Further gene mutations linked to autism risk

Pieces in the complex autism inheritance puzzle are emerging in the latest study from a research team including geneticists from the University of Pennsylvania School of Medicine and The Children's Hospital of Philadelphia (CHOP). The study identified 27 different genetic regions where rare copy number variations – missing or extra copies of DNA segments – were found in the genes of children with autism spectrum disorders, but not in the healthy controls. The findings are published June 26 in the open-access journal PLoS Genetics.

Autism spectrum disorders (ASDs) are common neurodevelopmental syndromes with a strong genetic component. ASDs are characterized by disturbances in social behavior, impaired verbal and nonverbal communication, repetitive behaviors and/or a restricted range of interests. The genetics underlying ASDs is complex and remains poorly understood.

The researchers compared genetic samples of 3,832 individuals from 912 families with multiple autistic children against genetic samples of 1,070 disease-free children. Besides the identification of 27 regions harboring rare variants in children with ASDs, the study also uncovered two novel genes where variations were found, BZRAP1 and MDGA2 – thought to be important in synaptic function and neurological development, respectively. Interestingly, key variants on these genes were passed down in some, but not all, of the affected individuals in families.

"We focused on changes in the exons of DNA—protein-coding areas in which deletions or duplications are more likely to directly disrupt biological functions," said study leader Hakon Hakonarson. "We identified additional autism susceptibility genes, many of which belong to the neuronal cell adhesion molecule family involved in the development of brain circuitry in early childhood." He added that the team discovered many "private" gene mutations, those found only in one or a few individuals or families—an indication of genetic complexity, in which many different gene changes may contribute to an autism spectrum disorder.

Hakonarson and co-author Maja Bucan said the latest findings reinforce the view that multiple gene variants, both common and rare, may be interacting to cause the heterogeneous group of disorders included under autism spectrum disorders. "We are finding that both inherited and new, or de novo, genetic mutations are scattered throughout the genome, and it is becoming clear that different combinations of these variations contribute to autism susceptibility," said Bucan.

The Autism Genetic Resource Exchange (AGRE), a program of Autism Speaks, provided genetic biomaterials and clinical data from families that have more than one family member diagnosed with an Autism Spectrum Disorder. Blood samples donated by children and their families at CHOP were used as healthy controls. AGRE makes data publicly available to qualified researchers worldwide.

FINANCIAL DISCLOSURE: The Autism Genetic Resource Exchange is a program of Autism Speaks and is supported, in part, by grant 1U24MH081810 from the National Institute of Mental Health to Clara M. Lajonchere. This work is supported by a seed grant from Penn/CHOP Center for Autism Research, by NIH grant R01MH604687, and a NARSAD Distinguished Investigator Award; by Pennsylvania Commonwealth HRFF and P20-GM69012; by the Intramural Research Program of the National Institute on Aging, National Institutes of Health, Department of Health and Human Services (1 Z01 AG000949-02); by a fellowship from the Tourette Syndrome Association; by an Autism Center of Excellence Award (P50HD055784-01); by an Autism Center of Excellence Genetics Network grant (MH081754); by a Research Award from the Margaret Q. Landenberger Foundation; by a Research Development Award from the Cotswold Foundation; and by UL1-RR024134-03. The genotyping and other aspects of the study were funded by an Institutional Development Award to the Center for Applied Genomics from the Children's Hospital of Philadelphia. 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: Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, et al. (2009) Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes. PLoS Genet 5(6): e1000536. doi:10.1371/journal.pgen.1000536

PLEASE ADD THE LINK TO THE PUBLISHED ARTICLE IN ONLINE VERSIONS OF YOUR REPORT: http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1000536

CONTACT:

Kim Guenther
University of Pennsylvania School of Medicine
(215) 200-2312
Kim.Guenther@uphs.upenn.edu

John Ascenzi
The Children's Hospital of Philadelphia
267-426-6055
Ascenzi@email.chop.edu

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