Yan Wei
Department of Physiology and Cell Biology, University of Nevada School of Medicine, 1664 North Virginia Street, MS575, Reno, NV 89557, USA.
Mol Cell Endocrinol. 2014 Dec;398(1-2):24-30. doi: 10.1016/j.mce.2014.09.008. Epub 2014 Sep 16.
"Epigenetic transgenerational inheritance" (ETI) has been defined as germline (sperm or egg) transmission of epigenetic information between generations in the absence of direct exposures or genetic manipulations. Among reported cases of ETI in mammals, the majority are induced by environmental factors, including environmental toxicants [e.g. agricultural fungicide vinclozolin, plastic additive bisphenol A, pesticide methoxychlor, dioxin, di-(2-ethylhexyl) phthalate, dichlorodiphenyltrichloroethane, and hydrocarbons] and poor nutritional conditions. Although the ETI phenomenon is well established, the underlying mechanism remains elusive. Putative epimutations, including changes in DNA methylation and histone modification patterns, have been reported, but it remains unclear how these epimutations are formed in the first place, and how they are memorized in the germline and then get transmitted to subsequent generations. Based on recent advances in our understanding of regulatory noncoding RNAs (ncRNAs), I propose that ncRNAs are involved in ETI, during both the initial epimutation formation and the subsequent germline transmission of epimutations. ncRNAs can function at epigenetic levels by affecting DNA methylation and histone modifications, thereby changing gene transcriptional activities, which can lead to an altered mRNA transcriptome associated with a disease phenotype. Alternatively, novel or altered ncRNA expression can cause dysregulated post-transcriptional regulation, thus directly affecting the mRNA transcriptome and inducing a disease phenotype. Sperm-borne ncRNAs are potential mediators for epigenetic memory across generations, but they alone may not be sufficient for stable transmission of epimutations across generations. Overall, research on ncRNAs in the context of ETI is urgently needed to shed light on the underlying mechanism of ETI.
“表观遗传跨代遗传”(ETI)被定义为在无直接暴露或基因操作的情况下,表观遗传信息在代际间通过生殖细胞(精子或卵子)进行传递。在已报道的哺乳动物ETI案例中,大多数是由环境因素诱导的,包括环境毒物[如农用杀菌剂乙烯菌核利、塑料添加剂双酚A、杀虫剂甲氧滴滴涕、二噁英、邻苯二甲酸二(2-乙基己基)酯、滴滴涕和碳氢化合物]以及不良营养状况。尽管ETI现象已得到充分证实,但其潜在机制仍不清楚。已报道了一些推定的表观突变,包括DNA甲基化和组蛋白修饰模式的变化,但这些表观突变最初是如何形成的,以及它们如何在生殖细胞中被记忆并随后传递给后代仍不清楚。基于我们对调控性非编码RNA(ncRNA)理解的最新进展,我提出ncRNA参与了ETI过程,包括初始表观突变的形成以及随后表观突变在生殖细胞中的传递。ncRNA可通过影响DNA甲基化和组蛋白修饰在表观遗传水平发挥作用,从而改变基因转录活性,这可能导致与疾病表型相关的mRNA转录组发生改变。或者,新的或改变的ncRNA表达可导致转录后调控失调,从而直接影响mRNA转录组并诱导疾病表型。精子携带的ncRNA是跨代表观遗传记忆的潜在介质,但它们单独可能不足以实现表观突变在代际间的稳定传递。总体而言,迫切需要在ETI背景下对ncRNA进行研究,以阐明ETI的潜在机制。