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      Anteroposterior polarity and elongation in the absence of extra-embryonic tissues and of spatially localised signalling in gastruloids: mammalian embryonic organoids

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          Abstract

          The establishment of the anteroposterior (AP) axis is a crucial step during animal embryo development. In mammals, genetic studies have shown that this process relies on signals spatiotemporally deployed in the extra-embryonic tissues that locate the position of the head and the onset of gastrulation, marked by T/Brachyury ( T/Bra) at the posterior of the embryo. Here, we use gastruloids, mESC-based organoids, as a model system with which to study this process. We find that gastruloids localise T/Bra expression to one end and undergo elongation similar to the posterior region of the embryo, suggesting that they develop an AP axis. This process relies on precisely timed interactions between Wnt/β-catenin and Nodal signalling, whereas BMP signalling is dispensable. Additionally, polarised T/Bra expression occurs in the absence of extra-embryonic tissues or localised sources of signals. We suggest that the role of extra-embryonic tissues in the mammalian embryo might not be to induce the axes but to bias an intrinsic ability of the embryo to initially break symmetry. Furthermore, we suggest that Wnt signalling has a separable activity involved in the elongation of the axis.

          Abstract

          [Related article:] Highlighted Article: Early gastruloid patterning involves the development of the embryonic axes in the absence of extra-embryonic tissues, a process that relies on the interactions of Nodal and Wnt, but not BMP.

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          Most cited references69

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          Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling.

          The stability of the Wnt pathway transcription factor beta-catenin is tightly regulated by the multi-subunit destruction complex. Deregulated Wnt pathway activity has been implicated in many cancers, making this pathway an attractive target for anticancer therapies. However, the development of targeted Wnt pathway inhibitors has been hampered by the limited number of pathway components that are amenable to small molecule inhibition. Here, we used a chemical genetic screen to identify a small molecule, XAV939, which selectively inhibits beta-catenin-mediated transcription. XAV939 stimulates beta-catenin degradation by stabilizing axin, the concentration-limiting component of the destruction complex. Using a quantitative chemical proteomic approach, we discovered that XAV939 stabilizes axin by inhibiting the poly-ADP-ribosylating enzymes tankyrase 1 and tankyrase 2. Both tankyrase isoforms interact with a highly conserved domain of axin and stimulate its degradation through the ubiquitin-proteasome pathway. Thus, our study provides new mechanistic insights into the regulation of axin protein homeostasis and presents new avenues for targeted Wnt pathway therapies.
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            Conversion of embryonic stem cells into neuroectodermal precursors in adherent monoculture.

            Mouse embryonic stem (ES) cells are competent for production of all fetal and adult cell types. However, the utility of ES cells as a developmental model or as a source of defined cell populations for pharmaceutical screening or transplantation is compromised because their differentiation in vitro is poorly controlled. Specification of primary lineages is not understood and consequently differentiation protocols are empirical, yielding variable and heterogeneous outcomes. Here we report that neither multicellular aggregation nor coculture is necessary for ES cells to commit efficiently to a neural fate. In adherent monoculture, elimination of inductive signals for alternative fates is sufficient for ES cells to develop into neural precursors. This process is not a simple default pathway, however, but requires autocrine fibroblast growth factor (FGF). Using flow cytometry quantitation and recording of individual colonies, we establish that the bulk of ES cells undergo neural conversion. The neural precursors can be purified to homogeneity by fluorescence activated cell sorting (FACS) or drug selection. This system provides a platform for defining the molecular machinery of neural commitment and optimizing the efficiency of neuronal and glial cell production from pluripotent mammalian stem cells.
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              Gene function in mouse embryogenesis: get set for gastrulation.

              During early mouse embryogenesis, temporal and spatial regulation of gene expression and cell signalling influences lineage specification, embryonic polarity, the patterning of tissue progenitors and the morphogenetic movement of cells and tissues. Uniquely in mammals, the extraembryonic tissues are the source of signals for lineage specification and tissue patterning. Here we discuss recent discoveries about the lead up to gastrulation, including early manifestations of asymmetry, coordination of cell and tissue movements and the interactions of transcription factors and signalling activity for lineage allocation and germ-layer specification.
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                Author and article information

                Journal
                Development
                Development
                DEV
                develop
                Development (Cambridge, England)
                The Company of Biologists Ltd
                0950-1991
                1477-9129
                1 November 2017
                1 November 2017
                : 144
                : 21
                : 3894-3906
                Affiliations
                [1 ]Department of Genetics, University of Cambridge , Downing Street, Cambridge CB2 3EH, UK
                [2 ]Laboratory of Stem Cell Bioengineering, Institute of Bioengineering, School of Life Sciences and School of Engineering, École Polytechnique Fédérale de Lausanne , 1015 Lausanne, Switzerland
                [3 ]Wellcome Trust-Medical Research Council Stem Cell Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK
                [4 ]Université Paris-Diderot, CNRS, Institut Jacques Monod, 75013 Paris, France
                [5 ]Danish Stem Cell Center, University of Copenhagen , DK-2200 Copenhagen, Denmark
                Author notes
                [* ]Authors for correspondence ( dat40@ 123456cam.ac.uk ; ama11@ 123456cam.ac.uk )
                Author information
                http://orcid.org/0000-0002-3447-7662
                http://orcid.org/0000-0003-0953-0553
                http://orcid.org/0000-0003-2157-5017
                http://orcid.org/0000-0001-7838-839X
                http://orcid.org/0000-0002-1781-564X
                Article
                DEV150391
                10.1242/dev.150391
                5702072
                28951435
                d2857df9-0137-4d39-97ad-f0cee6f95c45
                © 2017. Published by The Company of Biologists Ltd

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 13 February 2017
                : 8 September 2017
                Funding
                Funded by: European Research Council, http://dx.doi.org/10.13039/100010663;
                Award ID: 250316
                Funded by: Biotechnology and Biological Sciences Research Council, http://dx.doi.org/10.13039/501100000268;
                Award ID: BB/M023370/1
                Funded by: National Centre for the Replacement, Refinement and Reduction of Animals in Research, http://dx.doi.org/10.13039/501100000849;
                Award ID: NC/P001467/1
                Funded by: Herchel Smith Fund;
                Funded by: Engineering and Physical Sciences Research Council;
                Funded by: École Polytechnique Fédérale de Lausanne, http://dx.doi.org/10.13039/501100001703;
                Funded by: Wellcome Trust, http://dx.doi.org/10.13039/100004440;
                Award ID: 109408/Z/15/Z
                Funded by: Royal Society, http://dx.doi.org/10.13039/501100000288;
                Award ID: 109408/Z/15/Z
                Funded by: Company of Biologists, http://dx.doi.org/10.13039/501100000522;
                Award ID: DEVTF-151210
                Categories
                203
                Stem Cells and Regeneration

                Developmental biology
                gastruloids,axial organisation,organoids,symmetry-breaking
                Developmental biology
                gastruloids, axial organisation, organoids, symmetry-breaking

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