Cargando…

Slit-independent guidance of longitudinal axons by Drosophila Robo3

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Carranza, Abigail, Howard, LaFreda J., Brown, Haley E., Ametepe, Ayawovi Selom, Evans, Timothy A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197545/
https://www.ncbi.nlm.nih.gov/pubmed/37214810
http://dx.doi.org/10.1101/2023.05.08.539901
_version_ 1785044573550018560
author Carranza, Abigail
Howard, LaFreda J.
Brown, Haley E.
Ametepe, Ayawovi Selom
Evans, Timothy A.
author_facet Carranza, Abigail
Howard, LaFreda J.
Brown, Haley E.
Ametepe, Ayawovi Selom
Evans, Timothy A.
author_sort Carranza, Abigail
collection PubMed
description 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.
format Online
Article
Text
id pubmed-10197545
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-101975452023-05-20 Slit-independent guidance of longitudinal axons by Drosophila Robo3 Carranza, Abigail Howard, LaFreda J. Brown, Haley E. Ametepe, Ayawovi Selom Evans, Timothy A. bioRxiv Article 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. Cold Spring Harbor Laboratory 2023-05-09 /pmc/articles/PMC10197545/ /pubmed/37214810 http://dx.doi.org/10.1101/2023.05.08.539901 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Carranza, Abigail
Howard, LaFreda J.
Brown, Haley E.
Ametepe, Ayawovi Selom
Evans, Timothy A.
Slit-independent guidance of longitudinal axons by Drosophila Robo3
title Slit-independent guidance of longitudinal axons by Drosophila Robo3
title_full Slit-independent guidance of longitudinal axons by Drosophila Robo3
title_fullStr Slit-independent guidance of longitudinal axons by Drosophila Robo3
title_full_unstemmed Slit-independent guidance of longitudinal axons by Drosophila Robo3
title_short Slit-independent guidance of longitudinal axons by Drosophila Robo3
title_sort slit-independent guidance of longitudinal axons by drosophila robo3
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197545/
https://www.ncbi.nlm.nih.gov/pubmed/37214810
http://dx.doi.org/10.1101/2023.05.08.539901
work_keys_str_mv AT carranzaabigail slitindependentguidanceoflongitudinalaxonsbydrosophilarobo3
AT howardlafredaj slitindependentguidanceoflongitudinalaxonsbydrosophilarobo3
AT brownhaleye slitindependentguidanceoflongitudinalaxonsbydrosophilarobo3
AT ametepeayawoviselom slitindependentguidanceoflongitudinalaxonsbydrosophilarobo3
AT evanstimothya slitindependentguidanceoflongitudinalaxonsbydrosophilarobo3