Public Release: 

Further support for a role of synaptic proteins in autism spectrum disorders

A new study combines genetic and neurobiological approaches to confirm that synaptic mutations increase the risk of autism spectrum disorders (ASDs)

PLOS

A new study combines genetic and neurobiological approaches to confirm that synaptic mutations increase the risk of autism spectrum disorders (ASDs). It also highlights a role for modifier genes in these disorders. Published in PLoS Genetics, this research was conducted by researchers at the Institut Pasteur, the Paris Diderot University, the Robert Debré Hospital, the Gillberg Neuropsychiatry centre, Ulm University and the Centre National de Génotypage, in collaboration with other institutions in Europe.

ASDs are a heterogeneous group of neurodevelopmental disorders with a complex inheritance pattern characterized by impairments in social interaction and communication, and by restricted and repetitive behavior. ASDs appear before the age of three years and affect 1/100 children, with a higher risk for males than for females. Several genes involved in ASD have been identified in patients with ASD, but only recently have we started to learn about their effects on neuronal functions and their interaction with other genetic variations.

In their new study, Leblond and collaborators identified mutations altering SHANK2, a gene that encodes a scaffolding protein located at synapses (contacts between neuronal cells). The researchers showed that several of the mutations observed in patients reduced the number of synapses in neuronal cell cultures. Further genomic analysis of three patients carrying SHANK2 deletions identified additional rare genomic imbalances, previously associated with other neuropsychiatric disorders, that could act as modifier genes by modulating the disorder.

These results emphasise the importance of synaptic gene dysfunction in ASD and also highlight a role for modifier genes, confirming a "multiple hit model" for ASD. "A better knowledge of these genetic interactions will be necessary to understand the complex inheritance pattern of ASD", concludes Thomas Bourgeron, an author on the paper.

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FINANCIAL DISCLOSURE: This work was supported by the Institut Pasteur, INSERM, APHP, ANR (ANR-08-MNPS-037-01 - SynGen), Neuron-ERANET (EUHF-AUTISM), Fondation Orange, Fondation pour la Recherche Me´ dicale, RTRS Sante´ Mentale (Foundation FondaMental), the Deutsche Forschungsgemeinschaft DFG (BO1718:3-1 and SFB497/B8), the Dutch Foundation for Brain Research (Hersenstichting, grant # 2008(1).34), and Wellcome Trust core grant (075491/Z/04). D Pinto is supported by a postdoctoral fellowship from the Canadian Institutes of Health Research (#213997). SW Scherer holds the GlaxoSmithKline-CIHR Pathfinder Chair in Genetics and Genomics at the University of Toronto and the Hospital for Sick Children. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

COMPETING INTERESTS: The authors have declared that no competing interests exist.

CITATION: Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, et al. (2012) Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders. PLoS Genet 8(2): e1002521. doi:10.1371/journal.pgen.1002521

PLEASE ADD THIS LINK TO THE FREELY AVAILABLE ARTICLE IN ONLINE VERSIONS OF YOUR REPORT (the link will go live when the embargo ends): http://www.plosgenetics.org/doi/pgen.1002521

PRESS-ONLY PREVIEW OF THE ARTICLE: http://www.plos.org/media/press/2012/plge-08-02-Leblond.pdf

CONTACT:
Thomas Bourgeron
Institut Pasteur
Neuroscience
25 rue du Docteur Roux
Paris, 75015
FRANCE
Phone: (33) 1 40 61 32 16
Email: thomasb@pasteur.fr

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