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dc.contributor.authorOlsen, Lene Christin
dc.contributor.authorO'Reilly, Kally
dc.contributor.authorLiabakk, Nina-Beate
dc.contributor.authorWitter, Menno
dc.contributor.authorSætrom, Pål
dc.date.accessioned2017-12-13T12:37:15Z
dc.date.available2017-12-13T12:37:15Z
dc.date.created2017-03-21T11:51:29Z
dc.date.issued2017
dc.identifier.citationBrain Structure and Function. 2017, 222 (7), 3107-3126.nb_NO
dc.identifier.issn1863-2653
dc.identifier.urihttp://hdl.handle.net/11250/2471184
dc.description.abstractThe medial entorhinal cortex (MEC) is important in spatial navigation and memory formation and its layers have distinct neuronal subtypes, connectivity, spatial properties, and disease susceptibility. As little is known about the molecular basis for the development of these laminar differences, we analyzed microRNA (miRNA) and messenger RNA (mRNA) expression differences between rat MEC layer II and layers III–VI during postnatal development. We identified layer and age-specific regulation of gene expression by miRNAs, which included processes related to neuron specialization and locomotor behavior. Further analyses by retrograde labeling and expression profiling of layer II stellate neurons and in situ hybridization revealed that the miRNA most up-regulated in layer II, miR-143, was enriched in stellate neurons, whereas the miRNA most up-regulated in deep layers, miR-219-5p, was expressed in ependymal cells, oligodendrocytes and glia. Bioinformatics analyses of predicted mRNA targets with negatively correlated expression patterns to miR-143 found that miR-143 likely regulates the Lmo4 gene, which is known to influence hippocampal-based spatial learning.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Verlagnb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleMicroRNAs contribute to postnatal development of laminar differences and neuronal subtypes in the rat medial entorhinal cortexnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber3107–3126nb_NO
dc.source.volume222nb_NO
dc.source.journalBrain Structure and Functionnb_NO
dc.source.issue7nb_NO
dc.identifier.doi10.1007/s00429-017-1389-z
dc.identifier.cristin1459973
dc.description.localcode© The Author(s) 2017. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.nb_NO
cristin.unitcode194,65,15,0
cristin.unitcode194,65,60,0
cristin.unitcode194,63,10,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameKavliinstitutt for nevrovitenskap
cristin.unitnameInstitutt for datateknologi og informatikk
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode2


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