Evidence map›Paper›PMID 22855524›Full record

ArticleMolecular biology of the cell2012

The kinesin-3 family motor KLP-4 regulates anterograde trafficking of GLR-1 glutamate receptors in the ventral nerve cord of Caenorhabditis elegans.

Michael I Monteiro, Shikha Ahlawat, Jennifer R Kowalski, Emily Malkin, Sandhya P Koushika, Peter Juo

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Kinesins inOpen biology · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Reactive Oxygen Species Modulate Activity-Dependent AMPA Receptor Transport inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  9. LDL receptor related protein 1 requires the IBiochimica et biophysica acta. Molecular cell research · 2019
    Article
  10. KIF2A characterization after spinal cord injury.Cellular and molecular life sciences : CMLS · 2019
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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.

Michael I MonteiroDepartment of Molecular Physiology and Pharmacology, Tufts University School of Medicine, Boston, MA 02111, USA.
Shikha Ahlawat
Jennifer R Kowalski
Emily Malkin
Sandhya P Koushika
Peter Juo

Funding

TUSM/T-NEMC CENTER FOR NEUROSCIENCE RESEARCH - Imaging CoreP30NS047243 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2003 to 2017
$10.0M
Training in Education and Critical Research SkillsK12GM074869 · NIGMS · TUFTS UNIVERSITY BOSTON · PI MOORE, CLAIRE L · 2006 to 2017
$8.5M
Molecular and genetic analysis of CDK-5 function in synaptic transmissionR01NS059953 · NINDS · TUFTS UNIVERSITY BOSTON · PI JUO, PETER C · 2007 to 2011
$1.8M
Physician & Scientist Training in Developmental GeneticsT32HD049341 · NICHD · TUFTS MEDICAL CENTER · PI BIANCHI, DIANA W. · 2006 to 2010
$1.4M
Molecular and genetic analysis of CDK-5 function in synaptic transmissionR56NS059953 · NINDS · TUFTS UNIVERSITY BOSTON · PI JUO, PETER C · 2013 to 2013
$413k
NICHD NIH HHS T32 HD 049341NICHD NIH HHS T32 HD049341NIGMS NIH HHS 5K12GM074869NIGMS NIH HHS K12 GM074869NINDS NIH HHS NS059953NINDS NIH HHS P30 NS 047243NINDS NIH HHS P30 NS047243NINDS NIH HHS R01 NS059953NINDS NIH HHS R56 NS059953
6 · The paper itself

Abstract

The transport of glutamate receptors from the cell body to synapses is essential during neuronal development and may contribute to the regulation of synaptic strength in the mature nervous system. We previously showed that cyclin-dependent kinase-5 (CDK-5) positively regulates the abundance of GLR-1 glutamate receptors at synapses in the ventral nerve cord (VNC) of Caenorhabditis elegans. Here we identify a kinesin-3 family motor klp-4/KIF13 in a cdk-5 suppressor screen for genes that regulate GLR-1 trafficking. klp-4 mutants have decreased abundance of GLR-1 in the VNC. Genetic analysis of klp-4 and the clathrin adaptin unc-11/AP180 suggests that klp-4 functions before endocytosis in the ventral cord. Time-lapse microscopy indicates that klp-4 mutants exhibit decreased anterograde flux of GLR-1. Genetic analysis of cdk-5 and klp-4 suggests that they function in the same pathway to regulate GLR-1 in the VNC. Interestingly, GLR-1 accumulates in cell bodies of cdk-5 but not klp-4 mutants. However, GLR-1 does accumulate in klp-4-mutant cell bodies if receptor degradation in the multivesicular body/lysosome pathway is blocked. This study identifies kinesin KLP-4 as a novel regulator of anterograde glutamate receptor trafficking and reveals a cellular control mechanism by which receptor cargo is targeted for degradation in the absence of its motor.

Indexed as

Amino Acid SequenceAnimalsAnimals, Genetically ModifiedCaenorhabditis elegansCaenorhabditis elegans ProteinsCyclin-Dependent Kinase 5EndocytosisGreen Fluorescent ProteinsInterneuronsKinesinsLysosomesMicroscopy, FluorescenceMolecular Sequence DataMultivesicular BodiesMutationNerve Tissue ProteinsCaenorhabditis elegans ProteinsCyclin-Dependent Kinase 5glr-1 protein, C elegansGreen Fluorescent ProteinsKinesinsKLP-4 protein, C elegansNerve Tissue ProteinsReceptors, AMPAunc-11 protein, C elegans

Identifiers

PMID22855524
PMCPMC3442412

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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.