Beck Daniel, Sadler-Riggleman Ingrid, Skinner Michael K
Center for Reproductive Biology, School of Biological Sciences, Washington State University, Pullman, WA 99164-4236, USA.
Environ Epigenet. 2017 Jul;3(3). doi: 10.1093/eep/dvx016. Epub 2017 Aug 29.
Environmentally induced epigenetic transgenerational inheritance of disease and phenotypic variation has been shown to involve DNA methylation alterations in the germline (e.g. sperm). These differential DNA methylation regions (DMRs) are termed epimutations and in part transmit the transgenerational phenotypes. The agricultural fungicide vinclozolin exposure of a gestating female rat has previously been shown to promote transgenerational disease and epimutations in F3 generation (great-grand-offspring) animals. The current study was designed to investigate the actions of direct fetal exposure on the F1 generation rat sperm DMRs compared to the F3 transgenerational sperm DMRs. A protocol involving methylated DNA immunoprecipitation (MeDIP) followed by next-generation sequencing (Seq) was used in the current study. Bioinformatics analysis of the MeDIP-Seq data was developed and several different variations in the bioinformatic analysis were evaluated. Observations indicate needs to be considered. Interestingly, the F1 generation DMRs were found to be fewer in number and for the most part distinct from the F3 generation epimutations. Observations suggest the direct exposure induced F1 generation sperm DMRs appear to promote in subsequent generations alterations in the germ cell developmental programming that leads to the distinct epimutations in the F3 generation. This may help explain the differences in disease and phenotypes between the direct exposure F1 generation and transgenerational F3 generation. Observations demonstrate a distinction between the direct exposure versus transgenerational epigenetic programming induced by environmental exposures and provide insights into the molecular mechanisms involved in the epigenetic transgenerational inheritance phenomenon.
环境诱导的疾病和表型变异的表观遗传跨代遗传已被证明涉及生殖系(如精子)中的DNA甲基化改变。这些差异DNA甲基化区域(DMRs)被称为表观突变,部分传递跨代表型。先前已表明,妊娠雌性大鼠接触农业杀菌剂乙烯菌核利会促进F3代(曾孙代)动物的跨代疾病和表观突变。本研究旨在调查直接胎儿暴露对F1代大鼠精子DMRs的影响,并与F3代跨代精子DMRs进行比较。本研究采用了一种涉及甲基化DNA免疫沉淀(MeDIP)然后进行下一代测序(Seq)的方案。开发了对MeDIP-Seq数据的生物信息学分析,并评估了生物信息学分析中的几种不同变异。观察结果表明需要加以考虑。有趣的是,发现F1代DMRs的数量较少,并且在很大程度上与F3代表观突变不同。观察结果表明,直接暴露诱导的F1代精子DMRs似乎在后代中促进生殖细胞发育编程的改变,从而导致F3代出现明显的表观突变。这可能有助于解释直接暴露的F1代和跨代F3代之间疾病和表型的差异。观察结果证明了环境暴露诱导的直接暴露与跨代表观遗传编程之间的区别,并为表观遗传跨代遗传现象所涉及的分子机制提供了见解。