Evidence map›Paper›PMID 31969659›Full record

ArticleScientific reports2020

Onecut-dependent Nkx6.2 transcription factor expression is required for proper formation and activity of spinal locomotor circuits.

Mathilde Toch, Audrey Harris, Olivier Schakman, Elena Kondratskaya, Jean-Luc Boulland, Nicolas Dauguet, Stéphanie Debrulle, Charlotte Baudouin, Maria Hidalgo-Figueroa, Xiuqian Mu and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 4 countries.

Mathilde TochUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Neural Differentiation, Brussels, Belgium.
Audrey HarrisUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Neural Differentiation, Brussels, Belgium.
Olivier SchakmanUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Cell Physiology, Brussels, Belgium.ORCID http://orcid.org/0000-0001-6440-0327
Elena KondratskayaLaboratory for Neural Development and Optical Recording (NDEVOR), Section for Physiology, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Jean-Luc BoullandNorwegian Center for Stem Cell Research, Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0002-7272-357X
Nicolas DauguetUniversité catholique de Louvain, de Duve Institute, Flow cytometry and cell sorting facility (CYTF), Brussels, Belgium.
Stéphanie DebrulleUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Neural Differentiation, Brussels, Belgium.
Charlotte BaudouinUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Neural Differentiation, Brussels, Belgium.
Maria Hidalgo-FigueroaUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Neural Differentiation, Brussels, Belgium.
Xiuqian MuDepartment of Ophthalmology/Ross Eye Institute, New York State Center of Excellence in Bioinformatics and Life Sciences, University at Buffalo, Buffalo, NY, 14203, USA.
Alexander GowWayne state University, Center for Molecular Medicine and Genetics, Carman and Ann Adams Department of Pediatrics, Department of Neurology, Detroit, Michigan, USA.ORCID http://orcid.org/0000-0001-7446-8990
Joel C GloverLaboratory for Neural Development and Optical Recording (NDEVOR), Section for Physiology, Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Fadel TissirUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Developmental Neurobiology, Brussels, Belgium.ORCID http://orcid.org/0000-0002-9292-6622
Frédéric ClotmanUniversité catholique de Louvain, Institute of Neuroscience, Laboratory of Neural Differentiation, Brussels, Belgium. frederic.clotman@uclouvain.be.
UCLouvain · BEOslo University Hospital · NOde Duve Institute · BEUniversidad de Cádiz · ESUniversity of Oslo · NOWayne State University · US

Funding

Regulation of mRNA decay in retinal development and maintenanceR01EY029705 · NEI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MU, XIUQIAN · 2020 to 2023
$2.0M
Characterizing the radial component of CNS myelinR21NS102678 · NINDS · WAYNE STATE UNIVERSITY · PI GOW, ALEXANDER · 2017 to 2018
$424k
NEI NIH HHS R01 EY029705NINDS NIH HHS R21 NS102678
6 · The paper itself

Abstract

In the developing spinal cord, Onecut transcription factors control the diversification of motor neurons into distinct neuronal subsets by ensuring the maintenance of Isl1 expression during differentiation. However, other genes downstream of the Onecut proteins and involved in motor neuron diversification have remained unidentified. In the present study, we generated conditional mutant embryos carrying specific inactivation of Onecut genes in the developing motor neurons, performed RNA-sequencing to identify factors downstream of Onecut proteins in this neuron population, and employed additional transgenic mouse models to assess the role of one specific Onecut-downstream target, the transcription factor Nkx6.2. Nkx6.2 expression was up-regulated in Onecut-deficient motor neurons, but strongly downregulated in Onecut-deficient V2a interneurons, indicating an opposite regulation of Nkx6.2 by Onecut factors in distinct spinal neuron populations. Nkx6.2-null embryos, neonates and adult mice exhibited alterations of locomotor pattern and spinal locomotor network activity, likely resulting from defective survival of a subset of limb-innervating motor neurons and abnormal migration of V2a interneurons. Taken together, our results indicate that Nkx6.2 regulates the development of spinal neuronal populations and the formation of the spinal locomotor circuits downstream of the Onecut transcription factors.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsGene ExpressionHomeodomain ProteinsLocomotionMiceMice, TransgenicMotor NeuronsOnecut Transcription FactorsSpinal CordTranscription FactorsHomeodomain ProteinsNkx6-2 protein, mouseOnecut Transcription FactorsTranscription Factors

Identifiers

PMID31969659
PMCPMC6976625
OpenAlexW3002573271

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.