A family study implicates GBE1 in the etiology of autism spectrum disorder
Journal Title
Human Mutation
Publication Type
epub ahead of print
Abstract
Autism spectrum disorders (ASD) are neurodevelopmental disorders with an estimated heritability of >60%. Family-based genetic studies of ASD have generally focused on multiple small kindreds, searching for de novo variants of major effect. We hypothesised that molecular genetic analysis of large multiplex families would enable the identification of variants of milder effect. We studied a large multigenerational family of European ancestry with multiple family members affected with ASD or the broader autism phenotype (BAP). We identified a rare heterozygous variant in the gene encoding 1,4-alpha-glucan branching enzyme 1 (GBE1) that was present in seven of seven individuals with ASD, nine of ten individuals with the BAP and none of four tested unaffected individuals. We genotyped a community-acquired cohort of 389 individuals with ASD and identified three additional probands. Cascade analysis demonstrated the variant was present in eleven of thirteen individuals with familial ASD/BAP and neither of the two tested unaffected individuals in these three families, also of European ancestry. The variant was not enriched in the combined UK10K ASD cohorts of European ancestry but heterozygous GBE1 deletion was overrepresented in large ASD cohorts, collectively suggesting an association between GBE1 and ASD. This article is protected by copyright. All rights reserved.
Keywords
Autism Spectrum Disorder; Broader Autism Phenotype; genetics; glycogen branching enzyme; linkage; whole exome sequencing
Research Division(s)
Population Health And Immunity
PubMed ID
34633740
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2021-10-26 10:03:43
Last Modified: 2021-10-26 10:25:10
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