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10.7554/eLife.23588

http://scihub22266oqcxt.onion/10.7554/eLife.23588
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C5391207!5391207!28323620
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suck abstract from ncbi


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pmid28323620      eLife 2017 ; 6 (ä): ä
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  • Discovery of novel determinants of endothelial lineage using chimeric heterokaryons #MMPMID28323620
  • Wong WT; Matrone G; Tian X; Tomoiaga SA; Au KF; Meng S; Yamazoe S; Sieveking D; Chen K; Burns DM; Chen JK; Blau HM; Cooke JP
  • eLife 2017[]; 6 (ä): ä PMID28323620show ga
  • We wish to identify determinants of endothelial lineage. Murine embryonic stem cells (mESC) were fused with human endothelial cells in stable, non-dividing, heterokaryons. Using RNA-seq, it is possible to discriminate between human and mouse transcripts in these chimeric heterokaryons. We observed a temporal pattern of gene expression in the ESCs of the heterokaryons that recapitulated ontogeny, with early mesodermal factors being expressed before mature endothelial genes. A set of transcriptional factors not known to be involved in endothelial development was upregulated, one of which was POU class 3 homeobox 2 (Pou3f2). We confirmed its importance in differentiation to endothelial lineage via loss- and gain-of-function (LOF and GOF). Its role in vascular development was validated in zebrafish embryos using morpholino oligonucleotides. These studies provide a systematic and mechanistic approach for identifying key regulators in directed differentiation of pluripotent stem cells to somatic cell lineages.DOI:http://dx.doi.org/10.7554/eLife.23588.001
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