Title: Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.
Authors: Nord, Alex S; Roeb, Wendy; Dickel, Diane E; Walsh, Tom; Kusenda, Mary; O'Connor, Kristen Lewis; Malhotra, Dheeraj; McCarthy, Shane E; Stray, Sunday M; Taylor, Susan M; Sebat, Jonathan; STAART Psychopharmacology Network; King, Bryan; King, Mary-Claire; McClellan, Jon M
Published In Eur J Hum Genet, (2011 Jun)
Abstract: Individuals with autism are more likely to carry rare inherited and de novo copy number variants (CNVs). However, further research is needed to establish which CNVs are causal and the mechanisms by which these CNVs influence autism. We examined genomic DNA of children with autism (N = 41) and healthy controls (N = 367) for rare CNVs using a high-resolution array comparative genomic hybridization platform. We show that individuals with autism are more likely to harbor rare CNVs as small as ∼ 10 kb, a threshold not previously detectable, and that CNVs in cases disproportionately affect genes involved in transcription, nervous system development, and receptor activity. We also show that a subset of genes that have known or suspected allele-specific or imprinting effects and are within rare-case CNVs may undergo loss of transcript expression. In particular, expression of CNTNAP2 and ZNF214 are decreased in probands compared with their unaffected transmitting parents. Furthermore, expression of PRODH and ARID1B, two genes affected by de novo CNVs, are decreased in probands compared with controls. These results suggest that for some genes affected by CNVs in autism, reduced transcript expression may be a mechanism of pathogenesis during neurodevelopment.
PubMed ID: 21448237
MeSH Terms: Autistic Disorder/genetics*; Case-Control Studies; Child; Comparative Genomic Hybridization; DNA-Binding Proteins/genetics; DNA-Binding Proteins/metabolism; Gene Dosage*; Gene Expression Regulation, Developmental*; Genome, Human; Humans; Membrane Proteins/genetics; Membrane Proteins/metabolism; Nerve Tissue Proteins/genetics; Nerve Tissue Proteins/metabolism; Proline Oxidase/genetics; Proline Oxidase/metabolism; RNA, Messenger/analysis*; RNA, Messenger/biosynthesis; Transcription Factors/genetics; Transcription Factors/metabolism; Transcription, Genetic