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精子异质性导致附睾头中观察到的精子DNA甲基化变异,与DNA甲基转移酶/双加氧酶活性无关。

Sperm Heterogeneity Accounts for Sperm DNA Methylation Variations Observed in the Caput Epididymis, Independently From DNMT/TET Activities.

作者信息

Chen Hong, Scott-Boyer Marie-Pier, Droit Arnaud, Robert Claude, Belleannée Clémence

机构信息

Faculty of Medicine, Université Laval, Quebec, QC, Canada.

Center for Research in Reproduction, Development and Intergenerational Health, Quebec, QC, Canada.

出版信息

Front Cell Dev Biol. 2022 Mar 22;10:834519. doi: 10.3389/fcell.2022.834519. eCollection 2022.

Abstract

Following their production in the testis, spermatozoa enter the epididymis where they gain their motility and fertilizing abilities. This post-testicular maturation coincides with sperm epigenetic profile changes that influence progeny outcome. While recent studies highlighted the dynamics of small non-coding RNAs in maturing spermatozoa, little is known regarding sperm methylation changes and their impact at the post-fertilization level. Fluorescence-activated cell sorting (FACS) was used to purify spermatozoa from the testis and different epididymal segments (i.e., ) of CAG/su9-DsRed2; Acr3-EGFP transgenic mice in order to map out sperm methylome dynamics. Reduced representation bisulfite sequencing (RRBS-Seq) performed on DNA from these respective sperm populations indicated that high methylation changes were observed between spermatozoa from the vs. testis with 5,546 entries meeting our threshold values (q value <0.01, methylation difference above 25%). Most of these changes were transitory during epididymal sperm maturation according to the low number of entries identified between spermatozoa from vs. testis. According to enzymatic and sperm/epididymal fluid co-incubation assays, (de)methylases were not found responsible for these sperm methylation changes. Instead, we identified that a subpopulation of spermatozoa displayed distinct methylation marks that were susceptible to sperm DNAse treatment and accounted for the DNA methylation profile changes observed in the proximal epididymis. Our results support the paradigm that a fraction of spermatozoa has a higher propensity to bind extracellular DNA, a phenomenon responsible for the sperm methylome variations observed at the post-testicular level. Further investigating the degree of conservation of this sperm heterogeneity in human will eventually provide new considerations regarding sperm selection procedures used in fertility clinics.

摘要

精子在睾丸中产生后,进入附睾,在那里获得运动能力和受精能力。这种睾丸后成熟过程与精子表观遗传谱变化同时发生,而这些变化会影响后代结局。虽然最近的研究强调了成熟精子中小非编码RNA的动态变化,但关于精子甲基化变化及其在受精后水平的影响却知之甚少。为了绘制精子甲基化组动态图谱,利用荧光激活细胞分选(FACS)从CAG/su9-DsRed2; Acr3-EGFP转基因小鼠的睾丸和不同附睾节段(即)中纯化精子。对这些各自精子群体的DNA进行的简化代表性亚硫酸氢盐测序(RRBS-Seq)表明,在附睾精子与睾丸精子之间观察到高度甲基化变化,有5546个条目符合我们的阈值(q值<0.01,甲基化差异超过25%)。根据附睾精子与睾丸精子之间鉴定出的条目数量较少,这些变化中的大多数在附睾精子成熟过程中是短暂的。根据酶促和精子/附睾液共孵育试验,未发现(去)甲基化酶是这些精子甲基化变化的原因。相反,我们发现一部分附睾精子显示出独特且易受精子DNA酶处理影响的甲基化标记,这解释了在附睾近端观察到的DNA甲基化谱变化。我们的结果支持这样一种模式,即一部分附睾精子具有更高的结合细胞外DNA的倾向,这一现象导致了在睾丸后水平观察到的精子甲基化组变化。进一步研究人类中这种精子异质性的保守程度最终将为生育诊所使用的精子选择程序提供新的思考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cea9/8981467/06f4b55e2969/fcell-10-834519-g001.jpg

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