Publication: Ciliogenesis defects after neurulation impact brain development and neuronal activity in larval zebrafish
dc.contributor.coauthor | D'Gama, Percival P. | |
dc.contributor.coauthor | Jeong, Inyoung | |
dc.contributor.coauthor | Nygard, Andreas Moe | |
dc.contributor.coauthor | Trinh, Anh-Tuan | |
dc.contributor.coauthor | Jurisch-Yaksi, Nathalie | |
dc.contributor.department | KUTTAM (Koç University Research Center for Translational Medicine) | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Yakşi, Emre | |
dc.contributor.schoolcollegeinstitute | Research Center | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2024-12-29T09:38:12Z | |
dc.date.issued | 2024 | |
dc.description.abstract | Cilia are slender, hair -like structures extending from cell surfaces and playing essential roles in diverse physiological processes. Within the nervous system, primary cilia contribute to signaling and sensory perception, while motile cilia facilitate cerebrospinal fluid flow. Here, we investigated the impact of ciliary loss on neural circuit development using a zebrafish line displaying ciliogenesis defects. We found that cilia defects after neurulation affect neurogenesis and brain morphology, especially in the cerebellum, and lead to altered gene expression profiles. Using whole brain calcium imaging, we measured reduced light -evoked and spontaneous neuronal activity in all brain regions. By shedding light on the intricate role of cilia in neural circuit formation and function in the zebrafish, our work highlights their evolutionary conserved role in the brain and sets the stage for future analysis of ciliopathy models. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 6 | |
dc.description.openaccess | gold | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.sponsorship | We thank Zhaoxia Sun for sharing the Arl13b antibody, our fish facility team for husbandry maintenance and technical support, Konika Chawla from BioCore facility NTNU for providing help with normalizing the RNA-seq data, and all members of the Jurisch-Yaksi and Yaksi laboratories for their feedback on this work and exchanging MATLAB codes. This work was supported by funding from an NTNU strategy grant (NJY) , The Research Council of Norway: RCN FRIPRO grant 314189 (N.J.Y.) and 314212 (EY) , Horizon MSCA-2021-PF Grant 101066743 (A.-T.T.) and the Deutsche Forschungsgemeinschaft (DFG, Germany Research Foundation) , FOR5547-Project -ID 503306912 (N.J.Y.) . Work in the EY lab is funded by the Kavli Institute for Systems Neuroscience at NTNU. | |
dc.description.volume | 27 | |
dc.identifier.doi | 10.1016/j.isci.2024.110078 | |
dc.identifier.eissn | 2589-0042 | |
dc.identifier.quartile | Q1 | |
dc.identifier.scopus | 2-s2.0-85194502807 | |
dc.identifier.uri | https://doi.org/10.1016/j.isci.2024.110078 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/22588 | |
dc.identifier.wos | 1249051400001 | |
dc.keywords | Biological sciences | |
dc.keywords | Developmental neuroscience | |
dc.keywords | Neuroscience | |
dc.language.iso | eng | |
dc.publisher | Cell Press | |
dc.relation.ispartof | iScience | |
dc.subject | Medicine | |
dc.title | Ciliogenesis defects after neurulation impact brain development and neuronal activity in larval zebrafish | |
dc.type | Journal Article | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Yakşi, Emre | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit1 | Research Center | |
local.publication.orgunit2 | KUTTAM (Koç University Research Center for Translational Medicine) | |
local.publication.orgunit2 | School of Medicine | |
relation.isOrgUnitOfPublication | 91bbe15d-017f-446b-b102-ce755523d939 | |
relation.isOrgUnitOfPublication | d02929e1-2a70-44f0-ae17-7819f587bedd | |
relation.isOrgUnitOfPublication.latestForDiscovery | 91bbe15d-017f-446b-b102-ce755523d939 | |
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