Paikari Alireza, D Belair Cassandra, Saw Daniel, Blelloch Robert
The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Center for Reproductive Sciences, University of California, San Francisco, San Francisco, CA 94143, USA.
Department of Urology, University of California, San Francisco, CA 94143, USA.
Development. 2017 Oct 15;144(20):3731-3743. doi: 10.1242/dev.151654. Epub 2017 Sep 21.
The vertebrate-specific ESCC microRNA family arises from two genetic loci in mammals: miR-290/miR-371 and miR-302. The miR-302 locus is found broadly among vertebrates, whereas the miR-290/miR-371 locus is unique to eutheria, suggesting a role in placental development. Here, we evaluate that role. A knock-in reporter for the mouse miR-290 cluster is expressed throughout the embryo until gastrulation, when it becomes specifically expressed in extraembryonic tissues and the germline. In the placenta, expression is limited to the trophoblast lineage, where it remains highly expressed until birth. Deletion of the miR-290 cluster gene () results in reduced trophoblast progenitor cell proliferation and a reduced DNA content in endoreduplicating trophoblast giant cells. The resulting placenta is reduced in size. In addition, the vascular labyrinth is disorganized, with thickening of the maternal-fetal blood barrier and an associated reduction in diffusion. Multiple mRNA targets of the miR-290 cluster microRNAs are upregulated. These data uncover a crucial function for the miR-290 cluster in the regulation of a network of genes required for placental development, suggesting a central role for these microRNAs in the evolution of placental mammals.
脊椎动物特有的食管鳞状细胞癌微小RNA家族起源于哺乳动物的两个基因位点:miR - 290/miR - 371和miR - 302。miR - 302基因位点在脊椎动物中广泛存在,而miR - 290/miR - 371基因位点是真兽亚纲动物所特有的,这表明其在胎盘发育中发挥作用。在此,我们评估这一作用。小鼠miR - 290簇的一个敲入报告基因在整个胚胎中表达,直到原肠胚形成期,此时它在胚外组织和生殖系中特异性表达。在胎盘中,表达仅限于滋养层谱系,在那里它一直高度表达直至出生。删除miR - 290簇基因()会导致滋养层祖细胞增殖减少以及内复制滋养层巨细胞中的DNA含量降低。所形成的胎盘尺寸减小。此外,血管迷路紊乱,母胎血屏障增厚且扩散相关功能降低。miR - 290簇微小RNA的多个mRNA靶标上调。这些数据揭示了miR - 290簇在调控胎盘发育所需基因网络中的关键功能,表明这些微小RNA在胎盘哺乳动物进化中起核心作用。