Evidence map›Paper›PMID 39909366›Full record

ArticleDevelopmental biology2025

Slit-independent guidance of longitudinal axons by Drosophila Robo3.

Abigail Carranza, LaFreda J Howard, Haley E Brown, Ayawovi Selom Ametepe, Timothy A Evans

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Article in Developmental biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Abigail CarranzaDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR, 72701, USA.
LaFreda J HowardDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR, 72701, USA.
Haley E BrownDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR, 72701, USA.
Ayawovi Selom AmetepeDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR, 72701, USA.
Timothy A EvansDepartment of Biological Sciences, University of Arkansas, Fayetteville, AR, 72701, USA. Electronic address: evanst@uark.edu.

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Functional analysis of the Drosophila axon guidance receptor Robo2R15NS098406 · NINDS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI EVANS, TIMOTHY A. · 2016 to 2023
$1.3M
NIH HHS P40 OD018537NINDS NIH HHS R15 NS098406
6 · The paper itself

Abstract

Drosophila Robo3 is a member of the evolutionarily conserved Roundabout (Robo) receptor family and one of three Drosophila Robo paralogs. During embryonic ventral nerve cord development, Robo3 does not participate in canonical Slit-dependent midline repulsion, but instead regulates the formation of longitudinal axon pathways at specific positions along the medial-lateral axis. Longitudinal axon guidance by Robo3 is hypothesized to be Slit dependent, but this has not been directly tested. Here we create a series of Robo3 variants in which the N-terminal Ig1 domain is deleted or modified, in order to characterize the functional importance of Ig1 and Slit binding for Robo3's axon guidance activity. We show that Robo3 requires its Ig1 domain for interaction with Slit and for proper axonal localization in embryonic neurons, but deleting Ig1 from Robo3 only partially disrupts longitudinal pathway formation. Robo3 variants with modified Ig1 domains that cannot bind Slit retain proper localization and fully rescue longitudinal axon guidance. Our results indicate that Robo3 guides longitudinal axons independently of Slit, and that sequences both within and outside of Ig1 contribute to this Slit-independent activity.

Indexed as

Axon GuidanceAxonsDrosophila melanogasterDrosophila ProteinsNerve Tissue ProteinsReceptors, ImmunologicAnimalsRoundabout ProteinsDrosophila ProteinsNerve Tissue ProteinsReceptors, Immunologicrobo3 protein, DrosophilaRoundabout Proteinssli protein, Drosophila

Identifiers

PMID39909366
PMCPMC11908893

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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.