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dc.contributor.authorGialitakis, M
dc.contributor.authorTolaini, M
dc.contributor.authorLi, Y
dc.contributor.authorPardo, M
dc.contributor.authorYu, L
dc.contributor.authorToribio, A
dc.contributor.authorChoudhary, JS
dc.contributor.authorNiakan, K
dc.contributor.authorPapayannopoulos, V
dc.contributor.authorStockinger, B
dc.date.accessioned2020-06-15T10:35:34Z
dc.date.issued2017-10-01
dc.identifier.citationStem cell reports, 2017, 9 (5), pp. 1377 - 1386
dc.identifier.issn2213-6711
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3736
dc.identifier.eissn2213-6711
dc.identifier.doi10.1016/j.stemcr.2017.09.025
dc.description.abstractThe transcriptional program of early embryonic development is tightly regulated by a set of well-defined transcription factors that suppress premature expression of differentiation genes and sustain the pluripotent identity. It is generally accepted that this program can be perturbed by environmental factors such as chemical pollutants; however, the precise molecular mechanisms remain unknown. The aryl hydrocarbon receptor (AHR) is a widely expressed nuclear receptor that senses environmental stimuli and modulates target gene expression. Here, we have investigated the AHR interactome in embryonic stem cells by mass spectrometry and show that ectopic activation of AHR during early differentiation disrupts the differentiation program via the chromatin remodeling complex NuRD (nucleosome remodeling and deacetylation). The activated AHR/NuRD complex altered the expression of differentiation-specific genes that control the first two developmental decisions without affecting the pluripotency program. These findings identify a mechanism that allows environmental stimuli to disrupt embryonic development through AHR signaling.
dc.formatPrint-Electronic
dc.format.extent1377 - 1386
dc.languageeng
dc.language.isoeng
dc.publisherCELL PRESS
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectPluripotent Stem Cells
dc.subjectAnimals
dc.subjectMice, Inbred C57BL
dc.subjectMice
dc.subjectReceptors, Aryl Hydrocarbon
dc.subjectCell Differentiation
dc.subjectGene Expression Regulation, Developmental
dc.subjectEmbryonic Development
dc.subjectMi-2 Nucleosome Remodeling and Deacetylase Complex
dc.subjectProtein Interaction Maps
dc.subjectMouse Embryonic Stem Cells
dc.titleActivation of the Aryl Hydrocarbon Receptor Interferes with Early Embryonic Development.
dc.typeJournal Article
dcterms.dateAccepted2017-09-28
rioxxterms.versionofrecord10.1016/j.stemcr.2017.09.025
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-11
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfStem cell reports
pubs.issue5
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Functional Proteomics Group
pubs.publication-statusPublished
pubs.volume9
pubs.embargo.termsNot known
icr.researchteamFunctional Proteomics Group
dc.contributor.icrauthorPardo Calvo, Maria Mercedes
dc.contributor.icrauthorChoudhary, Jyoti


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