White Carlee R, MacDonald William A, Mann Mellissa R W
Department of Obstetrics and Gynecology, University of Western Ontario, Schulich School of Medicine and Dentistry, London, Ontario, Canada Department of Biochemistry, University of Western Ontario, Schulich School of Medicine and Dentistry, London, Ontario, Canada Children's Health Research Institute, London, Ontario, Canada.
Magee-Womens Research Institute, Pittsburgh, Pennsylvania Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Biol Reprod. 2016 Sep;95(3):61. doi: 10.1095/biolreprod.116.140319. Epub 2016 Jul 27.
In mice, assisted reproductive technologies (ARTs) applied during gametogenesis and preimplantation development can result in disruption of genomic imprinting. In humans, these technologies and/or subfertility have been linked to perturbations in genomic imprinting. To understand how ARTs and infertility affect DNA methylation, it is important to understand DNA methylation dynamics and the role of regulatory factors at these critical stages. Recent genome studies performed using mouse and human gametes and preimplantation embryos have shed light onto these processes. Here, we comprehensively review the current state of knowledge regarding global and imprinted DNA methylation programming in the mouse and human. Available data highlight striking similarities in mouse and human DNA methylation dynamics during gamete and preimplantation development. Just as fascinating, these studies have revealed sex-, gene-, and allele-specific differences in DNA methylation programming, warranting future investigation to untangle the complex regulation of DNA methylation dynamics during gamete and preimplantation development.
在小鼠中,配子发生和植入前发育过程中应用的辅助生殖技术(ARTs)可导致基因组印记的破坏。在人类中,这些技术和/或生育力低下与基因组印记的扰动有关。为了了解ARTs和不孕症如何影响DNA甲基化,了解这些关键阶段的DNA甲基化动态以及调控因子的作用非常重要。最近使用小鼠和人类配子及植入前胚胎进行的基因组研究揭示了这些过程。在这里,我们全面回顾了关于小鼠和人类全基因组及印记DNA甲基化编程的当前知识状态。现有数据突出了小鼠和人类配子及植入前发育过程中DNA甲基化动态的惊人相似之处。同样引人入胜的是,这些研究揭示了DNA甲基化编程中的性别、基因和等位基因特异性差异,这需要未来进行研究以理清配子和植入前发育过程中DNA甲基化动态的复杂调控。