Publication:
Ciliogenesis defects after neurulation impact brain development and neuronal activity in larval zebrafish

dc.contributor.coauthorD'Gama, Percival P.
dc.contributor.coauthorJeong, Inyoung
dc.contributor.coauthorNygard, Andreas Moe
dc.contributor.coauthorTrinh, Anh-Tuan
dc.contributor.coauthorJurisch-Yaksi, Nathalie
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorYakşi, Emre
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-12-29T09:38:12Z
dc.date.issued2024
dc.description.abstractCilia 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.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue6
dc.description.openaccessgold
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipWe 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.volume27
dc.identifier.doi10.1016/j.isci.2024.110078
dc.identifier.eissn2589-0042
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85194502807
dc.identifier.urihttps://doi.org/10.1016/j.isci.2024.110078
dc.identifier.urihttps://hdl.handle.net/20.500.14288/22588
dc.identifier.wos1249051400001
dc.keywordsBiological sciences
dc.keywordsDevelopmental neuroscience
dc.keywordsNeuroscience
dc.language.isoeng
dc.publisherCell Press
dc.relation.ispartofiScience
dc.subjectMedicine
dc.titleCiliogenesis defects after neurulation impact brain development and neuronal activity in larval zebrafish
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorYakşi, Emre
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit1Research Center
local.publication.orgunit2KUTTAM (Koç University Research Center for Translational Medicine)
local.publication.orgunit2School of Medicine
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