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      Sex differences in brain plasticity: a new hypothesis for sex ratio bias in autism

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          Abstract

          Several observations support the hypothesis that differences in synaptic and regional cerebral plasticity between the sexes account for the high ratio of males to females in autism. First, males are more susceptible than females to perturbations in genes involved in synaptic plasticity. Second, sex-related differences in non-autistic brain structure and function are observed in highly variable regions, namely, the heteromodal associative cortices, and overlap with structural particularities and enhanced activity of perceptual associative regions in autistic individuals. Finally, functional cortical reallocations following brain lesions in non-autistic adults (for example, traumatic brain injury, multiple sclerosis) are sex-dependent. Interactions between genetic sex and hormones may therefore result in higher synaptic and consecutively regional plasticity in perceptual brain areas in males than in females. The onset of autism may largely involve mutations altering synaptic plasticity that create a plastic reaction affecting the most variable and sexually dimorphic brain regions. The sex ratio bias in autism may arise because males have a lower threshold than females for the development of this plastic reaction following a genetic or environmental event.

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          De novo gene disruptions in children on the autistic spectrum.

          Exome sequencing of 343 families, each with a single child on the autism spectrum and at least one unaffected sibling, reveal de novo small indels and point substitutions, which come mostly from the paternal line in an age-dependent manner. We do not see significantly greater numbers of de novo missense mutations in affected versus unaffected children, but gene-disrupting mutations (nonsense, splice site, and frame shifts) are twice as frequent, 59 to 28. Based on this differential and the number of recurrent and total targets of gene disruption found in our and similar studies, we estimate between 350 and 400 autism susceptibility genes. Many of the disrupted genes in these studies are associated with the fragile X protein, FMRP, reinforcing links between autism and synaptic plasticity. We find FMRP-associated genes are under greater purifying selection than the remainder of genes and suggest they are especially dosage-sensitive targets of cognitive disorders. Copyright © 2012 Elsevier Inc. All rights reserved.
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            Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

            Autism spectrum disorders (ASDs) comprise a range of disorders that share a core of neurobehavioural deficits characterized by widespread abnormalities in social interactions, deficits in communication as well as restricted interests and repetitive behaviours. The neurological basis and circuitry mechanisms underlying these abnormal behaviours are poorly understood. Shank3 is a postsynaptic protein, whose disruption at the genetic level is thought to be responsible for development of 22q13 deletion syndrome (Phelan-McDermid Syndrome) and other non-syndromic ASDs. Here we show that mice with Shank3 gene deletions exhibit self-injurious repetitive grooming and deficits in social interaction. Cellular, electrophysiological and biochemical analyses uncovered defects at striatal synapses and cortico-striatal circuits in Shank3 mutant mice. Our findings demonstrate a critical role for Shank3 in the normal development of neuronal connectivity and establish causality between a disruption in the Shank3 gene and the genesis of autistic like-behaviours in mice.
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              Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

              Many studies have supported a genetic etiology for autism. Here we report mutations in two X-linked genes encoding neuroligins NLGN3 and NLGN4 in siblings with autism-spectrum disorders. These mutations affect cell-adhesion molecules localized at the synapse and suggest that a defect of synaptogenesis may predispose to autism.
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                Author and article information

                Contributors
                laurent.mottron@gmail.com
                pauline.duret@ens-lyon.fr
                sophia.mueller@med.uni-muenchen.de
                robert.moore@umontreal.ca
                b.forgeot@gmail.com
                sebastien.jacquemont@umontreal.ca
                lan.xiong@umontreal.ca
                Journal
                Mol Autism
                Mol Autism
                Molecular Autism
                BioMed Central (London )
                2040-2392
                5 June 2015
                5 June 2015
                2015
                : 6
                : 33
                Affiliations
                [ ]Centre d’excellence en Troubles envahissants du dévelopement de l’Université de Montréal (CETEDUM), Montréal, Canada
                [ ]Hôpital Rivière-des-Prairies, Département de Psychiatrie, Montréal, Canada
                [ ]Centre de Recherche de l’Institut Universitaire en Santé Mentale de Montréal, Québec, Canada
                [ ]Department of Psychiatry, University of Montreal, Québec, Canada
                [ ]Département de Biologie, École Normale Supérieure de Lyon, Lyon, CEDEX 07 France
                [ ]Institute of Clinical Radiology, University Hospitals, Munich, Germany
                [ ]Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA 02129 USA
                [ ]Harvard University, Center for Brain Science, Cambridge, MA 02138 USA
                [ ]Department of Health Sciences, University of Montreal, Montreal, Canada
                [ ]College of Applied Health Sciences, University of Illinois, Urbana-Champaign, USA
                [ ]Centre de recherche, Centre Hospitalier Universitaire Sainte Justine, Montréal, Canada
                [ ]Service of Medical Genetics, University Hospital of Lausanne, University of Lausanne, Lausanne, 1011 Switzerland
                Article
                24
                10.1186/s13229-015-0024-1
                4456778
                26052415
                675f8a37-d93f-4493-a7df-e16b04422aba
                © Mottron et al. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 26 December 2014
                : 27 April 2015
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                Review
                Custom metadata
                © The Author(s) 2015

                Neurosciences
                autism spectrum,sex ratio,male bias,synaptic plasticity,regional plasticity,perceptual associative cortex,sexual dimorphism,enhanced perceptual functioning

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