Journal article
Evidence supporting WNT2 as an autism susceptibility gene
American journal of medical genetics, Vol.105(5), pp.406-413
07/08/2001
DOI: 10.1002/ajmg.1401
PMID: 11449391
Abstract
We examined WNT2 as a candidate disease gene for autism for the following reasons. First, the WNT family of genes influences the development of numerous organs and systems, including the central nervous system. Second, WNT2 is located in the region of chromosome 7q31–33 linked to autism and is adjacent to a chromosomal breakpoint in an individual with autism. Third, a mouse knockout of Dvl1, a member of a gene family essential for the function of the WNT pathway, exhibits a behavioral phenotype characterized primarily by diminished social interaction. We screened the WNT2 coding sequence for mutations in a large number of autistic probands and found two families containing nonconservative coding sequence variants that segregated with autism in those families. We also identified linkage disequilibrium (LD) between a WNT2 3′UTR SNP and our sample of autism‐affected sibling pair (ASP) families and trios. The LD arose almost exclusively from a subgroup of our ASP families defined by the presence of severe language abnormalities and was also found to be associated with the evidence for linkage to 7q from our previously published genomewide linkage screen. Furthermore, expression analysis demonstrated WNT2 expression in the human thalamus. Based on these findings, we hypothesize that rare mutations occur in the WNT2 gene that significantly increase susceptibility to autism even when present in single copies, while a more common WNT2 allele (or alleles) not yet identified may exist that contributes to the disorder to a lesser degree. © 2001 Wiley‐Liss, Inc.
Details
- Title: Subtitle
- Evidence supporting WNT2 as an autism susceptibility gene
- Creators
- Thomas H WassinkJoseph PivenVeronica J VielandJian HuangRuth E SwiderskiJennifer PietilaTerry BraunGretel BeckSusan E FolsteinJonathon L HainesVal C Sheffield
- Resource Type
- Journal article
- Publication Details
- American journal of medical genetics, Vol.105(5), pp.406-413
- DOI
- 10.1002/ajmg.1401
- PMID
- 11449391
- NLM abbreviation
- Am J Med Genet
- ISSN
- 0148-7299
- eISSN
- 1096-8628
- Publisher
- John Wiley & Sons, Inc; New York
- Number of pages
- 8
- Language
- English
- Date published
- 07/08/2001
- Academic Unit
- Statistics and Actuarial Science; Roy J. Carver Department of Biomedical Engineering; Electrical and Computer Engineering; Psychiatry; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Medical Genetics and Genomics; Ophthalmology and Visual Sciences
- Record Identifier
- 9984003489502771
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