An Oct4‐Sall4‐Nanog network controls developmental progression in the pre‐implantation mouse embryo. Issue 1 (8th January 2013)

• Record Type: Journal Article
• Authors: Tan, Meng How; Au, Kin Fai; Leong, Denise E; Foygel, Kira; Wong, Wing H; Yao, Mylene WM
• Is Part Of: Molecular systems biology. Volume 9:Issue 1(2013)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2013-01-08
• Subjects: Molecular biology -- Periodicals; Systems biology -- Periodicals; 572.8
• DOI: 10.1038/msb.2012.65
• Languages: English
• ISSNs: 1744-4292

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Landmark events occur in a coordinated manner during pre‐implantation development of the mammalian embryo, yet the regulatory network that orchestrates these events remains largely unknown. Here, we present the first systematic investigation of the network in pre‐implantation mouse embryos using morpholino‐mediated gene knockdowns of key embryonic stem cell (ESC) factors followed by detailed transcriptome analysis of pooled embryos, single embryos, and individual blastomeres. We delineated the regulons of Oct4, Sall4, and Nanog and identified a set of metabolism‐ and transport‐related genes that were controlled by these transcription factors in embryos but not in ESCs. Strikingly, the knockdown embryos arrested at a range of developmental stages. We provided evidence that the DNA methyltransferase Dnmt3b has a role in determining the extent to which a knockdown embryo can develop. We further showed that the feed‐forward loop comprising Dnmt3b, the pluripotency factors, and the miR‐290‐295 cluster exemplifies a network motif that buffers embryos against gene expression noise. Our findings indicate that Oct4, Sall4, and Nanog form a robust and integrated network to govern mammalian pre‐implantation development.</p> </abstract>