Evidence map›Paper›PMID 34849872›Full record

ArticleGenetics2022

A role for the Erk MAPK pathway in modulating SAX-7/L1CAM-dependent locomotion in Caenorhabditis elegans.

Melinda Moseley-Alldredge, Seema Sheoran, Hayoung Yoo, Calvin O'Keefe, Janet E Richmond, Lihsia Chen

Open access · greenAbstract read
In one paragraph

Article in Genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. 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.

Melinda Moseley-AlldredgeDepartment of Genetics, Cell Biology & Development, University of Minnesota, Minneapolis, MN 55455, USA.
Seema SheoranDepartment of Biological Sciences, University of Illinois, Chicago, IL 60607, USA.ORCID 0000-0003-0227-856X
Hayoung YooDepartment of Genetics, Cell Biology & Development, University of Minnesota, Minneapolis, MN 55455, USA.
Calvin O'KeefeDepartment of Genetics, Cell Biology & Development, University of Minnesota, Minneapolis, MN 55455, USA.
Janet E RichmondDepartment of Biological Sciences, University of Illinois, Chicago, IL 60607, USA.
Lihsia ChenDepartment of Genetics, Cell Biology & Development, University of Minnesota, Minneapolis, MN 55455, USA.ORCID 0000-0003-2386-7734
University of Minnesota · USUniversity of Illinois Chicago · US

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
L1CAM Adhesion and Signaling Pathways in C. elegansR01NS045873 · NINDS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CHEN, LIHSIA · 2005 to 2021
$3.9M
NIH HHS P40 OD010440NINDS NIH HHS R01 NS045873
6 · The paper itself

Abstract

L1CAMs are immunoglobulin cell adhesion molecules that function in nervous system development and function. Besides being associated with autism and schizophrenia spectrum disorders, impaired L1CAM function also underlies the X-linked L1 syndrome, which encompasses a group of neurological conditions, including spastic paraplegia and congenital hydrocephalus. Studies on vertebrate and invertebrate L1CAMs established conserved roles that include axon guidance, dendrite morphogenesis, synapse development, and maintenance of neural architecture. We previously identified a genetic interaction between the Caenorhabditis elegans L1CAM encoded by the sax-7 gene and RAB-3, a GTPase that functions in synaptic neurotransmission; rab-3; sax-7 mutant animals exhibit synthetic locomotion abnormalities and neuronal dysfunction. Here, we show that this synergism also occurs when loss of SAX-7 is combined with mutants of other genes encoding key players of the synaptic vesicle (SV) cycle. In contrast, sax-7 does not interact with genes that function in synaptogenesis. These findings suggest a postdevelopmental role for sax-7 in the regulation of synaptic activity. To assess this possibility, we conducted electrophysiological recordings and ultrastructural analyses at neuromuscular junctions; these analyses did not reveal obvious synaptic abnormalities. Lastly, based on a forward genetic screen for suppressors of the rab-3; sax-7 synthetic phenotypes, we determined that mutants in the ERK Mitogen-activated Protein Kinase (MAPK) pathway can suppress the rab-3; sax-7 locomotion defects. Moreover, we established that Erk signaling acts in a subset of cholinergic neurons in the head to promote coordinated locomotion. In combination, these results suggest a modulatory role for Erk MAPK in L1CAM-dependent locomotion in C. elegans.

Indexed as

Caenorhabditis elegans ProteinsNeural Cell Adhesion Molecule L1AnimalsCaenorhabditis elegansCholinergic NeuronsLocomotionMitogen-Activated Protein KinasesMutationNeural Cell Adhesion MoleculesCaenorhabditis elegans ProteinsMitogen-Activated Protein KinasesNeural Cell Adhesion Molecule L1Neural Cell Adhesion MoleculesSAX-7 protein, C elegansC. elegansKSR-1MAPKsax-7 L1CAMsynaptic regulation

Identifiers

PMID34849872
PMCPMC9097276
OpenAlexW3215479900

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.