Evidence map›Paper›PMID 19244282›Full record

ArticleDevelopment (Cambridge, England)2009

C. elegans CARMIL negatively regulates UNC-73/Trio function during neuronal development.

Pamela J Vanderzalm, Amita Pandey, Michael E Hurwitz, Laird Bloom, H Robert Horvitz, Gian Garriga

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Epithelial morphogenesis, tubulogenesis and forces in organogenesis.Current topics in developmental biology · 2021
    Review
  6. Article
  7. Article
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  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Noncanonical Notch function in motor axon guidance is mediated by Rac GTPase and the GEF1 domain of Trio.Developmental dynamics : an official publication of the American Association of Anatomists · 2011
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Distinct roles for CARMIL isoforms in cell migration.Molecular biology of the cell · 2009
    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 3 institutions in 1 country.

Pamela J VanderzalmMolecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Amita Pandey
Michael E Hurwitz
Laird Bloom
H Robert Horvitz
Gian Garriga
University of California, Berkeley · USMassachusetts Institute of Technology · USHoward Hughes Medical Institute · US

Funding

Genetic Analysis of Nematode Egg Laying and Co-regulated Behavioral SystemsR01GM024663 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HORVITZ, H ROBERT · 1985 to 2025
$10.1M
Wnt regulation of C. elegans neuroblast and neuronal polarityR01NS032057 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI GARRIGA, GIAN · 1994 to 2020
$6.7M
Screening of Synthetic Lethality with C. elegans RbK08CA104890 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI HURWITZ, MICHAEL E · 2004 to 2008
$680k
GENETIC ANALYSIS OF NEMATODE EGG-LAYINGR37GM024663 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HORVITZ, H R · 1991 to 2000
$363k
Howard Hughes Medical InstituteNCI NIH HHS K08 CA-104890NCI NIH HHS K08 CA104890NIGMS NIH HHS GM24663NIGMS NIH HHS R01 GM024663NIGMS NIH HHS R37 GM024663NINDS NIH HHS NS32057NINDS NIH HHS R01 NS032057
6 · The paper itself

Abstract

Whereas many molecules that promote cell and axonal growth cone migrations have been identified, few are known to inhibit these processes. In genetic screens designed to identify molecules that negatively regulate such migrations, we identified CRML-1, the C. elegans homolog of CARMIL. Although mammalian CARMIL acts to promote the migration of glioblastoma cells, we found that CRML-1 acts as a negative regulator of neuronal cell and axon growth cone migrations. Genetic evidence indicates that CRML-1 regulates these migrations by inhibiting the Rac GEF activity of UNC-73, a homolog of the Rac and Rho GEF Trio. The antagonistic effects of CRML-1 and UNC-73 can control the direction of growth cone migration by regulating the levels of the SAX-3 (a Robo homolog) guidance receptor. Consistent with the hypothesis that CRML-1 negatively regulates UNC-73 activity, these two proteins form a complex in vivo. Based on these observations, we propose a role for CRML-1 as a novel regulator of cell and axon migrations that acts through inhibition of Rac signaling.

Indexed as

Amino Acid SequenceAnimalsAnimals, Genetically ModifiedBase SequenceCaenorhabditis elegansCaenorhabditis elegans ProteinsCell MovementCloning, MolecularDNA PrimersDown-RegulationGene Expression Regulation, DevelopmentalGenes, HelminthModels, NeurologicalMolecular Sequence DataMutationNerve Tissue ProteinsCaenorhabditis elegans Proteinscrml-1 protein, C elegansDNA PrimersNerve Tissue Proteinsrac GTP-Binding ProteinsReceptors, ImmunologicRoundabout ProteinsUNC-73 protein, C elegans

Identifiers

PMID19244282
PMCPMC2685937
OpenAlexW2117170566

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.