首页> 美国卫生研究院文献>Environmental Epigenetics >Generational comparisons (F1 versus F3) of vinclozolin induced epigenetic transgenerational inheritance of sperm differential DNA methylation regions (epimutations) using MeDIP-Seq
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Generational comparisons (F1 versus F3) of vinclozolin induced epigenetic transgenerational inheritance of sperm differential DNA methylation regions (epimutations) using MeDIP-Seq

机译:使用MeDIP-Seq对Vinclozolin诱导的精子差异DNA甲基化区域(表位突变)的​​表观遗传转基因遗传世代比较(F1与F3)

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摘要

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.
机译:已证明环境诱导的疾病的表观遗传跨代遗传和表型变异涉及种系(例如精子)中的DNA甲基化改变。这些差异DNA甲基化区域(DMR)被称为表位突变,并部分传递跨代表型。先前已证明,妊娠雌性大鼠的农用杀菌剂长春新唑林暴露可促进F3代(大后代)动物的转基因疾病和表观突变。当前的研究旨在调查与F3代精子DMR相比,直接胎儿暴露对F1代大鼠精子DMR的作用。在本研究中,使用了涉及甲基化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体。观察表明需要考虑。有趣的是,发现F1代DMR的数量较少,并且在大多数情况下与F3代突变不同。观察结果表明,直接暴露诱导的F1代精子DMR似乎在随后的世代中促进生殖细胞发育程序的改变,从而导致F3代中的明显表位变异。这可能有助于解释直接暴露的F1代和跨世代的F3代之间疾病和表型的差异。观察结果表明环境暴露引起的直接暴露与后代表观遗传编程之间的区别,并提供了对表观遗传跨代遗传现象涉及的分子机制的见解。

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