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人类精子中的组蛋白修饰特征可区分临床异常。

Histone modification signatures in human sperm distinguish clinical abnormalities.

机构信息

Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of Pennsylvania, 3701 Market Street, Suite 800, Philadelphia, PA, 19104, USA.

Division of Reproductive Endocrinology & Infertility, Department of Obstetrics and Gynecology, University of Michigan Medical School, L4000 UH-South, 1500 E. Medical Center Drive, Ann Arbor, MI, 48109, USA.

出版信息

J Assist Reprod Genet. 2019 Feb;36(2):267-275. doi: 10.1007/s10815-018-1354-7. Epub 2018 Nov 5.

Abstract

PURPOSE

Alternations to the paternal epigenome, specifically the components of sperm chromatin, can lead to infertility in humans and potentially transmit aberrant information to the embryo. One key component of sperm chromatin is the post-translational modification of histones (PTMs). We previously identified a comprehensive profile of histone PTMs in normozoospermic sperm; however, only specific histone PTMs have been identified in abnormal sperm by antibody-based approaches and comprehensive changes to histone PTM profiles remain unknown. Here, we investigate if sperm with abnormalities of total motility, progressive motility, and morphology have altered histone PTM profiles compared to normozoospermic sperm samples.

METHODS

Discarded semen samples from 31 men with normal or abnormal semen parameters were analyzed for relative abundance of PTMs on histone H3 and H4 by "bottom-up" nano-liquid chromatography-tandem mass spectrometry.

RESULTS

Asthenoteratozoospermic samples (abnormal motility, forward progression, and morphology, n = 6) displayed overall decreased H4 acetylation (p = 0.001) as well as alterations in H4K20 (p = 0.003) and H3K9 methylation (p < 0.04) when compared to normozoospermic samples (n = 8). Asthenozoospermic samples (abnormal motility and progression, n = 5) also demonstrated decreased H4 acetylation (p = 0.04) and altered H4K20 (p = 0.005) and H3K9 methylation (p < 0.04). Samples with isolated abnormal progression (n = 6) primarily demonstrated decreased acetylation on H4 (p < 0.02), and teratozoospermic samples (n = 6) appeared similar to normozoospermic samples (n = 8).

CONCLUSION

Sperm samples with combined and isolated abnormalities of total motility, progressive motility, and morphology display distinct and altered histone PTM signatures compared to normozoospermic sperm. This provides evidence that alterations in histone PTMs may be important for normal sperm function and fertility.

摘要

目的

父系表观基因组的改变,特别是精子染色质的成分,可导致人类不育,并可能向胚胎传递异常信息。精子染色质的一个关键组成部分是组蛋白的翻译后修饰(PTMs)。我们之前在正常精子中鉴定了组蛋白 PTM 的综合特征;然而,通过基于抗体的方法仅鉴定了异常精子中的特定组蛋白 PTM,并且组蛋白 PTM 谱的综合变化仍然未知。在这里,我们研究了总活力、前向运动和形态异常的精子与正常精子样本相比是否具有改变的组蛋白 PTM 谱。

方法

对 31 名精液参数正常或异常的男性的废弃精液样本进行分析,通过“自上而下”的纳升液相色谱-串联质谱法检测组蛋白 H3 和 H4 上 PTM 的相对丰度。

结果

弱精畸形精子样本(异常活力、前向运动和形态,n=6)与正常精子样本(n=8)相比,整体显示出 H4 乙酰化降低(p=0.001),以及 H4K20(p=0.003)和 H3K9 甲基化改变(p<0.04)。弱精样本(异常活力和前向运动,n=5)也表现出 H4 乙酰化降低(p=0.04)和 H4K20(p=0.005)和 H3K9 甲基化改变(p<0.04)。孤立异常前向运动的样本(n=6)主要表现为 H4 乙酰化降低(p<0.02),而畸形精子样本(n=6)与正常精子样本(n=8)相似。

结论

总活力、前向运动和形态联合和孤立异常的精子样本显示出与正常精子不同的改变的组蛋白 PTM 特征。这表明组蛋白 PTM 的改变可能对正常精子功能和生育能力很重要。

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