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研究导致瘦体和肥胖体脂肪生成差异的基因表达改变相关的 DNA 甲基化变化。

Investigation of changes in DNA methylation associated with alterations in gene expression resulting in differences between lean and obese adipogenesis.

机构信息

Division of Biomedical Convergence, College of Biomedical Science, Institute of Bioscience & Biotechnology, Kangwon National University, Chuncheon 24341, Republic of Korea.

Division of Biomedical Convergence, College of Biomedical Science, Institute of Bioscience & Biotechnology, Kangwon National University, Chuncheon 24341, Republic of Korea.

出版信息

Genomics. 2023 May;115(3):110623. doi: 10.1016/j.ygeno.2023.110623. Epub 2023 Apr 14.

Abstract

DNA methylation (DNAm) is an important epigenetic regulator controlling various cellular activities, including cell proliferation and differentiation. In the present work, we examined alterations in DNAm associated with obesity using methylome and transcriptome data from 27 purified adipocytes (ACs) and 7 preadipocytes (preACs) in human visceral adipose tissue (VAT) samples. We identified differentially methylated probes (DMPs) using two methods: (i) DMPs that were obtained from a comparison of the DNAm levels between AC and preAC samples (AGDMPs) and (ii) DMPs that were obtained from a comparison of the DNAm levels between obese and lean AC samples (ACDMPs). These two classes of DMPs were obtained to identify a relationship between adipogenesis and obesity. We also investigated how hyper and hypomethylation of the promoter and/or gene body differentially affected changes in gene expression by estimating the odds ratios (ORs) of changes in gene expression without DMPs in the background. Interestingly, the magnitude of DNAm alterations during AC differentiation was greater under lean conditions than under obese conditions. In conclusion, several adipogenesis-related genes were affected by complicated methylation changes and ultimately cause differences in gene expression in ACs under lean and obese conditions.

摘要

DNA 甲基化(DNAm)是一种重要的表观遗传调控因子,控制着包括细胞增殖和分化在内的各种细胞活动。在本工作中,我们使用人类内脏脂肪组织(VAT)样本中 27 个纯化脂肪细胞(AC)和 7 个前脂肪细胞(preAC)的甲基组和转录组数据,研究了与肥胖相关的 DNAm 改变。我们使用两种方法识别差异甲基化探针(DMPs):(i)通过比较 AC 和 preAC 样本之间的 DNAm 水平获得的 DMPs(AGDMPs)和(ii)通过比较肥胖和瘦 AC 样本之间的 DNAm 水平获得的 DMPs(ACDMPs)。这两类 DMPs 的获得是为了识别脂肪生成和肥胖之间的关系。我们还通过估计没有 DMP 背景下基因表达变化的比值比(ORs),研究了启动子和/或基因体的高甲基化和低甲基化如何差异地影响基因表达的变化。有趣的是,在瘦条件下,AC 分化过程中的 DNAm 改变幅度大于肥胖条件下。总之,几种与脂肪生成相关的基因受到复杂的甲基化变化的影响,最终导致在瘦和肥胖条件下 AC 中的基因表达存在差异。

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