Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19975
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dc.contributor.authorO'Neill, Adam C-
dc.contributor.authorKyrousi, Christina-
dc.contributor.authorKlaus, Johannes-
dc.contributor.authorLeventer, Richard J-
dc.contributor.authorKirk, Edwin P-
dc.contributor.authorFry, Andrew-
dc.contributor.authorPilz, Daniela T-
dc.contributor.authorMorgan, Tim-
dc.contributor.authorJenkins, Zandra A-
dc.contributor.authorDrukker, Micha-
dc.contributor.authorBerkovic, Samuel F-
dc.contributor.authorScheffer, Ingrid E-
dc.contributor.authorGuerrini, Renzo-
dc.contributor.authorMarkie, David M-
dc.contributor.authorGötz, Magdalena-
dc.contributor.authorCappello, Silvia-
dc.contributor.authorRobertson, Stephen P-
dc.date.accessioned2019-01-02T01:13:21Z-
dc.date.available2019-01-02T01:13:21Z-
dc.date.issued2018-12-04-
dc.identifier.citationCell reports 2018; 25(10): 2729-2741.e6-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19975-
dc.description.abstractThe mammalian neocortex has undergone remarkable changes through evolution. A consequence of such rapid evolutionary events could be a trade-off that has rendered the brain susceptible to certain neurodevelopmental and neuropsychiatric conditions. We analyzed the exomes of 65 patients with the structural brain malformation periventricular nodular heterotopia (PH). De novo coding variants were observed in excess in genes defining a transcriptomic signature of basal radial glia, a cell type linked to brain evolution. In addition, we located two variants in human isoforms of two genes that have no ortholog in mice. Modulating the levels of one of these isoforms for the gene PLEKHG6 demonstrated its role in regulating neuroprogenitor differentiation and neuronal migration via RhoA, with phenotypic recapitulation of PH in human cerebral organoids. This suggests that this PLEKHG6 isoform is an example of a primate-specific genomic element supporting brain development.-
dc.language.isoeng-
dc.subjectMyoGEF-
dc.subjectPLEKHG6-
dc.subjectRhoA-
dc.subjectcortical development-
dc.subjectevolution-
dc.subjectperiventricular heterotopia-
dc.titleA Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration.-
dc.typeJournal Article-
dc.identifier.journaltitleCell reports-
dc.identifier.affiliationInstitute of Medical Genetics, University Hospital of Wales, Heath Park, Cardiff CF14 4XW, UKen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, VIC 3052, Australiaen
dc.identifier.affiliationInstitute of Stem Cell Research, Helmholtz Center, Munich, Germanyen
dc.identifier.affiliationMax Planck Institute of Psychiatry, Munich, Germanyen
dc.identifier.affiliationInstitute of Stem Cell Research, Helmholtz Center, Munich, Germanyen
dc.identifier.affiliationPhysiological Genomics, Biomedical Center Ludwig-Maximilians-Universitaet, Munich, Germanyen
dc.identifier.affiliationExcellence Cluster of Systems Neurology (SYNERGY), 82152 Planegg/Martinsried, Germanyen
dc.identifier.affiliationWest of Scotland Genetics Service, Laboratory Medicine Building, Queen Elizabeth University Hospital, Glasgow G51 4TF, UKen
dc.identifier.affiliationEpilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Neurology, Murdoch Children's Research Institute, Parkville, Victoria, Australiaen
dc.identifier.affiliationDepartment of Paediatrics, University of Melbourne, Parkville, Victoria, Australiaen
dc.identifier.affiliationSydney Children's Hospital, University of New South Wales, Randwick, NSW, Australiaen
dc.identifier.affiliationNew South Wales Health Pathology, Randwick, NSW, Australiaen
dc.identifier.affiliationDepartment of Women's and Children's Health, University of Otago, Dunedin, New Zealand-
dc.identifier.affiliationPediatric Neurology Unit and Laboratories, Children's Hospital A. Meyer-University of Florence, Florence, Italy-
dc.identifier.affiliationDepartment of Pathology, University of Otago, Dunedin, New Zealand-
dc.identifier.affiliationMax Planck Institute of Psychiatry, Munich, Germany-
dc.identifier.doi10.1016/j.celrep.2018.11.029-
dc.identifier.orcid0000-0002-2311-2174-
dc.identifier.orcid0000-0003-4580-841X-
dc.identifier.pubmedid30517861-
dc.type.austinJournal Article-
local.name.researcherBerkovic, Samuel F
item.languageiso639-1en-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
crisitem.author.deptEpilepsy Research Centre-
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