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Series GSE108785 Query DataSets for GSE108785
Status Public on Dec 31, 2018
Title Methylomic Analysis reveals Epigenetic Pattern of SH2B1 in Chinese Monozygotic Twins Discordant for Autism Spectrum Disorder [Methylation 450K]
Organism Homo sapiens
Experiment type Methylation profiling by genome tiling array
Summary Autism spectrum disorder(ASD) is a complex neurodevelopmental disorder. Aberrant DNA methylation has been observed in ASD but the mechanisms remain largely unknown. Here, we employed discordant monozygotic twins to investigate the contribution of DNA methylation to ASD etiology. Genome-wide DNA methylation analysis was performed using samples obtained from five pairs of ASD-discordant monozygotic twins, which revealed a total of 2397 differentially methylated genes. Further, such gene list was annotated with Kyoto Encyclopedia of Genes and Genomes and demonstrated predominant activation of neurotrophin signaling pathway in ASD-discordant monozygotic twins. The methylation of SH2B1 gene was further confirmed in the ASD-discordant, ASD-concordant monozygotic twins, and a set of 30 pairs of sporadic case-control by bisulfite-pyrosequencing. The results showed that there was a greater DNA methylation difference in ASD-discordant monozygotic twins than ASD-concordant monozygotic twins. Further, verification of the Chr.16:28856743 of SH2B1 showed significant differences in DNA methylation between case and control. These results suggest abnormal methylation of SH2B1 is associated with ASD etiology. Our data suggest that it might be worthwhile to further explore the functions of SH2B1 and related genes of neurotrophin signaling pathway in ASD.
 
Overall design Whole blood samples were obtained from five monozygotic twin paris with discordant ASD. Samples from two twin pairs underwent Reduced representation bisulfite sequencing (RRBS) and three twin pairs underwent Infinium 450K to determine methylation level.
 
Contributor(s) Liang S, Li Z, Wang Y, Li H, Yang X, Wang X, Zhan X, Huang Y, Li X, Gao Z, Zhang M, Wang J, Fan L, Xia W, Zhang Y, Wu L
Citation(s) 31379474
Submission date Jan 04, 2018
Last update date Mar 23, 2020
Contact name Zhenzhi Li
E-mail(s) [email protected]
Organization name Georgetown University
Department Biochemistry and Molecular Biology
Street address 3900 reservoir rd nw
City Washington
State/province DC
ZIP/Postal code 20007
Country USA
 
Platforms (1)
GPL13534 Illumina HumanMethylation450 BeadChip (HumanMethylation450_15017482)
Samples (6)
GSM2913200 TP1_case
GSM2913201 TP2_case
GSM2913202 TP3_case
This SubSeries is part of SuperSeries:
GSE108815 Methylomic Analysis reveals Epigenetic Pattern of SH2B1 in Chinese Monozygotic Twins Discordant for Autism Spectrum Disorder
Relations
BioProject PRJNA428733

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE108785_RAW.tar 231.9 Mb (http)(custom) TAR (of IDAT)
GSE108785_signal_intensity.txt.gz 7.7 Mb (ftp)(http) TXT
Processed data included within Sample table

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