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dc.contributor.authorManning, Cerys S.
dc.contributor.authorBiga, Veronica
dc.contributor.authorBoyd, James
dc.contributor.authorKursawe, Jochen
dc.contributor.authorYmisson, Bodvar
dc.contributor.authorSpiller, David G.
dc.contributor.authorSanderson, Christopher M.
dc.contributor.authorGalla, Tobias
dc.contributor.authorRattray, Magnus
dc.contributor.authorPapalopulu, Nancy
dc.date.accessioned2019-08-08T14:30:07Z
dc.date.available2019-08-08T14:30:07Z
dc.date.issued2019-06-27
dc.identifier.citationManning , C S , Biga , V , Boyd , J , Kursawe , J , Ymisson , B , Spiller , D G , Sanderson , C M , Galla , T , Rattray , M & Papalopulu , N 2019 , ' Quantitative single-cell live imaging links HES5 dynamics with cell-state and fate in murine neurogenesis ' , Nature Communications , vol. 10 , 2835 . https://doi.org/10.1038/s41467-019-10734-8en
dc.identifier.issn2041-1723
dc.identifier.otherPURE: 260459442
dc.identifier.otherPURE UUID: b1d82ea0-4f23-4045-a14d-c099c241f5c3
dc.identifier.otherPubMed: 31249377
dc.identifier.otherPubMedCentral: PMC6597611
dc.identifier.otherScopus: 85068080331
dc.identifier.otherORCID: /0000-0002-0314-9623/work/60427778
dc.identifier.urihttp://hdl.handle.net/10023/18276
dc.descriptionFunding: V.B. and J.K. were supported by a Wellcome Trust Senior Research Fellowship to N.P. (090868/Z/09/Z)en
dc.description.abstractDuring embryogenesis cells make fate decisions within complex tissue environments. The levels and dynamics of transcription factor expression regulate these decisions. Here, we use single cell live imaging of an endogenous HES5 reporter and absolute protein quantification to gain a dynamic view of neurogenesis in the embryonic mammalian spinal cord. We report that dividing neural progenitors show both aperiodic and periodic HES5 protein fluctuations. Mathematical modelling suggests that in progenitor cells the HES5 oscillator operates close to its bifurcation boundary where stochastic conversions between dynamics are possible. HES5 expression becomes more frequently periodic as cells transition to differentiation which, coupled with an overall decline in HES5 expression, creates a transient period of oscillations with higher fold expression change. This increases the decoding capacity of HES5 oscillations and correlates with interneuron versus motor neuron cell fate. Thus, HES5 undergoes complex changes in gene expression dynamics as cells differentiate.
dc.format.extent19
dc.language.isoeng
dc.relation.ispartofNature Communicationsen
dc.rights© The Author(s) 2019. This article is licensed under a Creative CommonsAttribution 4.0 International License, which permits use, sharing,adaptation, distribution and reproduction in any medium or format, as long as you giveappropriate credit to the original author(s) and the source, provide a link to the CreativeCommons license, and indicate if changes were made. The images or other third partymaterial in this article are included in the article’s Creative Commons license, unlessindicated otherwise in a credit line to the material. If material is not included in thearticle’s Creative Commons license and your intended use is not permitted by statutoryregulation or exceeds the permitted use, you will need to obtain permission directly fromthe copyright holder. To view a copy of this license, visithttp://creativecommons.org/licenses/by/4.0/en
dc.subjectQA Mathematicsen
dc.subjectQH301 Biologyen
dc.subjectDASen
dc.subjectBDCen
dc.subject.lccQAen
dc.subject.lccQH301en
dc.titleQuantitative single-cell live imaging links HES5 dynamics with cell-state and fate in murine neurogenesisen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.Applied Mathematicsen
dc.identifier.doihttps://doi.org/10.1038/s41467-019-10734-8
dc.description.statusPeer revieweden


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