| Literature DB >> 27911742 |
Maria Chahrour1, Brian J O'Roak2, Emanuela Santini3, Rodney C Samaco4, Robin J Kleiman5, M Chiara Manzini6.
Abstract
Autism spectrum disorder (ASD) is a constellation of neurodevelopmental presentations with high heritability and both phenotypic and genetic heterogeneity. To date, mutations in hundreds of genes have been associated to varying degrees with increased ASD risk. A better understanding of the functions of these genes and whether they fit together in functional groups or impact similar neuronal circuits is needed to develop rational treatment strategies. We will review current areas of emphasis in ASD research, starting from human genetics and exploring how mouse models of human mutations have helped identify specific molecular pathways (protein synthesis and degradation, chromatin remodeling, intracellular signaling), which are linked to alterations in circuit function and cognitive/social behavior. We will conclude by discussing how we can leverage the findings on molecular and cellular alterations found in ASD to develop therapies for neurodevelopmental disorders.Entities:
Keywords: animal models; autism spectrum disorder; genetics; therapeutics
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Year: 2016 PMID: 27911742 PMCID: PMC5125207 DOI: 10.1523/JNEUROSCI.2335-16.2016
Source DB: PubMed Journal: J Neurosci ISSN: 0270-6474 Impact factor: 6.167