Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/138934
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dc.contributor.authorTantra, M.en_US
dc.contributor.authorGuo, L.en_US
dc.contributor.authorKim, J.en_US
dc.contributor.authorNorliyana Zainolabidinen_US
dc.contributor.authorEulenburg, V.en_US
dc.contributor.authorAugustine, George J.en_US
dc.contributor.authorChen, Albert I-Mingen_US
dc.date.accessioned2020-05-14T04:07:35Z-
dc.date.available2020-05-14T04:07:35Z-
dc.date.issued2018-
dc.identifier.citationTantra, M., Guo, L., Kim, J., Norliyana Zainolabidin., Eulenburg, V., Augustine, G. J., & Chen, A. I.-M. (2018). Conditional deletion of Cadherin 13 perturbs Golgi cells and disrupts social and cognitive behaviors. Genes, brain, and behavior, 17(6), e12466-. doi:10.1111/gbb.12466en_US
dc.identifier.issn1601-1848en_US
dc.identifier.urihttps://hdl.handle.net/10356/138934-
dc.description.abstractInhibitory interneurons mediate the gating of synaptic transmission and modulate the activities of neural circuits. Disruption of the function of inhibitory networks in the forebrain is linked to impairment of social and cognitive behaviors, but the involvement of inhibitory interneurons in the cerebellum has not been assessed. We found that Cadherin 13 (Cdh13), a gene implicated in autism spectrum disorder and attention-deficit hyperactivity disorder, is specifically expressed in Golgi cells within the cerebellar cortex. To assess the function of Cdh13 and utilize the manipulation of Cdh13 expression in Golgi cells as an entry point to examine cerebellar-mediated function, we generated mice carrying Cdh13-floxed alleles and conditionally deleted Cdh13 with GlyT2::Cre mice. Loss of Cdh13 results in a decrease in the expression/localization of GAD67 and reduces spontaneous inhibitory postsynaptic current (IPSC) in cerebellar Golgi cells without disrupting spontaneous excitatory postsynaptic current (EPSC). At the behavioral level, loss of Cdh13 in the cerebellum, piriform cortex and endopiriform claustrum have no impact on gross motor coordination or general locomotor behaviors, but leads to deficits in cognitive and social abilities. Mice lacking Cdh13 exhibit reduced cognitive flexibility and loss of preference for contact region concomitant with increased reciprocal social interactions. Together, our findings show that Cdh13 is critical for inhibitory function of Golgi cells, and that GlyT2::Cre-mediated deletion of Cdh13 in non-executive centers of the brain, such as the cerebellum, may contribute to cognitive and social behavioral deficits linked to neurological disorders.en_US
dc.description.sponsorshipMOE (Min. of Education, S’pore)en_US
dc.description.sponsorshipNMRC (Natl Medical Research Council, S’pore)en_US
dc.language.isoenen_US
dc.relation.ispartofGenes, brain, and behavioren_US
dc.rights© 2018 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.en_US
dc.subjectScience::Biological sciencesen_US
dc.titleConditional deletion of Cadherin 13 perturbs Golgi cells and disrupts social and cognitive behaviorsen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.contributor.schoolLee Kong Chian School of Medicine (LKCMedicine)en_US
dc.identifier.doi10.1111/gbb.12466-
dc.description.versionPublished versionen_US
dc.identifier.pmid29446202-
dc.identifier.scopus2-s2.0-85043699590-
dc.identifier.issue6en_US
dc.identifier.volume17en_US
dc.subject.keywordsAutism Spectrum Disorderen_US
dc.subject.keywordsCadherin 13en_US
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