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Abstract Title:

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.

Abstract Source:

Sci Transl Med. 2010 Sep 15 ;2(49):49ra68. PMID: 20844286

Abstract Author(s):

Abdul Noor, Annabel Whibley, Christian R Marshall, Peter J Gianakopoulos, Amelie Piton, Andrew R Carson, Marija Orlic-Milacic, Anath C Lionel, Daisuke Sato, Dalila Pinto, Irene Drmic, Carolyn Noakes, Lili Senman, Xiaoyun Zhang, Rong Mo, Julie Gauthier, Jennifer Crosbie, Alistair T Pagnamenta, Jeffrey Munson, Annette M Estes, Andreas Fiebig, Andre Franke, Stefan Schreiber, Alexandre F R Stewart, Robert Roberts, Ruth McPherson, Stephen J Guter, Edwin H Cook, Geraldine Dawson, Gerard D Schellenberg, Agatino Battaglia, Elena Maestrini, , Linda Jeng, Terry Hutchison, Evica Rajcan-Separovic, Albert E Chudley, Suzanne M E Lewis, Xudong Liu, Jeanette J Holden, Bridget Fernandez, Lonnie Zwaigenbaum, Susan E Bryson, Wendy Roberts, Peter Szatmari, Louise Gallagher, Michael R Stratton, Jozef Gecz, Angela F Brady, Charles E Schwartz, Russell J Schachar, Anthony P Monaco, Guy A Rouleau, Chi-Chung Hui, F Lucy Raymond, Stephen W Scherer, John B Vincent

Article Affiliation:

Abdul Noor

Abstract:

Autism is a common neurodevelopmental disorder with a complex mode of inheritance. It is one of the most highly heritable of the complex disorders, although the underlying genetic factors remain largely unknown. Here, we report mutations in the X-chromosome PTCHD1 (patched-related) gene in seven families with autism spectrum disorder (ASD) and in three families with intellectual disability. A 167-kilobase microdeletion spanning exon 1 was found in two brothers, one with ASD and the other with a learning disability and ASD features; a 90-kilobase microdeletion spanning the entire gene was found in three males with intellectual disability in a second family. In 900 probands with ASD and 208 male probands with intellectual disability, we identified seven different missense changes (in eight male probands) that were inherited from unaffected mothers and not found in controls. Two of the ASD individuals with missense changes also carried a de novo deletion at another ASD susceptibility locus (DPYD and DPP6), suggesting complex genetic contributions. In additional males with ASD, we identified deletions in the 5' flanking region of PTCHD1 that disrupted a complex noncoding RNA and potential regulatory elements; equivalent changes were not found in male control individuals. Thus, our systematic screen of PTCHD1 and its 5' flanking regions suggests that this locus is involved in ~1% of individuals with ASD and intellectual disability.

Study Type : Human Study

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