Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis

Adolescent idiopathic scoliosis (AIS) is a complex disease affecting a large number of teenagers, especially in female. This study reveals novel epigenetic perturbation to the pathogenesis of AIS. A female monozygotic (MZ) twin pair discordant for AIS were examined for whole-exome sequencing and epi...

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Published inFrontiers in bioengineering and biotechnology Vol. 7; p. 364
Main Authors Liu, Gang, Wang, Lianlei, Wang, Xinyu, Yan, Zihui, Yang, Xinzhuang, Lin, Mao, Liu, Sen, Zuo, Yuzhi, Niu, Yuchen, Zhao, Sen, Zhao, Yanxue, Zhang, Jianguo, Shen, Jianxiong, Wang, Yipeng, Qiu, Guixing, Wu, Zhihong, Wu, Nan
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 10.12.2019
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Summary:Adolescent idiopathic scoliosis (AIS) is a complex disease affecting a large number of teenagers, especially in female. This study reveals novel epigenetic perturbation to the pathogenesis of AIS. A female monozygotic (MZ) twin pair discordant for AIS were examined for whole-exome sequencing and epigenome difference. Sets of differentially methylated regions (DMRs) were validated using MethylTarget™ method in 20 AIS female patients and 20 healthy female controls. Few exome difference but several potential DMRs were found between the MZ twins. We identified 313 hypermethylated DMRs and 397 hypomethylated DMRs, respectively. Most of them were enriched in the MAPK and PI3K-Akt signaling pathway, which may contribute to the discordance of AIS. Several DMRs related to scoliosis genes were tested, and the : TSS-DMR (chr15:23932133-23932304, hg19) was confirmed in additional samples. The methylation level of this DMR was significantly higher in the AIS group than in the control group ( = 0.04). We described the epigenome difference in an AIS female discordant MZ twin pair using Whole Genome Bisulfite Sequencing (WGBS). The : TSS-DMR had higher methylation level in female AIS, which can help elucidate the potential etiology of AIS.
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This article was submitted to Bioinformatics and Computational Biology, a section of the journal Frontiers in Bioengineering and Biotechnology
Edited by: Yongchun Zuo, Inner Mongolia University, China
These authors have contributed equally to this work
Reviewed by: Enrique Medina-Acosta, Universidade Estadual do Norte Fluminense Darcy Ribeiro, Brazil; Jie Zhang, Tongji University, China
ISSN:2296-4185
2296-4185
DOI:10.3389/fbioe.2019.00364