Ma Haixia, Lin Yu, Zhao Zhen-Ao, Lu Xukun, Yu Yang, Zhang Xiaoxin, Wang Qiang, Li Lei
From the State Key Laboratory of Stem Cell and Reproductive Biology and the Institute of Zoology, University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, 100101 Beijing and.
J Biol Chem. 2016 Jun 3;291(23):12126-35. doi: 10.1074/jbc.M116.723247. Epub 2016 Apr 12.
Specification of the three germ layers is a fundamental process and is essential for the establishment of organ rudiments. Multiple genetic and epigenetic factors regulate this dynamic process; however, the function of specific microRNAs in germ layer differentiation remains unknown. In this study, we established that microRNA-127 (miR-127) is related to germ layer specification via microRNA array analysis of isolated three germ layers of E7.5 mouse embryos and was verified through differentiation of mouse embryonic stem cells. miR-127 is highly expressed in endoderm and primitive streak. Overexpression of miR-127 increases and inhibition of miR-127 decreases the expression of mesendoderm markers. We further show that miR-127 promotes mesendoderm differentiation through the nodal pathway, a determinative signaling pathway in early embryogenesis. Using luciferase reporter assay, left-right determination factor 2 (Lefty2), an antagonist of nodal, is identified to be a novel target of miR-127. Furthermore, the role of miR-127 in mesendoderm differentiation is attenuated by Lefty2 overexpression. Altogether, our results indicate that miR-127 accelerates mesendoderm differentiation of mouse embryonic stem cells through nodal signaling by targeting Lefty2.
三胚层的特化是一个基本过程,对于器官原基的建立至关重要。多种遗传和表观遗传因素调节这一动态过程;然而,特定微小RNA在胚层分化中的功能仍不清楚。在本研究中,我们通过对E7.5小鼠胚胎分离出的三个胚层进行微小RNA阵列分析,确定微小RNA-127(miR-127)与胚层特化有关,并通过小鼠胚胎干细胞的分化进行了验证。miR-127在内胚层和原条中高度表达。miR-127的过表达增加,而miR-127的抑制降低了中内胚层标志物的表达。我们进一步表明,miR-127通过节点途径促进中内胚层分化,节点途径是早期胚胎发育中的决定性信号通路。使用荧光素酶报告基因测定法,确定节点的拮抗剂左右决定因子2(Lefty2)是miR-127的一个新靶点。此外,Lefty2的过表达减弱了miR-127在中内胚层分化中的作用。总之,我们的结果表明,miR-127通过靶向Lefty2,通过节点信号加速小鼠胚胎干细胞的中内胚层分化。