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基于阵列的 DNA 甲基化分析揭示了男性不育症外周血中的差异甲基化。

Array-based DNA methylation profiling reveals peripheral blood differential methylation in male infertility.

机构信息

Division of Endocrinology, Central Drug Research Institute, Lucknow, India.

Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi, India.

出版信息

Fertil Steril. 2019 Jul;112(1):61-72.e1. doi: 10.1016/j.fertnstert.2019.03.020. Epub 2019 May 15.

Abstract

OBJECTIVE

To study peripheral blood DNA differential methylation in oligozoospermic infertile men in comparison with normozoospermic fertile controls.

DESIGN

Case-control study.

SETTING

Reproductive biology laboratory.

PATIENTS(S): Azoospermic and oligozoospermic infertile patients (n = 6) and normozoospermic fertile controls (n = 6) in the discovery phase, and oligo/asthenozoospermic infertile men (n = 11) and normozoospermic fertile controls (n = 10) in the validation phase.

INTERVENTION(S): Blood samples drawn from all participants, DNA isolation and methylation analysis.

MAIN OUTCOME MEASURE(S): DNA methylation values analyzed using genomewide methylation 450K BeadChip array, followed by deep sequencing of selected regions for methylation analysis in the neighborhood regions of differentially methylated CpGs.

RESULT(S): We found 329 differentially methylated CpG spots, out of which 245 referred to the genes, representing 170 genes. Deep-sequencing analysis confirmed the methylation pattern suggested by 450K array. A thorough literature search suggested that 38 genes play roles in spermatogenesis (PDHA2, PARP12, FHIT, RPTOR, GSTM1, GSTM5, MAGI2, BCAN, DDB2, KDM4C, AGPAT3, CAMTA1, CCR6, CUX1, DNAH17, ELMO1, FNDC3B, GNRHR, HDAC4, IRS2, LIF, SMAD3, SOD3, TALDO1, TRIM27, GAA, PAX8, RNF39, HLA-C, HLA-DRB6), are testis enriched (NFATC1, NMNAT3, PIAS2, SRPK2, WDR36, WWP2), or show methylation differences between infertile cases and controls (PTPRN2, RPH3AL).

CONCLUSION(S): We found a statistically significant correlation between peripheral blood DNA methylation and male infertility, raising the hope that epigenome-based blood markers can be used for screening male infertility risk. The study also identified new candidates for spermatogenesis and fertility.

摘要

目的

研究少精子症不育男性与正常生育力对照组外周血 DNA 差异甲基化。

设计

病例对照研究。

地点

生殖生物学实验室。

患者

在发现阶段,无精子症和少精子症不育患者(n=6)和正常生育力对照组(n=6),在验证阶段,少精子症和弱精子症不育男性(n=11)和正常生育力对照组(n=10)。

干预

从所有参与者中抽取血样,提取 DNA 并进行甲基化分析。

主要观察指标

采用全基因组甲基化 450K BeadChip 芯片分析 DNA 甲基化值,然后对差异甲基化 CpG 附近区域进行甲基化分析的选定区域进行深度测序。

结果

我们发现了 329 个差异甲基化 CpG 点,其中 245 个与基因有关,代表 170 个基因。深度测序分析证实了 450K 阵列所提示的甲基化模式。深入的文献检索表明,38 个基因在精子发生中起作用(PDHA2、PARP12、FHIT、RPTOR、GSTM1、GSTM5、MAGI2、BCAN、DDB2、KDM4C、AGPAT3、CAMTA1、CCR6、CUX1、DNAH17、ELMO1、FNDC3B、GNRHR、HDAC4、IRS2、LIF、SMAD3、SOD3、TALDO1、TRIM27、GAA、PAX8、RNF39、HLA-C、HLA-DRB6),是睾丸富集(NFATC1、NMNAT3、PIAS2、SRPK2、WDR36、WWP2),或在不育病例和对照组之间显示出甲基化差异(PTPRN2、RPH3AL)。

结论

我们发现外周血 DNA 甲基化与男性不育之间存在统计学显著相关性,这增加了基于表观基因组的血液标志物可用于男性不育风险筛查的希望。该研究还确定了新的精子发生和生育候选基因。

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