| Literature DB >> 27404362 |
Jens Durruthy-Durruthy1, Mark Wossidlo2, Sunil Pai3, Yusuke Takahashi4, Gugene Kang3, Larsson Omberg5, Bertha Chen3, Hiromitsu Nakauchi4, Renee Reijo Pera6, Vittorio Sebastiano7.
Abstract
Human preimplantation embryo development involves complex cellular and molecular events that lead to the establishment of three cell lineages in the blastocyst: trophectoderm, primitive endoderm, and epiblast. Owing to limited resources of biological specimens, our understanding of how the earliest lineage commitments are regulated remains narrow. Here, we examined gene expression in 241 individual cells from early and late human blastocysts to delineate dynamic gene-expression changes. We distinguished all three lineages and further developed a 3D model of the inner cell mass and trophectoderm in which individual cells were mapped into distinct expression domains. We identified in silico precursors of the epiblast and primitive endoderm lineages and revealed a role for MCRS1, TET1, and THAP11 in epiblast formation and their ability to induce naive pluripotency in vitro. Our results highlight the potential of single-cell gene-expression analysis in human preimplantation development to instruct human stem cell biology. Published by Elsevier Inc.Entities:
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Year: 2016 PMID: 27404362 DOI: 10.1016/j.devcel.2016.06.014
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270