Evidence map›Paper›PMID 31945343›Full record

ArticleDevelopmental biology2020

Long-term activity drives dendritic branch elaboration of a C. elegans sensory neuron.

Jesse A Cohn, Elizabeth R Cebul, Giulio Valperga, Lotti Brose, Mario de Bono, Maxwell G Heiman, Jonathan T Pierce

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. The PVD neuron has male-specific structure and mating function inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Nonapoptotic role of EGL-1 in exopher production and neuronal health inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. The URX oxygen-sensing neurons inmicroPublication biology · 2020
    Article
  9. Article
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

7 authors at 5 institutions in 2 countries.

Jesse A CohnInstitute for Cellular and Molecular Biology, Department of Neuroscience, The University of Texas at Austin, TX, USA.
Elizabeth R CebulDepartment of Genetics, Blavatnik Institute, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA.
Giulio ValpergaDivision of Cell Biology, Medical Research Council Laboratory of Molecular Biology, Cambridge, United Kingdom.
Lotti BroseInstitute for Cellular and Molecular Biology, Department of Neuroscience, The University of Texas at Austin, TX, USA.
Mario de BonoDivision of Cell Biology, Medical Research Council Laboratory of Molecular Biology, Cambridge, United Kingdom.
Maxwell G HeimanDepartment of Genetics, Blavatnik Institute, Harvard Medical School and Boston Children's Hospital, Boston, MA, USA.
Jonathan T PierceInstitute for Cellular and Molecular Biology, Department of Neuroscience, The University of Texas at Austin, TX, USA. Electronic address: jonps@austin.utexas.edu.
The University of Texas at Austin · USBoston VA Research Institute · USHarvard University · USMedical Research Council · GBMRC Laboratory of Molecular Biology · GB

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Development of Specific Neuron-Glia AttachmentsR01NS112343 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Maxwell Heiman · 2019 to 2026
$3.3M
High-speed opto-fluidics to screen entire nervous system in aging and diseaseR01AG041135 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI BEN-YAKAR, ADELA, PIERCE, JONATHAN THOMAS · 2011 to 2015
$2.8M
Synergistic patterned neurodegeneration by APP and APOE4RF1AG057355 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI PIERCE, JONATHAN THOMAS · 2017 to 2017
$1.9M
Formation of a neuron-glia contact at single-cell resolution in C. elegansF31NS103371 · NINDS · HARVARD MEDICAL SCHOOL · PI CEBUL, ELIZABETH ROSE · 2017 to 2018
$64k
Medical Research Council MC_U105178786NIA NIH HHS R01 AG041135NIA NIH HHS RF1 AG057355NIH HHS P40 OD010440NINDS NIH HHS F31 NS103371NINDS NIH HHS R01 NS112343
6 · The paper itself

Abstract

Neuronal activity often leads to alterations in gene expression and cellular architecture. The nematode Caenorhabditis elegans, owing to its compact translucent nervous system, is a powerful system in which to study conserved aspects of the development and plasticity of neuronal morphology. Here we focus on one pair of sensory neurons, termed URX, which the worm uses to sense and avoid high levels of environmental oxygen. Previous studies have reported that the URX neuron pair has variable branched endings at its dendritic sensory tip. By controlling oxygen levels and analyzing mutants, we found that these microtubule-rich branched endings grow over time as a consequence of neuronal activity in adulthood. We also find that the growth of these branches correlates with an increase in cellular sensitivity to particular ranges of oxygen that is observable in the behavior of older worms. Given the strengths of C. elegans as a model organism, URX may serve as a potent system for uncovering genes and mechanisms involved in activity-dependent morphological changes in neurons and possible adaptive changes in the aging nervous system.

Indexed as

AgingAnaerobiosisAnimalsCaenorhabditis elegansCell PlasticityDendritesNervous SystemOxygenSensory Receptor CellsOxygen

Identifiers

PMID31945343
PMCPMC7170766
OpenAlexW3000539171

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.