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      Decoding the Regulatory Network for Blood Development from Single-Cell Gene Expression Measurements

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          Abstract

          Here we report the use of diffusion maps and network synthesis from state transition graphs to better understand developmental pathways from single cell gene expression profiling. We map the progression of mesoderm towards blood in the mouse by single-cell expression analysis of 3,934 cells, capturing cells with blood-forming potential at four sequential developmental stages. By adapting the diffusion plot methodology for dimensionality reduction to single-cell data, we reconstruct the developmental journey to blood at single-cell resolution. Using transitions between individual cellular states as input, we develop a single-cell network synthesis toolkit to generate a computationally executable transcriptional regulatory network model that recapitulates blood development. Model predictions were validated by showing that Sox7 inhibits primitive erythropoiesis, and that Sox and Hox factors control early expression of Erg. We therefore demonstrate that single-cell analysis of a developing organ coupled with computational approaches can reveal the transcriptional programs that control organogenesis.

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          Most cited references47

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          Genetic programs in human and mouse early embryos revealed by single-cell RNA sequencing.

          Mammalian pre-implantation development is a complex process involving dramatic changes in the transcriptional architecture. We report here a comprehensive analysis of transcriptome dynamics from oocyte to morula in both human and mouse embryos, using single-cell RNA sequencing. Based on single-nucleotide variants in human blastomere messenger RNAs and paternal-specific single-nucleotide polymorphisms, we identify novel stage-specific monoallelic expression patterns for a significant portion of polymorphic gene transcripts (25 to 53%). By weighted gene co-expression network analysis, we find that each developmental stage can be delineated concisely by a small number of functional modules of co-expressed genes. This result indicates a sequential order of transcriptional changes in pathways of cell cycle, gene regulation, translation and metabolism, acting in a step-wise fashion from cleavage to morula. Cross-species comparisons with mouse pre-implantation embryos reveal that the majority of human stage-specific modules (7 out of 9) are notably preserved, but developmental specificity and timing differ between human and mouse. Furthermore, we identify conserved key members (or hub genes) of the human and mouse networks. These genes represent novel candidates that are likely to be key in driving mammalian pre-implantation development. Together, the results provide a valuable resource to dissect gene regulatory mechanisms underlying progressive development of early mammalian embryos.
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            Causal protein-signaling networks derived from multiparameter single-cell data.

            Machine learning was applied for the automated derivation of causal influences in cellular signaling networks. This derivation relied on the simultaneous measurement of multiple phosphorylated protein and phospholipid components in thousands of individual primary human immune system cells. Perturbing these cells with molecular interventions drove the ordering of connections between pathway components, wherein Bayesian network computational methods automatically elucidated most of the traditionally reported signaling relationships and predicted novel interpathway network causalities, which we verified experimentally. Reconstruction of network models from physiologically relevant primary single cells might be applied to understanding native-state tissue signaling biology, complex drug actions, and dysfunctional signaling in diseased cells.
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              Resolution of cell fate decisions revealed by single-cell gene expression analysis from zygote to blastocyst.

              Three distinct cell types are present within the 64-cell stage mouse blastocyst. We have investigated cellular development up to this stage using single-cell expression analysis of more than 500 cells. The 48 genes analyzed were selected in part based on a whole-embryo analysis of more than 800 transcription factors. We show that in the morula, blastomeres coexpress transcription factors specific to different lineages, but by the 64-cell stage three cell types can be clearly distinguished according to their quantitative expression profiles. We identify Id2 and Sox2 as the earliest markers of outer and inner cells, respectively. This is followed by an inverse correlation in expression for the receptor-ligand pair Fgfr2/Fgf4 in the early inner cell mass. Position and signaling events appear to precede the maturation of the transcriptional program. These results illustrate the power of single-cell expression analysis to provide insight into developmental mechanisms. The technique should be widely applicable to other biological systems. Copyright 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                9604648
                20305
                Nat Biotechnol
                Nat. Biotechnol.
                Nature biotechnology
                1087-0156
                1546-1696
                27 January 2015
                09 February 2015
                March 2015
                01 September 2015
                : 33
                : 3
                : 269-276
                Affiliations
                [1 ]Department of Haematology, Cambridge Institute for Medical Research, University of Cambridge, UK
                [2 ]Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK
                [3 ]Institute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany
                [4 ]Department of Mathematics, Technische Universität München, Garching, Germany
                [5 ]Cancer Research UK Stem Cell Haematopoiesis Group, Paterson Institute for Cancer Research, University of Manchester, Manchester, UK
                [6 ]Laboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Chuo-ku, Kobe, Japan
                [7 ]Sanger Institute-EBI Single Cell Genomics Centre, Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK
                [8 ]Department of Computer Science, University of Leicester, Leicester, UK
                [9 ]Microsoft Research Cambridge, Cambridge, UK
                [10 ]Department of Biochemistry, University of Cambridge, Cambridge, UK
                Author notes
                [* ]Correspondence should be addressed to: Berthold Göttgens ( bg200@ 123456cam.ac.uk ) and Jasmin Fisher ( jasmin.fisher@ 123456microsoft.com or jf416@ 123456cam.ac.uk )

                Author Contributions

                VM, AJL, YT, ACW and ICM performed experiments and analysed data. SW, LH, FB and NP developed computational tools. WJ and ED analysed data. SN, VK, FJT, JF and BG conceived the study. VM, SW, JF and BG wrote the paper with help from all co-authors.

                Article
                EMS61867
                10.1038/nbt.3154
                4374163
                25664528
                9ec5645c-a723-4f46-9993-cd89586fdc01
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                Biotechnology
                Biotechnology

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