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Canalization of neural dynamics by δ-protocadherins in the developing zebrafish optic tectum.

Overview

Authors: Sayantanee Biswas1, Michelle R. Emond1, Grace S. Philip1, James D. Jontes1
  1. Department of Biological Chemistry and Pharmacology, Ohio State University Wexner College of Medicine, Columbus, Ohio, United States of America
Institutions: The Ohio State University (United States)
Journal: PLoS genetics, volume 22, issue 6, article e1012171
Dates: received 28 August 2025; accepted 18 May 2026; published online 1 June 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1371/journal.pgen.1012171 · PMID 42224358 · PMCID PMC13241009 · OpenAlex W7163025282
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: human (organism), zebrafish (organism)
Methods: Smoothing, state filtering, decompositions, Connectivity, fMRI & imaging, Single-unit activity, calcium imaging
MeSH: Cadherins*, Superior Colliculi*, Zebrafish*, Zebrafish Proteins*, Animals, Brain, Gene Expression Regulation, Developmental, Humans, Larva, Mutation, Nerve Net, Neurodevelopment, Neurons, Protocadherins (* major topic)
Journal subjects: Biology and Life Sciences, Developmental Biology, Life Cycles, Larvae, Cell Biology, Cellular Types, Animal Cells, Neurons, Neuroscience, Cellular Neuroscience, Cognitive Science, Cognitive Psychology, Perception, Sensory Perception, Vision, Psychology, Social Sciences, Research and Analysis Methods, Animal Studies, Experimental Organism Systems, Model Organisms, Zebrafish, Animal Models, Organisms, Eukaryota, Animals, Vertebrates, Fish, Osteichthyes, Zoology, Anatomy, Brain, Superior Colliculus, Medicine and Health Sciences, Genetics, Heredity, Heterozygosity, Phenotypes, Epidemiology, Medical Risk Factors
Topic: Wnt/β-catenin signaling in development and cancer (Molecular Biology, Biochemistry, Genetics and Molecular Biology), according to OpenAlex
Citations: not cited yet (Europe PMC); 80 references in the paper
Research resources: CMV:jGCaMP8s RRID:Addgene_162371, CMV:Histone H2B-mGL RRID:Addgene_164464, Tol2-elavl3-GCaMP6s RRID:Addgene_59530

Abstract

Brain dynamics are constrained by the underlying topology of neuronal networks. How genes collaborate to organize these neural networks during development remains an enduring mystery. In humans, large numbers of genes have been implicated in neurodevelopmental disorders that are characterized by variable and overlapping phenotypes. The complexity of the brain and the heterogeneity of the disorders makes understanding the relationships between genes, development and neural function challenging. Beginning in the 1940s, Waddington suggested the concept of canalization to describe the role of genes as buffering developmental trajectories against genetic and environmental variation, leading to precise outcomes. Here, we show that members of the δ-protocadherin family of homophilic cell adhesion molecules, Protocadherin-19 and Protocadherin-17, contribute to developmental canalization of neural dynamics in the visual system of larval zebrafish. We provided oriented visual stimuli to zebrafish larvae and performed in vivo 2-photon calcium imaging in the optic tectum. The latent dynamics resulting from the population activity were remarkably conserved among different wild type larvae, allowing quantitative comparisons within and among genotypes. In both Protocadherin-19 and Protocadherin-17 mutants, the latent dynamics diverged stochastically from wild type, suggesting that the loss of these adhesion molecules leads to stochastic phenotypic variability and introduced disruptions of circuit organization that varied among individual mutants. These results are consistent with the developmental canalization of a vertebrate neural circuit, and suggest a framework for understanding the observed variability in complex brain disorders.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

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Data

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Data Availability

The data used for this manuscript are available at: https://doi.org/10.5281/zenodo.18616323.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

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Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 4 authors, 14 MeSH terms, 2 funders, 79 references, 3 RRIDs.

Cite

This paper

Biswas, S., Emond, M. R., Philip, G. S., & Jontes, J. D. (2026). Canalization of neural dynamics by δ-protocadherins in the developing zebrafish optic tectum. PLoS genetics, 22(6), e1012171. https://doi.org/10.1371/journal.pgen.1012171

BibTeX

@article{biswas2026canalization,
author = {Biswas, Sayantanee and Emond, Michelle R. and Philip, Grace S. and Jontes, James D.},
title = {{Canalization of neural dynamics by δ-protocadherins in the developing zebrafish optic tectum}},
journal = {PLoS genetics},
year = {2026},
month = jun,
volume = {22},
number = {6},
pages = {e1012171},
publisher = {PLOS},
issn = {1553-7390},
doi = {10.1371/journal.pgen.1012171},
url = {https://doi.org/10.1371/journal.pgen.1012171},
pmid = {42224358},
pmcid = {PMC13241009}
}

RIS

TY - JOUR
AU - Biswas, Sayantanee
AU - Emond, Michelle R.
AU - Philip, Grace S.
AU - Jontes, James D.
TI - Canalization of neural dynamics by δ-protocadherins in the developing zebrafish optic tectum
T2 - PLoS genetics
J2 - PLoS Genet
PY - 2026
DA - 2026/06/01
VL - 22
IS - 6
SP - e1012171
SN - 1553-7390
PB - PLOS
DO - 10.1371/journal.pgen.1012171
UR - https://doi.org/10.1371/journal.pgen.1012171
LA - en
ER -

CSL-JSON

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