Evidence map›Paper›PMID 15296748›Full record

ArticleCurrent biology : CB2004

Roundabout 2 regulates migration of sensory neurons by signaling in trans.

Rachel Kraut, Kai Zinn

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Current biology : CB, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
0.5field-weighted citation impact, top 46% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
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  7. Review
  8. Slit/Robo Signaling Regulates Multiple Stages of the Development of theFrontiers in cell and developmental biology · 2021
    Article
  9. Article
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  11. G3 (Bethesda, Md.) · 2018
    Article
  12. Article
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  15. Article
  16. Article
  17. Article
  18. Article
  19. Slits affect the timely migration of neural crest cells via Robo receptor.Developmental dynamics : an official publication of the American Association of Anatomists · 2012
    Article
  20. Roundabout is required in the visceral mesoderm for proper microvillus length in the hindgut epithelium.Developmental dynamics : an official publication of the American Association of Anatomists · 2012
    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

2 authors at 1 institution in 1 country.

Rachel KrautDivision of Biology 114-96, California Institute of Technology, Pasadena, CA 91125, USA.
Kai Zinn
California Institute of Technology · US

Funding

MOLECULAR GENETICS OF DROSOPHILA CNS DEVELOPMENTR01NS028182 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI Engin Ozkan, KAI G ZINN · 1990 to 2026
$7.3M
Molecular Genetics of CNS DevelopmentR37NS028182 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ZINN, KAI G · 2014 to 2020
$3.3M
Signaling Mechanisms in Drosophila Neural DevelopmentR01NS043416 · NINDS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI ZINN, KAI G · 2004 to 2007
$1.2M
NINDS NIH HHS R01 NS028182NINDS NIH HHS R01 NS043416NINDS NIH HHS R01 NS28182NINDS NIH HHS R37 NS028182
6 · The paper itself

Abstract

backgroundRoundabout (Robo) receptors and their ligand Slit are important regulators of axon guidance and cell migration. The development of Drosophila embryonic sense organs provides a neuronal migration paradigm where the in vivo roles of Slit and Robo can be assayed using genetics.

resultsHere we show that Slit-Robo signaling controls migration of Drosophila larval sensory neurons that are part of the Chordotonal (Cho) stretch receptor organs. We used live imaging to show that abdominal Cho organs normally migrate ventrally during development, whereas thoracic Cho organs do not. Robo2 overexpression in cis (in the sensory neurons) or in trans (on neighboring visceral mesoderm) transforms abdominal organs to a thoracic morphology and position by blocking migration, while loss of Slit-Robo signaling produces a reverse transformation in which thoracic organs migrate ectopically. Rescue and tissue-specific knockout experiments indicate that trans signaling by Robo2 contributes to the normal positioning of the thoracic Cho organs. The differential positioning of Cho organs between the thorax and abdomen is known to be regulated by Hox genes, and we show that the essential Hox cofactor Homothorax, represses Robo2 expression in the abdominal visceral mesoderm.

conclusionsOur results suggest that segment-specific neuronal migration patterns are directed through a novel signaling complex (the "Slit sandwich") in which Robo2 on the thoracic visceral mesoderm binds to Slit and presents it to Robo receptors on Cho neurons. The differential positioning of Cho organs between thorax and abdomen may be determined by Hox gene-mediated repression of robo2.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsAxonsBody PatterningCell MovementDrosophilaDrosophila ProteinsGreen Fluorescent ProteinsLuminescent ProteinsMechanoreceptorsModels, BiologicalNerve Tissue ProteinsReceptors, ImmunologicRoundabout ProteinsSignal TransductionDrosophila ProteinsGreen Fluorescent ProteinsLuminescent ProteinsNerve Tissue ProteinsReceptors, ImmunologicRobo2 protein, DrosophilaRoundabout Proteinssli protein, Drosophila

Identifiers

PMID15296748
PMCPMC3566263
OpenAlexW1973881489

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.