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Slit-independent guidance of longitudinal axons by Drosophila Robo3

Abigail Carranza, LaFreda J. Howard, Haley E. Brown, Ayawovi Selom Ametepe, View ORCID ProfileTimothy A. Evans
doi: https://doi.org/10.1101/2023.05.08.539901
Abigail Carranza
1Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701
2Texas A&M University School of Medicine, Bryan, TX 77807
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LaFreda J. Howard
1Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701
3NAVA PBC, Washington, DC 20005
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Haley E. Brown
1Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701
4Department of Biology, Indiana University, Bloomington, IN 47405, USA
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Ayawovi Selom Ametepe
1Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701
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Timothy A. Evans
1Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701
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  • ORCID record for Timothy A. Evans
  • For correspondence: evanst@uark.edu
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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.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted May 09, 2023.
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Slit-independent guidance of longitudinal axons by Drosophila Robo3
Abigail Carranza, LaFreda J. Howard, Haley E. Brown, Ayawovi Selom Ametepe, Timothy A. Evans
bioRxiv 2023.05.08.539901; doi: https://doi.org/10.1101/2023.05.08.539901
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Slit-independent guidance of longitudinal axons by Drosophila Robo3
Abigail Carranza, LaFreda J. Howard, Haley E. Brown, Ayawovi Selom Ametepe, Timothy A. Evans
bioRxiv 2023.05.08.539901; doi: https://doi.org/10.1101/2023.05.08.539901

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