Evidence map›Paper›PMID 27223328›Full record

ArticleeLife2016

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

Janelle C Leggere, Yuhki Saito, Robert B Darnell, Marc Tessier-Lavigne, Harald J Junge, Zhe Chen

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.5field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 66 citations in OpenAlex.

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  12. NOVA2 regulates neural circRNA biogenesis.Nucleic acids research · 2021
    Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Alternative splicing programming of axon formation.Wiley interdisciplinary reviews. RNA · 2020
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Janelle C LeggereDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, United States.
Yuhki SaitoLaboratory of Molecular Neuro-Oncology, Howard Hughes Medical Institute, The Rockefeller University, New York, United States.
Robert B DarnellLaboratory of Molecular Neuro-Oncology, Howard Hughes Medical Institute, The Rockefeller University, New York, United States.ORCID 0000-0002-5134-8088
Marc Tessier-LavigneLaboratory of Brain Development and Repair, The Rockefeller University, New York, United States.
Harald J JungeDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, United States.
Zhe ChenDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, United States.ORCID 0000-0003-0683-9491
University of Colorado Boulder · USHoward Hughes Medical Institute · USRockefeller University · US

Funding

NEUROLOGY AND THE MOLECULAR ROLE OF N-RBPS IN THE BRAINR01NS034389 · NINDS · ROCKEFELLER UNIVERSITY · PI DARNELL, ROBERT B · 1995 to 2016
$6.3M
Mapping the mechanisms of protein synthesis-dependent synaptic plasticityR01NS081706 · NINDS · ROCKEFELLER UNIVERSITY · PI DARNELL, ROBERT B · 2012 to 2016
$5.3M
Norrin Signaling in the Retina: Regulation of the Blood-Retina BarrierR01EY024261 · NEI · UNIVERSITY OF MINNESOTA · PI Harald Junge · 2014 to 2026
$4.7M
RNA Dysregulation in ALSRC2NS069473 · NINDS · ROCKEFELLER UNIVERSITY · PI DARNELL, ROBERT B · 2009 to 2010
$1000k
NEI NIH HHS R01 EY024261NINDS NIH HHS R01 NS034389NINDS NIH HHS R01 NS081706NINDS NIH HHS RC2 NS069473
6 · The paper itself

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.

Indexed as

Alternative SplicingAxon GuidanceGene Expression Regulation, DevelopmentalAnimalsAntigens, NeoplasmCommissural InterneuronsDCC ReceptorGenetic TestingMiceMice, KnockoutNeuro-Oncological Ventral AntigenRNA-Binding ProteinsRNA InterferenceSpinal CordAntigens, NeoplasmDcc protein, mouseDCC ReceptorNeuro-Oncological Ventral AntigenNova1 protein, mouseNova2 protein, mouseRNA-Binding Proteinsalternative splicingaxon guidanceDCCdevelopmental biologymouseneuronal migrationneuroscienceNOVARNA binding proteinsstem cells

Identifiers

PMID27223328
PMCPMC4930329
OpenAlexW2395185061

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.