表观基因组-850K全谱分析揭示了足月低体重儿的外周血甲基化差异。

IF 2.6 4区 医学 Q2 GENETICS & HEREDITY Epigenomics Pub Date : 2024-01-01 Epub Date: 2024-07-03 DOI:10.1080/17501911.2024.2358744
Jing Liu, Qi Sun, Die Liu, Haixiao Liang, Yuanmei Chen, Fang Ye, Qi Zhang
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引用次数: 0

摘要

目的:我们研究了足月低出生体重(TLBW)新生儿的全基因组 DNA 甲基化(DNAm)模式。方法在发现阶段,我们使用 EPIC 850k BeadChip 阵列检测了 32 个样本(TLBW/对照:16/16)。在复制阶段,使用靶向热测序对 60 个样本(TLBW/对照组:28/32)进行靶向热测序。结果850K 阵列确定了与 TLBW 相关的 144 个差异甲基化位置(DMPs)和 149 个 DMRs。近 77% 的 DMPs 表现出低甲基化,位于 opensea 和基因体区域。KEGG 中最显着富集的途径是鞘脂代谢(hsa00600),与该途径相关的基因 GALC 和 SGMS1 均出现了低甲基化。结论我们的分析提供了 TLBW 全基因组 DNAm 改变的证据。要阐明这些 DNAm 变化的功能意义,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Epigenome-850K-wide profiling reveals peripheral blood differential methylation in term low birth weight.

Aim: We investigate the genome-wide DNA methylation (DNAm) patterns of term low birth weight (TLBW) neonates.Methods: In the discovery phase, we assayed 32 samples (TLBW/control:16/16) using the EPIC 850k BeadChip Array. Targeted pyrosequencing of in 60 samples (TLBW/control:28/32) using targeted pyrosequencing during the replication phase.Results: The 850K array identified TLBW-associated 144 differentially methylated positions (DMPs) and 149 DMRs. Nearly 77% DMPs exhibited hypomethylation, located in the opensea and gene body regions. The most significantly enriched pathway in KEGG is sphingolipid metabolism (hsa00600), and the genes GALC and SGMS1 related to this pathway both show hypomethylation.Conclusion: Our analysis provides evidence of genome-wide DNAm alterations in TLBW. Further investigations are needed to elucidate the functional significance of these DNAm changes.

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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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