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Cachd1 interacts with Wnt receptors and regulates neuronal asymmetry in the zebrafish brain.

Powell, GT; Faro, A; Zhao, Y; Stickney, H; Novellasdemunt, L; Henriques, P; Gestri, G; Redhouse White, E; Ren, J; Lu, W; et al. Powell, GT; Faro, A; Zhao, Y; Stickney, H; Novellasdemunt, L; Henriques, P; Gestri, G; Redhouse White, E; Ren, J; Lu, W; Young, RM; Hawkins, TA; Cavodeassi, F; Schwarz, Q; Dreosti, E; Raible, DW; Li, VSW; Wright, GJ; Jones, EY; Wilson, SW (2024) Cachd1 interacts with Wnt receptors and regulates neuronal asymmetry in the zebrafish brain. Science, 384 (6695). pp. 573-579. ISSN 1095-9203 https://doi.org/10.1126/science.ade6970
SGUL Authors: Cavodeassi, Florencia

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Abstract

Neurons on the left and right sides of the nervous system often show asymmetric properties, but how such differences arise is poorly understood. Genetic screening in zebrafish revealed that loss of function of the transmembrane protein Cachd1 resulted in right-sided habenula neurons adopting left-sided identity. Cachd1 is expressed in neuronal progenitors, functions downstream of asymmetric environmental signals, and influences timing of the normally asymmetric patterns of neurogenesis. Biochemical and structural analyses demonstrated that Cachd1 can bind simultaneously to Lrp6 and Frizzled family Wnt co-receptors. Consistent with this, lrp6 mutant zebrafish lose asymmetry in the habenulae, and epistasis experiments support a role for Cachd1 in modulating Wnt pathway activity in the brain. These studies identify Cachd1 as a conserved Wnt receptor-interacting protein that regulates lateralized neuronal identity in the zebrafish brain.

Item Type: Article
Additional Information: Copyright © 2024 the authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original US government works. https://www.science.org/about/science-licenses-journal-article-reuse. This research was funded in whole or in part by the Wellcome Trust (104682/Z/14/Z, 088175/Z/09/Z, 225445/Z/22/Z, 223133/Z/21/Z, 206194, and 101122/Z/13/Z, FC001105), a cOAlition S organization. The authors will make the Author Accepted Manuscript (AAM) version available under a CC BY public copyright license.
Keywords: Animals, Zebrafish, Zebrafish Proteins, Habenula, Neurons, Neurogenesis, Wnt Signaling Pathway, Low Density Lipoprotein Receptor-Related Protein-6, Frizzled Receptors, Receptors, Wnt, Brain, Loss of Function Mutation, Membrane Proteins, Brain, Habenula, Neurons, Animals, Zebrafish, Zebrafish Proteins, Membrane Proteins, Frizzled Receptors, Neurogenesis, Low Density Lipoprotein Receptor-Related Protein-6, Wnt Signaling Pathway, Receptors, Wnt, Loss of Function Mutation, Animals, Brain, Frizzled Receptors, Habenula, Loss of Function Mutation, Low Density Lipoprotein Receptor-Related Protein-6, Membrane Proteins, Neurogenesis, Neurons, Receptors, Wnt, Wnt Signaling Pathway, Zebrafish, Zebrafish Proteins, General Science & Technology
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Biomedical Education (INMEBE)
Journal or Publication Title: Science
ISSN: 1095-9203
Language: eng
Dates:
DateEvent
3 May 2024Published
27 March 2024Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
104682/Z/14/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
088175/Z/09/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
225445/Z/22/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
MR/L003775/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/T020164/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
223133/Z/21/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
C375/A17721Cancer Research UKhttp://dx.doi.org/10.13039/501100000289
MR/M000141/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
206194Wellcome Trusthttp://dx.doi.org/10.13039/100004440
101122/Z/13/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
FC001105Cancer Research UKhttp://dx.doi.org/10.13039/501100000289
FC001105Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
FC001105Wellcome Trusthttp://dx.doi.org/10.13039/100004440
PubMed ID: 38696577
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116482
Publisher's version: https://doi.org/10.1126/science.ade6970

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