Mutation screening of the UBE3A gene in Chinese Han population with autism
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RESEARCH ARTICLE
Open Access
Mutation screening of the UBE3A gene in Chinese Han population with autism Xue Zhao, Ran Zhang and Shunying Yu*
Abstract Background: 15q11–13 region is one of the most complex chromosomal regions in the human genome. UBE3A is an important candidate gene of autism spectrum disorder (ASD), which located at the 15q11–13 region and encodes ubiquitin-protein ligase E3A. Previous studies about UBE3A gene and ASD have shown inconsistent results and few studies were performed in Chinese population. This study aimed to detect the genetic mutations of UBE3A gene in Chinese Han population with ASD and analyze genetic association between these variants and ASD. Methods: The samples consisted of 192 patients with autism according to the DSM-IV diagnostic criteria and 192 healthy controls. We searched for mutations at coding sequence (CDS) regions and their adjacent non-coding regions of UBE3A gene using the high resolution melting (HRM) and Sanger sequencing methods. We further increased sample size to validate the detected variants using HRM and conducted association analysis between case and control groups. Results: A known single nucleotide polymorphism (T > C, rs150331504) located at the CDS4 and a known 5 bp insertion/ deletion variation (AACTC+/−, rs71127053) located at the intron region of the upstream 288 bp of the CDS2 of UBE3A gene were detected using Sanger sequencing method. The ASD samples of case group were 391 for rs71127053, 384 for rs150331504 and 384 healthy controls, which were used to make an association analysis. The results of association analysis suggested that there were no significant difference about the allele and genotype frequencies of rs71127053 and rs150331504 between case and control groups after extending the sample size. Besides, rs150331504 is a synonymous mutation and we compared the secondary structure and minimum free energy (MFE) of mRNA harboring the allele T or C of rs150331504 using RNAfold software. We found that the centroid secondary structure apparently differs along with the polymorphisms of rs150331504 T > C, the results suggested that this variant might change the secondary structure of mRNA of UBE3A gene. We did not detect mutations in other coding regions of UBE3A gene. Conclusions: These findings showed that UBE3A gene might not be a major disease gene in Chinese ASD cases. Keywords: ASD, 15q11–13, UBE3A, HRM, Sequencing
Background Autism is a childhood-onset neurodevelopmental disorder characterized by impaired social interactions and communication, restricted interests and repetitive behaviors, the onset of autism is usually before 3 years old. In 2013, the fifth edition of Diagnostic and Statistical * Correspondence: [email protected] Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, 600 Wanping Nan Road, Shanghai 200030, China
Manual of Mental Disorders (DSM-5) removed delayed language development from the list of diagnose criteria, autism covered a host of diseases such as Asperger’s disorder, childhood disi
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