Hypomethylation of Wnt signaling regulator genes in developmental language disorder.

IF 3 4区 医学 Q2 GENETICS & HEREDITY
Epigenomics Pub Date : 2024-02-01 Epub Date: 2024-01-24 DOI:10.2217/epi-2023-0345
Mary Iype, Nisha Melempatt, Jesmy James, Sanjeev V Thomas, Ayyappan Anitha
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引用次数: 0

Abstract

Background: Developmental language disorder (DLD) is a neurodevelopmental disorder. Considering the pivotal role of epigenetics in neurodevelopment, we examined any altered DNA methylation between DLD and control subjects. Materials & methods: We looked into genome-wide methylation differences between DLD and control groups. The findings were validated by quantitative PCR (qPCR). Results: In the DLD group, differential methylation of CpG sites was observed in the Wnt signaling regulator genes APCDD1, AMOTL1, LRP5, MARK2, TMEM64, TRABD2B, VEPH1 and WNT2B. Hypomethylation of APCDD1, LRP5 and WNT2B was confirmed by qPCR. Conclusion: This is the first report associating Wnt signaling with DLD. The findings are relevant in the light of the essential role of Wnt in myelination, and of the altered myelination in DLD.

发育性语言障碍中 Wnt 信号调节基因的低甲基化。
背景介绍发育性语言障碍(DLD)是一种神经发育障碍。考虑到表观遗传学在神经发育过程中的关键作用,我们研究了发育性语言障碍患者与对照组之间 DNA 甲基化的变化。材料与方法:我们研究了 DLD 和对照组之间的全基因组甲基化差异。研究结果通过定量 PCR(qPCR)进行了验证。结果在 DLD 组中,Wnt 信号调节基因 APCDD1、AMOTL1、LRP5、MARK2、TMEM64、TRABD2B、VEPH1 和 WNT2B 的 CpG 位点甲基化存在差异。qPCR证实了APCDD1、LRP5和WNT2B的低甲基化。结论这是第一份将 Wnt 信号与 DLD 联系起来的报告。鉴于 Wnt 在髓鞘形成中的重要作用以及 DLD 中髓鞘形成的改变,该研究结果具有重要意义。
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来源期刊
Epigenomics
Epigenomics GENETICS & HEREDITY-
CiteScore
5.80
自引率
2.60%
发文量
95
审稿时长
>12 weeks
期刊介绍: Epigenomics provides the forum to address the rapidly progressing research developments in this ever-expanding field; to report on the major challenges ahead and critical advances that are propelling the science forward. The journal delivers this information in concise, at-a-glance article formats – invaluable to a time constrained community. Substantial developments in our current knowledge and understanding of genomics and epigenetics are constantly being made, yet this field is still in its infancy. Epigenomics provides a critical overview of the latest and most significant advances as they unfold and explores their potential application in the clinical setting.
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