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全基因组氧化亚硫酸氢盐测序鉴定出人胎盘性别特异性甲基化差异。

Genome-wide oxidative bisulfite sequencing identifies sex-specific methylation differences in the human placenta.

机构信息

a Department of Obstetrics and Gynaecology , University of Cambridge, NIHR Cambridge Comprehensive Biomedical Research Centre , Cambridge , CB2 0SW , United Kingdom.

b Centre for Trophoblast Research (CTR), Department of Physiology, Development and Neuroscience , University of Cambridge , Cambridge , CB2 3EG , United Kingdom.

出版信息

Epigenetics. 2018;13(3):228-239. doi: 10.1080/15592294.2018.1429857. Epub 2018 Feb 21.


DOI:10.1080/15592294.2018.1429857
PMID:29376485
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5989156/
Abstract

DNA methylation is an important regulator of gene function. Fetal sex is associated with the risk of several specific pregnancy complications related to placental function. However, the association between fetal sex and placental DNA methylation remains poorly understood. We carried out whole-genome oxidative bisulfite sequencing in the placentas of two healthy female and two healthy male pregnancies generating an average genome depth of coverage of 25x. Most highly ranked differentially methylated regions (DMRs) were located on the X chromosome but we identified a 225 kb sex-specific DMR in the body of the CUB and Sushi Multiple Domains 1 (CSMD1) gene on chromosome 8. The sex-specific differential methylation pattern observed in this region was validated in additional placentas using in-solution target capture. In a new RNA-seq data set from 64 female and 67 male placentas, CSMD1 mRNA was 1.8-fold higher in male than in female placentas (P value = 8.5 × 10, Mann-Whitney test). Exon-level quantification of CSMD1 mRNA from these 131 placentas suggested a likely placenta-specific CSMD1 isoform not detected in the 21 somatic tissues analyzed. We show that the gene body of an autosomal gene, CSMD1, is differentially methylated in a sex- and placental-specific manner, displaying sex-specific differences in placental transcript abundance.

摘要

DNA 甲基化是基因功能的重要调节因子。胎儿性别与几种与胎盘功能相关的特定妊娠并发症的风险有关。然而,胎儿性别与胎盘 DNA 甲基化之间的关联仍知之甚少。我们对两个健康女性和两个健康男性妊娠的胎盘进行了全基因组氧化亚硫酸氢盐测序,平均基因组覆盖深度为 25x。排名最高的差异甲基化区域 (DMR) 大多位于 X 染色体上,但我们在 8 号染色体的 CUB 和 Sushi 多重结构域 1 (CSMD1) 基因的主体中发现了一个 225kb 的性别特异性 DMR。使用溶液靶向捕获在额外的胎盘中验证了该区域观察到的性别特异性差异甲基化模式。在来自 64 个女性和 67 个男性胎盘的新 RNA-seq 数据集,CSMD1 mRNA 在男性胎盘中比在女性胎盘中高 1.8 倍(P 值=8.5×10,Mann-Whitney 检验)。来自这 131 个胎盘的 CSMD1 mRNA 的外显子水平定量表明,可能存在一种胎盘特异性 CSMD1 异构体,在分析的 21 种体细胞组织中未检测到。我们表明,常染色体基因 CSMD1 的基因体以性别和胎盘特异性的方式发生差异甲基化,在胎盘转录丰度上显示出性别特异性差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/b63853e0797a/kepi-13-03-1429857-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/260647e4ca1e/kepi-13-03-1429857-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/4250101f1204/kepi-13-03-1429857-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/eef660de1612/kepi-13-03-1429857-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/a835c7cd33ab/kepi-13-03-1429857-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/bf2f13516a97/kepi-13-03-1429857-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/b63853e0797a/kepi-13-03-1429857-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/260647e4ca1e/kepi-13-03-1429857-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/4250101f1204/kepi-13-03-1429857-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/eef660de1612/kepi-13-03-1429857-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/a835c7cd33ab/kepi-13-03-1429857-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/bf2f13516a97/kepi-13-03-1429857-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb5a/5997159/b63853e0797a/kepi-13-03-1429857-g006.jpg

相似文献

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[6]
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[7]
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[10]
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Evol Anthropol. 2025-6

[2]
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[3]
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[4]
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Biol Sex Differ. 2024-8-16

[5]
Sex differences in DNA methylation across gestation: a large scale, cross-cohort, multi-tissue analysis.

Cell Mol Life Sci. 2024-4-10

[6]
The application of epiphenotyping approaches to DNA methylation array studies of the human placenta.

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[7]
The application of epiphenotyping approaches to DNA methylation array studies of the human placenta.

Res Sq. 2023-6-26

[8]
Sex differences in placenta-derived markers and later autistic traits in children.

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[9]
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[10]
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本文引用的文献

[1]
Loss of CSMD1 expression disrupts mammary duct formation while enhancing proliferation, migration and invasion.

Oncol Rep. 2017-5-22

[2]
Replicated association between the European GWAS locus rs10503253 at CSMD1 and schizophrenia in Asian population.

Neurosci Lett. 2017-4-24

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Sexual epigenetic dimorphism in the human placenta: implications for susceptibility during the prenatal period.

Epigenomics. 2017-3

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Allele-Specific Methylome and Transcriptome Analysis Reveals Widespread Imprinting in the Human Placenta.

Am J Hum Genet. 2016-11-3

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Elife. 2016-8-24

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