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dc.contributor.authorNichols, J
dc.contributor.authorMulas, Carla
dc.contributor.authorHodgson, Andrew
dc.contributor.authorStirparo, Giuliano
dc.date.accessioned2018-09-27T14:09:18Z
dc.date.available2018-09-27T14:09:18Z
dc.date.issued2018-06-18
dc.identifier.issn0950-1991
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/282773
dc.description.abstractLineage segregation in the mouse embryo is a finely controlled process dependent upon coordination of signalling pathways and transcriptional responses. Here we employ a conditional deletion system to investigate embryonic patterning and lineage specification in response to loss of Oct4. We first observe ectopic expression of Nanog in Oct4-negative postimplantation epiblast cells. The expression domains of lineage markers are subsequently disrupted. Definitive endoderm expands at the expense of mesoderm; the anterior/posterior axis is positioned more distally and an ectopic posterior-like domain appears anteriorly, suggesting a role for Oct4 in maintaining the embryonic axis. Although primitive streak forms in the presumptive proximal-posterior region, epithelial-to mesenchymal transition is impeded by an increase of E-cadherin, leading to complete tissue disorganisation and failure to generate germ layers. In explant and in vitro differentiation assays, Oct4 mutants also show upregulation of E-cadherin and Foxa2, suggesting a cell-autonomous phenotype. We confirm requirement for Oct4 in self-renewal of postimplantation epiblast ex vivo. Our results indicate a role for Oct4 in orchestrating multiple fates and enabling expansion, correct patterning and lineage choice in the post-implantation epiblast.
dc.description.sponsorshipThis work was supported by the Wellcome Trust, Biotechnology and Biological Sciences Research Council, Medical Research Council and the University of Cambridge. The Cambridge Stem Cell Institute is supported by core funding from the Wellcome Trust and Medical Research Council.
dc.publisherThe Company of Biologists
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectStemCellInstitute
dc.titleOct4 regulates the embryonic axis and coordinates exit from pluripotency 2 and germ layer specification in the mouse embryo
dc.typeArticle
prism.endingPage1
prism.issueIdentifier12
prism.publicationNameDevelopment
prism.startingPage1
prism.volume145
dc.identifier.doi10.17863/CAM.30137
dcterms.dateAccepted2018-05-08
rioxxterms.versionofrecord10.1242/dev.159103
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2018-05-08
dc.contributor.orcidNichols, Jennifer [0000-0002-8650-1388]
dc.contributor.orcidMulas, Carla [0000-0002-9492-6482]
dc.contributor.orcidStirparo, Giuliano [0000-0002-5911-8682]
dc.identifier.eissn1477-9129
rioxxterms.typeJournal Article/Review
pubs.funder-project-idMedical Research Council (MC_PC_12009)
cam.issuedOnline2018-06-18


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International