期刊
JOURNAL OF MEDICAL GENETICS
卷 48, 期 1, 页码 48-54出版社
BMJ PUBLISHING GROUP
DOI: 10.1136/jmg.2010.079426
关键词
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资金
- Simons Foundation
- Nancy Lurie Marks Family Foundation
- Wellcome Trust [075491/Z/04]
- NIH [MH086117]
- Telethon Grant [GGP06208A/B]
- Autism Speaks, Autistica
- Genome Canada/Ontario Genomics Institute
- Canadian Institutes for Health Research
- Centre for Applied Genomics and the McLaughlin Centre
- NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH086117] Funding Source: NIH RePORTER
- MRC [G0601030, G0700089, G9900837] Funding Source: UKRI
- Medical Research Council [G0700089, G9900837, G0601030] Funding Source: researchfish
Background Autism spectrum disorder (ASD) is characterised by impairments in social communication and by a pattern of repetitive behaviours, with learning disability (LD) typically seen in up to 70% of cases. A recent study using the PPL statistical framework identified a novel region of genetic linkage on chromosome 16q21 that is limited to ASD families with LD. Methods In this study, two families with autism and/or LD are described which harbour rare > 1.6 Mb microdeletions located within this linkage region. The deletion breakpoints are mapped at base-pair resolution and segregation analysis is performed using a combination of 1M single nucleotide polymorphism (SNP) technology, array comparative genomic hybridisation (CGH), long-range PCR, and Sanger sequencing. The frequency of similar genomic variants in control subjects is determined through analysis of published SNP array data. Expression of CDH8, the only gene disrupted by these microdeletions, is assessed using reverse transcriptase PCR and in situ hybridisation analysis of 9 week human embryos. Results The deletion of chr16: 60 025 584-61 667 839 was transmitted to three of three boys with autism and LD and none of four unaffected siblings, from their unaffected mother. In a second family, an overlapping deletion of chr16: 58 724 527-60 547 472 was transmitted to an individual with severe LD from his father with moderate LD. No copy number variations (CNVs) disrupting CDH8 were observed in 5023 controls. Expression analysis indicates that the two CDH8 isoforms are present in the developing human cortex. Conclusion Rare familial 16q21 microdeletions and expression analysis implicate CDH8 in susceptibility to autism and LD.
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