Evidence map›Paper›PMID 36573271›Full record

ArticleGenetics2023

wrk-1 and rig-5 control pioneer and follower axon navigation in the ventral nerve cord of Caenorhabditis elegans in a nid-1 mutant background.

Abigail H Feresten, Jaffar M Bhat, Alex J Yu, Richard Zapf, Catharine H Rankin, Harald Hutter

Open access · greenAbstract read
In one paragraph

Article in Genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Neuropeptides Involved in Elicited Reversal Speed Plasticity inbioRxiv : the preprint server for biology · 2025
    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

6 authors at 2 institutions in 1 country.

Abigail H FerestenDepartment of Biological Sciences, and Center for Cell Biology, Development, and Disease, Simon Fraser University, Burnaby, BC V5A1S6, Canada.
Jaffar M BhatDepartment of Biological Sciences, and Center for Cell Biology, Development, and Disease, Simon Fraser University, Burnaby, BC V5A1S6, Canada.
Alex J YuDjavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, BC V6T2B5, Canada.
Richard ZapfDepartment of Biological Sciences, and Center for Cell Biology, Development, and Disease, Simon Fraser University, Burnaby, BC V5A1S6, Canada.
Catharine H RankinDjavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, BC V6T2B5, Canada.
Harald HutterDepartment of Biological Sciences, and Center for Cell Biology, Development, and Disease, Simon Fraser University, Burnaby, BC V5A1S6, Canada.
Simon Fraser University · CAUniversity of British Columbia · CA

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

During nervous system development, neurons send out axons, which must navigate large distances to reach synaptic targets. Axons grow out sequentially. The early outgrowing axons, pioneers, must integrate information from various guidance cues in their environment to determine the correct direction of outgrowth. Later outgrowing follower axons can at least in part navigate by adhering to pioneer axons. In Caenorhabditis elegans, the right side of the largest longitudinal axon tract, the ventral nerve cord, is pioneered by the AVG axon. How the AVG axon navigates is only partially understood. In this study, we describe the role of two members of the IgCAM family, wrk-1 and rig-5, in AVG axon navigation. While wrk-1 and rig-5 single mutants do not show AVG navigation defects, both mutants have highly penetrant pioneer and follower navigation defects in a nid-1 mutant background. Both mutations increase the fraction of follower axons following the misguided pioneer axon. We found that wrk-1 and rig-5 act in different genetic pathways, suggesting that we identified two pioneer-independent guidance pathways used by follower axons. We assessed general locomotion, mechanosensory responsiveness, and habituation to determine whether axonal navigation defects impact nervous system function. In rig-5 nid-1 double mutants, we found no significant defects in free movement behavior; however, a subpopulation of animals shows minor changes in response duration habituation after mechanosensory stimulation. These results suggest that guidance defects of axons in the motor circuit do not necessarily lead to major movement or behavioral defects but impact more complex behavioral modulation.

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsAnimalsAxonsCalcium-Binding ProteinsExtracellular Matrix ProteinsMutationNerve Tissue ProteinsNeuronsCaenorhabditis elegans ProteinsCalcium-Binding ProteinsExtracellular Matrix ProteinsNerve Tissue Proteinsnid-1 protein, C elegansrig-5 protein, C elegansWRK-1 protein, C elegansaxon guidanceaxon navigationhabituationIgCAMnervous system developmentpioneer

Identifiers

PMID36573271
PMCPMC9991498
OpenAlexW4312210037

What OpenQuestion holds

Textmetadata
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.