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|Title:||Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease|
|Authors:||Johnson, Michael R;Shkura, Kirill;Langley, Sarah R;Delahaye-Duriez, Andree;Srivastava, Prashant M;Hill, W David;Rackham, Owen JL;Davies, Gail;Harris, Sarah E;Moreno-Moral, Aida;Rotival, Maxime;Petrovski, Slavé;Katz, Anaïs;Hayward, Caroline;Porteous, David J;Smith, Blair H;Padmanabhan, Sandosh;Hocking, Lynne J;Starr, John M;Liewald, David C;Visconti, Alessia;Falchi, Mario;Bottolo, Leonardo;Rossetti, Tiziana;Danis, Bénédicte;Mazzuferi, Manuela;Foerch, Patrik;Grote, Alexander;Helmstaedter, Christoph;Becker, Albert J;Kaminski, Rafal M;Deary, Ian J;Petretto, Enrico;Speed, Doug|
|Citation:||Nature Neuroscience 2016; 19(2): 223-32|
|Abstract:||Genetic determinants of cognition are poorly characterized, and their relationship to genes that confer risk for neurodevelopmental disease is unclear. Here we performed a systems-level analysis of genome-wide gene expression data to infer gene-regulatory networks conserved across species and brain regions. Two of these networks, M1 and M3, showed replicable enrichment for common genetic variants underlying healthy human cognitive abilities, including memory. Using exome sequence data from 6,871 trios, we found that M3 genes were also enriched for mutations ascertained from patients with neurodevelopmental disease generally, and intellectual disability and epileptic encephalopathy in particular. M3 consists of 150 genes whose expression is tightly developmentally regulated, but which are collectively poorly annotated for known functional pathways. These results illustrate how systems-level analyses can reveal previously unappreciated relationships between neurodevelopmental disease-associated genes in the developed human brain, and provide empirical support for a convergent gene-regulatory network influencing cognition and neurodevelopmental disease.|
Gene regulatory networks
|Appears in Collections:||Journal articles|
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