Theunissen Thorold W, Jaenisch Rudolf
Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Development. 2017 Dec 15;144(24):4496-4509. doi: 10.1242/dev.157404.
Pluripotent stem cells have broad utility in biomedical research and their molecular regulation has thus garnered substantial interest. While the principles that establish and regulate pluripotency have been well defined in the mouse, it has been difficult to extrapolate these insights to the human system due to species-specific differences and the distinct developmental identities of mouse versus human embryonic stem cells. In this Review, we examine genome-wide approaches to elucidate the regulatory principles of pluripotency in human embryos and stem cells, and highlight where differences exist in the regulation of pluripotency in mice and humans. We review recent insights into the nature of human pluripotent cells , obtained by the deep sequencing of pre-implantation embryos. We also present an integrated overview of the principal layers of global gene regulation in human pluripotent stem cells. Finally, we discuss the transcriptional and epigenomic remodeling events associated with cell fate transitions into and out of human pluripotency.
多能干细胞在生物医学研究中具有广泛用途,因此其分子调控已引起了极大关注。虽然在小鼠中建立和调控多能性的原理已得到明确界定,但由于物种特异性差异以及小鼠与人类胚胎干细胞不同的发育特性,很难将这些见解外推至人类系统。在本综述中,我们研究了全基因组方法以阐明人类胚胎和干细胞中多能性的调控原理,并强调了小鼠和人类在多能性调控方面存在差异的地方。我们回顾了通过植入前胚胎深度测序获得的关于人类多能细胞本质的最新见解。我们还对人类多能干细胞中全局基因调控的主要层次进行了综合概述。最后,我们讨论了与人类多能性细胞命运转变相关的转录和表观基因组重塑事件。