
Hudspeth, A J
Darnell, Robert B
NOVA2-mediated RNA regulation is required for axonal pathfinding during development
title NOVA2-mediated RNA regulation is required for axonal pathfinding during development
title_full NOVA2-mediated RNA regulation is required for axonal pathfinding during development
title_fullStr NOVA2-mediated RNA regulation is required for axonal pathfinding during development
title_full_unstemmed NOVA2-mediated RNA regulation is required for axonal pathfinding during development
title_short NOVA2-mediated RNA regulation is required for axonal pathfinding during development
title_sort nova2-mediated rna regulation is required for axonal pathfinding during development
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930328/
https://www.ncbi.nlm.nih.gov/pubmed/27223325
http://dx.doi.org/10.7554/eLife.14371
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