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使用 Illumina EPIC 阵列描述全血中常染色体 DNA 甲基化的性别差异。

Characterising sex differences of autosomal DNA methylation in whole blood using the Illumina EPIC array.

机构信息

School of Life Sciences, University of Essex, Colchester, CO4 3SQ, UK.

Institute of Social and Economic Research, University of Essex, Colchester, CO4 3SQ, UK.

出版信息

Clin Epigenetics. 2022 May 14;14(1):62. doi: 10.1186/s13148-022-01279-7.

Abstract

BACKGROUND

Sex differences are known to play a role in disease aetiology, progression and outcome. Previous studies have revealed autosomal epigenetic differences between males and females in some tissues, including differences in DNA methylation patterns. Here, we report for the first time an analysis of autosomal sex differences in DNAme using the Illumina EPIC array in human whole blood by performing a discovery (n = 1171) and validation (n = 2471) analysis.

RESULTS

We identified and validated 396 sex-associated differentially methylated CpG sites (saDMPs) with the majority found to be female-biased CpGs (74%). These saDMP's are enriched in CpG islands and CpG shores and located preferentially at 5'UTRs, 3'UTRs and enhancers. Additionally, we identified 266 significant sex-associated differentially methylated regions overlapping genes, which have previously been shown to exhibit epigenetic sex differences, and novel genes. Transcription factor binding site enrichment revealed enrichment of transcription factors related to critical developmental processes and sex determination such as SRY and ESR1.

CONCLUSION

Our study reports a reliable catalogue of sex-associated CpG sites and elucidates several characteristics of these sites using large-scale discovery and validation data sets. This resource will benefit future studies aiming to investigate sex specific epigenetic signatures and further our understanding of the role of DNA methylation in sex differences in human whole blood.

摘要

背景

性别差异已知在疾病的病因学、进展和结果中起作用。先前的研究已经在一些组织中揭示了男性和女性之间常染色体的表观遗传差异,包括 DNA 甲基化模式的差异。在这里,我们首次通过在人类全血中使用 Illumina EPIC 阵列进行发现(n=1171)和验证(n=2471)分析,报告了常染色体性别差异在 DNAme 中的分析。

结果

我们鉴定并验证了 396 个与性别相关的差异甲基化 CpG 位点(saDMPs),其中大多数是雌性偏倚的 CpG(74%)。这些 saDMPs 在 CpG 岛和 CpG 岸上富集,优先位于 5'UTR、3'UTR 和增强子。此外,我们鉴定了 266 个与基因重叠的具有显著性别差异的差异甲基化区域,这些基因先前已经显示出表观遗传性别差异和新基因。转录因子结合位点富集显示与关键发育过程和性别决定相关的转录因子如 SRY 和 ESR1 的富集。

结论

我们的研究报告了一个可靠的与性别相关的 CpG 位点目录,并使用大规模的发现和验证数据集阐明了这些位点的几个特征。该资源将有利于未来旨在研究特定性别表观遗传特征并进一步了解 DNA 甲基化在人类全血性别差异中的作用的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8394/9107695/3d9c8d1d3d82/13148_2022_1279_Fig1_HTML.jpg

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