Evidence map›Paper›PMID 26818503›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Equivalent Activities of Repulsive Axon Guidance Receptors.

Hong Long, Shingo Yoshikawa, John B Thomas

Open access · hybridAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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

3 authors at 1 institution in 1 country.

Hong LongMolecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037.
Shingo YoshikawaMolecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037.
John B ThomasMolecular Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037 jthomas@salk.edu.
Salk Institute for Biological Studies · US

Funding

AXON GUIDANCE MECHANISMS IN DROSOPHILAR01NS040963 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI THOMAS, JOHN B · 2001 to 2010
$4.4M
Regulation of Energy Balance in DrosophilaR01DK077979 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI THOMAS, JOHN B · 2009 to 2012
$1.4M
Regulation of satiety and energy balance in DrosophilaR56DK077979 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI THOMAS, JOHN B · 2008 to 2008
$144k
Canadian Institutes of Health ResearchNIDDK NIH HHS DK077979NIDDK NIH HHS R01 DK077979NIDDK NIH HHS R56 DK077979NINDS NIH HHS NS040963NINDS NIH HHS R01 NS040963
6 · The paper itself

Abstract

Receptors on the growth cone at the leading edge of elongating axons play critical guidance roles by recognizing cues via their extracellular domains and transducing signals via their intracellular domains, resulting in changes in direction of growth. An important concept to have emerged in the axon guidance field is the importance of repulsion as a major guidance mechanism. Given the number and variety of different repulsive receptors, it is generally thought that there are likely to be qualitative differences in the signals they transduce. However, the nature of these possible differences is unknown. By creating chimeras using the extracellular and intracellular domains of three different Drosophila repulsive receptors, Unc5, Roundabout (Robo), and Derailed (Drl) and expressing them in defined cells within the embryonic nervous system, we examined the responses elicited by their intracellular domains systematically. Surprisingly, we found no qualitative differences in growth cone response or axon growth, suggesting that, despite their highly diverged sequences, each intracellular domain elicits repulsion via a common pathway. In terms of the signaling pathway(s) used by the repulsive receptors, mutations in the guanine nucleotide exchange factor Trio strongly enhance the repulsive activity of all three intracellular domains, suggesting that repulsion by Unc5, Robo, and Drl, and perhaps repulsion in general, involves Trio activity. SIGNIFICANCE STATEMENT: A prevailing concept that has emerged in the axon guidance field is the importance of repulsion as a guidance mechanism for steering axons to their appropriate targets. Given the number and variety of different repulsive receptors, it is generally thought that there are differences in the signals that they transduce. However, this has never been tested directly. We have used the advanced genetics of Drosophila to compare directly the outputs of different repulsive receptors. Surprisingly, we found no qualitative differences in receptor-mediated repulsion, suggesting that, despite their highly diverged domain structure, each receptor couples to a common repulsive pathway. We went on to show that this common pathway involves Trio, a guanine nucleotide exchange factor known to promote cytoskeletal remodeling.

Indexed as

AnimalsAnimals, Genetically ModifiedAxonsDrosophilaDrosophila ProteinsEmbryo, NonmammalianGreen Fluorescent ProteinsGrowth ConesMutationNerve Tissue ProteinsNeuronsReceptor Protein-Tyrosine KinasesReceptors, ImmunologicRoundabout ProteinsSignal TransductionDRL protein, DrosophilaDrosophila ProteinsGreen Fluorescent ProteinsNerve Tissue ProteinsReceptor Protein-Tyrosine KinasesReceptors, ImmunologicRoundabout ProteinsUNC protein, Drosophilaaxon guidanceDrosophilagrowth conereceptorrepulsionTrio

Identifiers

PMID26818503
PMCPMC4728722
OpenAlexW2337840755

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.