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dc.contributor.authorPálfy, Máté
dc.contributor.authorSchulze, Gunnar
dc.contributor.authorValen, Eivind
dc.contributor.authorVastenhouw, Nadine L.
dc.date.accessioned2021-02-12T07:54:09Z
dc.date.available2021-02-12T07:54:09Z
dc.date.created2020-10-06T12:26:57Z
dc.date.issued2020-01
dc.PublishedPLoS Genetics. 2020, 16 (1), 1-25.
dc.identifier.issn1553-7390
dc.identifier.urihttps://hdl.handle.net/11250/2727575
dc.description.abstractIn many organisms, early embryonic development is driven by maternally provided factors until the controlled onset of transcription during zygotic genome activation. The regulation of chromatin accessibility and its relationship to gene activity during this transition remain poorly understood. Here, we generated chromatin accessibility maps with ATAC-seq from genome activation until the onset of lineage specification. During this period, chromatin accessibility increases at regulatory elements. This increase is independent of RNA polymerase II-mediated transcription, with the exception of the hypertranscribed miR-430 locus. Instead, accessibility often precedes the transcription of associated genes. Loss of the maternal transcription factors Pou5f3, Sox19b, and Nanog, which are known to be required for zebrafish genome activation, results in decreased accessibility at regulatory elements. Importantly, the accessibility of regulatory regions, especially when established by Pou5f3, Sox19b and Nanog, is predictive for future transcription. Our results show that the maternally provided transcription factors Pou5f3, Sox19b, and Nanog open up chromatin and prime genes for activity during zygotic genome activation in zebrafish.en_US
dc.language.isoengen_US
dc.publisherPublic Library of Scienceen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleChromatin accessibility established by Pou5f3, Sox19b and Nanog primes genes for activity during zebrafish genome activationen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright Pa´lfy et al.en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1371/journal.pgen.1008546
dc.identifier.cristin1837555
dc.source.journalPLoS Geneticsen_US
dc.source.4016
dc.source.141
dc.source.pagenumber1-25en_US


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