利用灵敏的计算方法分析全基因组亚硫酸氢盐测序数据,对系统性硬化症有了新的认识。

IF 5.7 2区 医学 Q1 Medicine Clinical Epigenetics Pub Date : 2023-06-03 DOI:10.1186/s13148-023-01513-w
Jeffrey C Y Yu, Yixiao Zeng, Kaiqiong Zhao, Tianyuan Lu, Kathleen Oros Klein, Inés Colmegna, Maximilien Lora, Sahir R Bhatnagar, Andrew Leask, Celia M T Greenwood, Marie Hudson
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引用次数: 0

摘要

背景:DNA甲基化异常被认为是系统性硬化症发病和进展的原因之一。目前,最全面的DNA甲基化分析方法是全基因组亚硫酸氢盐测序(WGBS),但其精确度取决于读取深度,而且可能会出现测序错误。SOMNiBUS 是一种区域分析方法,它试图克服其中的一些局限性。使用 SOMNiBUS,我们重新分析了之前使用 bumphunter(一种初步拟合单个 CpG 关联的方法)分析的 WGBS 数据,以对比两种方法的 DNA 甲基化估计值:使用 WGBS 对 9 名 SSc 女性和 4 名对照女性的纯化 CD4+ T 淋巴细胞进行测序。我们将测序得到的数据分成具有密集 CpG 数据的区域,并通过 SOMNiBUS 区域级测试推断出差异甲基化区域(DMR),再根据年龄进行调整。通路富集分析是通过巧妙通路分析(IPA)进行的。我们比较了 SOMNiBUS 和 bumphunter 的结果:在8268个符合SOMNiBUS分析条件的≥60个CpGs的CpG区域中,我们发现了131个DMRs和125个差异甲基化基因(DMGs;P值小于Bonferroni校正阈值6.05-06,族内误差率控制在0.05;占区域的1.6%)。相比之下,bumphunter 发现了 821 929 个 CpG 区域、599 个 DMR(其中没有一个区域的 CpG ≥ 60)和 340 个 DMG(q 值为 0.05;占所有区域的 0.04%)。SOMNiBUS确定的排名第一的基因是FLT4,它是淋巴管生成的协调者;X染色体上排名第一的基因是CHST7,它催化细胞外基质中糖胺聚糖的硫酸化。IPA确定的顶级网络包括结缔组织疾病:SOMNiBUS是分析WGBS数据的一种补充方法,它提高了对SSc的生物学认识,并为研究其发病机制提供了新的途径。
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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Novel insights into systemic sclerosis using a sensitive computational method to analyze whole-genome bisulfite sequencing data.

Background: Abnormal DNA methylation is thought to contribute to the onset and progression of systemic sclerosis. Currently, the most comprehensive assay for profiling DNA methylation is whole-genome bisulfite sequencing (WGBS), but its precision depends on read depth and it may be subject to sequencing errors. SOMNiBUS, a method for regional analysis, attempts to overcome some of these limitations. Using SOMNiBUS, we re-analyzed WGBS data previously analyzed using bumphunter, an approach that initially fits single CpG associations, to contrast DNA methylation estimates by both methods.

Methods: Purified CD4+ T lymphocytes of 9 SSc and 4 control females were sequenced using WGBS. We separated the resulting sequencing data into regions with dense CpG data, and differentially methylated regions (DMRs) were inferred with the SOMNiBUS region-level test, adjusted for age. Pathway enrichment analysis was performed with ingenuity pathway analysis (IPA). We compared the results obtained by SOMNiBUS and bumphunter.

Results: Of 8268 CpG regions of ≥ 60 CpGs eligible for analysis with SOMNiBUS, we identified 131 DMRs and 125 differentially methylated genes (DMGs; p-values less than Bonferroni-corrected threshold of 6.05-06 controlling family-wise error rate at 0.05; 1.6% of the regions). In comparison, bumphunter identified 821,929 CpG regions, 599 DMRs (of which none had ≥ 60 CpGs) and 340 DMGs (q-value of 0.05; 0.04% of all regions). The top ranked gene identified by SOMNiBUS was FLT4, a lymphangiogenic orchestrator, and the top ranked gene on chromosome X was CHST7, known to catalyze the sulfation of glycosaminoglycans in the extracellular matrix. The top networks identified by IPA included connective tissue disorders.

Conclusions: SOMNiBUS is a complementary method of analyzing WGBS data that enhances biological insights into SSc and provides novel avenues of investigation into its pathogenesis.

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来源期刊
Clinical Epigenetics
Clinical Epigenetics Biochemistry, Genetics and Molecular Biology-Developmental Biology
CiteScore
8.90
自引率
5.30%
发文量
150
审稿时长
12 weeks
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
期刊最新文献
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