Rapid publication: Evidence supporting WNT2 as an autism susceptibility gene

Thomas H. Wassink, Joseph Piven, Veronica J. Vieland, Jian Huang, Ruth E. Swiderski, Jennifer Pietila, Terry Braun, Gretel Beck, Susan E. Folstein, Jonathon L. Haines, Val C. Sheffield

Research output: Contribution to journalArticle

161 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)406-413
Number of pages8
JournalAmerican Journal of Medical Genetics - Neuropsychiatric Genetics
Volume105
Issue number5
DOIs
StatePublished - Jul 8 2001

Fingerprint

Autistic Disorder
Publications
Genes
Linkage Disequilibrium
Siblings
Alleles
Mutation
Essential Genes
Interpersonal Relations
Thalamus
Knockout Mice
Single Nucleotide Polymorphism
Language
Central Nervous System
Chromosomes
Phenotype

Keywords

  • Autism
  • Candidate gene
  • Chromosome 7q
  • Linkage disequilibrium

ASJC Scopus subject areas

  • Genetics(clinical)
  • Neuropsychology and Physiological Psychology
  • Neuroscience(all)
  • Genetics

Cite this

Wassink, T. H., Piven, J., Vieland, V. J., Huang, J., Swiderski, R. E., Pietila, J., ... Sheffield, V. C. (2001). Rapid publication: Evidence supporting WNT2 as an autism susceptibility gene. American Journal of Medical Genetics - Neuropsychiatric Genetics, 105(5), 406-413. https://doi.org/10.1002/ajmg.1401

Rapid publication : Evidence supporting WNT2 as an autism susceptibility gene. / Wassink, Thomas H.; Piven, Joseph; Vieland, Veronica J.; Huang, Jian; Swiderski, Ruth E.; Pietila, Jennifer; Braun, Terry; Beck, Gretel; Folstein, Susan E.; Haines, Jonathon L.; Sheffield, Val C.

In: American Journal of Medical Genetics - Neuropsychiatric Genetics, Vol. 105, No. 5, 08.07.2001, p. 406-413.

Research output: Contribution to journalArticle

Wassink, TH, Piven, J, Vieland, VJ, Huang, J, Swiderski, RE, Pietila, J, Braun, T, Beck, G, Folstein, SE, Haines, JL & Sheffield, VC 2001, 'Rapid publication: Evidence supporting WNT2 as an autism susceptibility gene', American Journal of Medical Genetics - Neuropsychiatric Genetics, vol. 105, no. 5, pp. 406-413. https://doi.org/10.1002/ajmg.1401
Wassink, Thomas H. ; Piven, Joseph ; Vieland, Veronica J. ; Huang, Jian ; Swiderski, Ruth E. ; Pietila, Jennifer ; Braun, Terry ; Beck, Gretel ; Folstein, Susan E. ; Haines, Jonathon L. ; Sheffield, Val C. / Rapid publication : Evidence supporting WNT2 as an autism susceptibility gene. In: American Journal of Medical Genetics - Neuropsychiatric Genetics. 2001 ; Vol. 105, No. 5. pp. 406-413.
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