| Literature DB >> 26068849 |
Jonas Richiardi1, Andre Altmann2, Anna-Clare Milazzo3, Catie Chang4, M Mallar Chakravarty5, Tobias Banaschewski6, Gareth J Barker7, Arun L W Bokde8, Uli Bromberg9, Christian Büchel9, Patricia Conrod10, Mira Fauth-Bühler11, Herta Flor12, Vincent Frouin13, Jürgen Gallinat14, Hugh Garavan15, Penny Gowland16, Andreas Heinz14, Hervé Lemaître17, Karl F Mann11, Jean-Luc Martinot17, Frauke Nees12, Tomáš Paus18, Zdenka Pausova19, Marcella Rietschel20, Trevor W Robbins21, Michael N Smolka22, Rainer Spanagel23, Andreas Ströhle14, Gunter Schumann24, Mike Hawrylycz25, Jean-Baptiste Poline26, Michael D Greicius27.
Abstract
During rest, brain activity is synchronized between different regions widely distributed throughout the brain, forming functional networks. However, the molecular mechanisms supporting functional connectivity remain undefined. We show that functional brain networks defined with resting-state functional magnetic resonance imaging can be recapitulated by using measures of correlated gene expression in a post mortem brain tissue data set. The set of 136 genes we identify is significantly enriched for ion channels. Polymorphisms in this set of genes significantly affect resting-state functional connectivity in a large sample of healthy adolescents. Expression levels of these genes are also significantly associated with axonal connectivity in the mouse. The results provide convergent, multimodal evidence that resting-state functional networks correlate with the orchestrated activity of dozens of genes linked to ion channel activity and synaptic function.Entities:
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Year: 2015 PMID: 26068849 PMCID: PMC4829082 DOI: 10.1126/science.1255905
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728