Evidence map›Paper›PMID 26904955›Full record

ArticleCell reports2016

Hox Proteins Coordinate Motor Neuron Differentiation and Connectivity Programs through Ret/Gfrα Genes.

Catarina Catela, Maggie M Shin, David H Lee, Jeh-Ping Liu, Jeremy S Dasen

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.7field-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

43 citing papers in PubMed, 79 citations in OpenAlex.

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  3. TheiScience · 2025
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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

5 authors at 2 institutions in 1 country.

Catarina CatelaNeuroscience Institute, Department of Neuroscience and Physiology, NYU School of Medicine, New York, NY 10016, USA.
Maggie M ShinNeuroscience Institute, Department of Neuroscience and Physiology, NYU School of Medicine, New York, NY 10016, USA.
David H LeeNeuroscience Institute, Department of Neuroscience and Physiology, NYU School of Medicine, New York, NY 10016, USA.
Jeh-Ping LiuDepartment of Neuroscience, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
Jeremy S DasenNeuroscience Institute, Department of Neuroscience and Physiology, NYU School of Medicine, New York, NY 10016, USA. Electronic address: jeremy.dasen@nyumc.org.
Neurosciences Institute · USUniversity of Virginia · US

Funding

Transcriptional Control of Motor Neuron Identity and Connectivity. - Renewal - 1R01NS062822 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DASEN, JEREMY S · 2009 to 2019
$3.9M
Training Program in Molecular, Cellular, and Translational NeuroscienceT32NS086750 · NINDS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI JEREMY S DASEN, Katherine Nagel · 2014 to 2026
$2.4M
Control of Hox gene expression and neuronal identityR01NS045933 · NINDS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LIU, JEH-PING · 2003 to 2007
$1.6M
NINDS NIH HHS R01 NS045933NINDS NIH HHS R01 NS062822NINDS NIH HHS R01NS062822NINDS NIH HHS T32 NS086750NINDS NIH HHS T32NS086750
6 · The paper itself

Abstract

The accuracy of neural circuit assembly relies on the precise spatial and temporal control of synaptic specificity determinants during development. Hox transcription factors govern key aspects of motor neuron (MN) differentiation; however, the terminal effectors of their actions are largely unknown. We show that Hox/Hox cofactor interactions coordinate MN subtype diversification and connectivity through Ret/Gfrα receptor genes. Hox and Meis proteins determine the levels of Ret in MNs and define the intrasegmental profiles of Gfrα1 and Gfrα3 expression. Loss of Ret or Gfrα3 leads to MN specification and innervation defects similar to those observed in Hox mutants, while expression of Ret and Gfrα1 can bypass the requirement for Hox genes during MN pool differentiation. These studies indicate that Hox proteins contribute to neuronal fate and muscle connectivity through controlling the levels and pattern of cell surface receptor expression, consequently gating the ability of MNs to respond to limb-derived instructive cues.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DifferentiationChick EmbryoEmbryo, MammalianForelimbGlial Cell Line-Derived Neurotrophic Factor ReceptorsHomeodomain ProteinsMiceMotor NeuronsMuscle, SkeletalMutationMyeloid Ecotropic Viral Integration Site 1 ProteinNeoplasm ProteinsNeurogenesisPhosphoproteinsGfra1 protein, mouseGfra3 protein, mouseGlial Cell Line-Derived Neurotrophic Factor ReceptorsHomeodomain ProteinsHoxa5 protein, mouseMyeloid Ecotropic Viral Integration Site 1 ProteinNeoplasm ProteinsPhosphoproteinsProtein IsoformsProto-Oncogene Proteins c-retRet protein, mouseTranscription Factors

Identifiers

PMID26904955
PMCPMC4775310
OpenAlexW2287678585

What OpenQuestion holds

Textmetadata
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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.