Wu Guangming, Lei Lei, Schöler Hans R
Department of Cell and Developmental Biology, Max Planck Institute for Molecular Biomedicine, Röntgenstrasse 20, 48149, Münster, Germany.
Department of Histology and Embryology, Harbin Medical University, 194 Xuefu Road, Nangang District, Harbin, 150081, China.
J Mol Med (Berl). 2017 Jul;95(7):687-694. doi: 10.1007/s00109-017-1509-5. Epub 2017 Jan 19.
In mammals, the unicellular zygote starts the process of embryogenesis and differentiates into all types of somatic cells, including both fetal and extraembryonic lineages-in a highly organized manner to eventually give rise to an entire multicellular organism comprising more than 200 different tissue types. This feature is referred to as totipotency. Upon fertilization, oocyte maternal factors epigenetically reprogram the genomes of the terminally differentiated oocyte and spermatozoon and turn the zygote into a totipotent cell. Today, we still do not fully understand the molecular properties of totipotency. In this review, we discuss recent findings on the molecular signature and mechanism of transcriptional regulation networks in the totipotent mouse embryo.
在哺乳动物中,单细胞受精卵启动胚胎发生过程,并以高度有序的方式分化为所有类型的体细胞,包括胎儿和胚外谱系,最终发育成一个由200多种不同组织类型组成的完整多细胞生物体。这一特性被称为全能性。受精后,卵母细胞的母体因子对终末分化的卵母细胞和精子的基因组进行表观遗传重编程,将受精卵转变为全能细胞。如今,我们仍未完全了解全能性的分子特性。在这篇综述中,我们讨论了关于全能小鼠胚胎中转录调控网络的分子特征和机制的最新研究发现。