Please use this identifier to cite or link to this item: https://doi.org/10.1523/ENEURO.0283-19.2019
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dc.titleDistinct genetic signatures of cortical and subcortical regions associated with human memory
dc.contributor.authorTan, P.K.
dc.contributor.authorAnanyev, E.
dc.contributor.authorHsieh, P.-J.
dc.date.accessioned2021-12-06T04:21:57Z
dc.date.available2021-12-06T04:21:57Z
dc.date.issued2019
dc.identifier.citationTan, P.K., Ananyev, E., Hsieh, P.-J. (2019). Distinct genetic signatures of cortical and subcortical regions associated with human memory. eNeuro 6 (6) : ENEURO.0283-19.2019. ScholarBank@NUS Repository. https://doi.org/10.1523/ENEURO.0283-19.2019
dc.identifier.issn2373-2822
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/209536
dc.description.abstractDespite the discovery of gene variants linked to memory performance, understanding the genetic basis of adult human memory remains a challenge. Here, we devised an unsupervised framework that relies on spatial correlations between human transcriptome data and functional neuroimaging maps to uncover the genetic signatures of memory in functionally-defined cortical and subcortical memory regions. Results were validated with animal literature and showed that our framework is highly effective in identifying memory-related processes and genes compared to a control cognitive function. Genes preferentially expressed in cortical memory regions are linked to memory-related processes such as immune and epigenetic regulation. Genes expressed in subcortical memory regions are associated with neurogenesis and glial cell differentiation. Genes expressed in both cortical and subcortical memory areas are involved in the regulation of transcription, synaptic plasticity, and glutamate receptor signaling. Furthermore, distinct memoryassociated genes such as PRKCD and CDK5 are linked to cortical and subcortical regions, respectively. Thus, cortical and subcortical memory regions exhibit distinct genetic signatures that potentially reflect functional differences in health and disease, and nominates gene candidates for future experimental investigations. © 2019 Tan et al.
dc.publisherSociety for Neuroscience
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.subjectCognition
dc.subjectCortical
dc.subjectGenetic
dc.subjectHuman
dc.subjectMemory
dc.subjectNeuroimaging
dc.typeArticle
dc.contributor.departmentLIFE SCIENCES INSTITUTE
dc.description.doi10.1523/ENEURO.0283-19.2019
dc.description.sourcetitleeNeuro
dc.description.volume6
dc.description.issue6
dc.description.pageENEURO.0283-19.2019
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