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dc.date.accessioned2020-06-11T19:04:11Z
dc.date.available2020-06-11T19:04:11Z
dc.date.created2019-11-24T17:50:01Z
dc.date.issued2019
dc.identifier.citationZheleva, Angelina Gómez-Orte, Eva Sáenz-Narciso, Beatriz Ezcurra, Begoña Kassahun, Henok de Toro, María Miranda-Vizuete, Antonio Schnabel, Ralf Nilsen, Hilde Cabello, Juan . Reduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans development. PLoS Genetics. 2019, 15:e1008338(9), 1-33
dc.identifier.urihttp://hdl.handle.net/10852/76907
dc.description.abstractAnimal development requires the execution of specific transcriptional programs in different sets of cells to build tissues and functional organs. Transcripts are exported from the nucleus to the cytoplasm where they are translated into proteins that, ultimately, carry out the cellular functions. Here we show that in Caenorhabditis elegans, reduction of mRNA export strongly affects epithelial morphogenesis and germline proliferation while other tissues remain relatively unaffected. Epithelialization and gamete formation demand a large number of transcripts in the cytoplasm for the duration of these processes. In addition, our findings highlight the existence of a regulatory feedback mechanism that activates gene expression in response to low levels of cytoplasmic mRNA. We expand the genetic characterization of nuclear export factor NXF-1 to other members of the mRNA export pathway to model mRNA export and recycling of NXF-1 back to the nucleus. Our model explains how mutations in genes involved in general processes, such as mRNA export, may result in tissue-specific developmental phenotypes.en_US
dc.languageEN
dc.publisherPublic Library of Science (PLoS)
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleReduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans developmenten_US
dc.typeJournal articleen_US
dc.creator.authorZheleva, Angelina
dc.creator.authorGómez-Orte, Eva
dc.creator.authorSáenz-Narciso, Beatriz
dc.creator.authorEzcurra, Begoña
dc.creator.authorKassahun, Henok
dc.creator.authorde Toro, María
dc.creator.authorMiranda-Vizuete, Antonio
dc.creator.authorSchnabel, Ralf
dc.creator.authorNilsen, Hilde
dc.creator.authorCabello, Juan
cristin.unitcode185,53,82,10
cristin.unitnameAvdeling for klinisk molekylærbiologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1751505
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS Genetics&rft.volume=15:e1008338&rft.spage=1&rft.date=2019
dc.identifier.jtitlePLoS Genetics
dc.identifier.volume15
dc.identifier.issue9
dc.identifier.doihttps://doi.org/10.1371/journal.pgen.1008338
dc.identifier.urnURN:NBN:no-80002
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1553-7390
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/76907/1/journal.pgen.1008338.pdf
dc.type.versionPublishedVersion
cristin.articleide1008338


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