Publication:
Reduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans development.

dc.contributor.authorZheleva, Angelina
dc.contributor.authorGómez-Orte, Eva
dc.contributor.authorSáenz-Narciso, Beatriz
dc.contributor.authorEzcurra, Begoña
dc.contributor.authorKassahun, Henok
dc.contributor.authorde Toro, María
dc.contributor.authorMiranda-Vizuete, Antonio
dc.contributor.authorSchnabel, Ralf
dc.contributor.authorNilsen, Hilde
dc.contributor.authorCabello, Juan
dc.date.accessioned2023-01-25T13:41:29Z
dc.date.available2023-01-25T13:41:29Z
dc.date.issued2019-09-16
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.
dc.identifier.doi10.1371/journal.pgen.1008338
dc.identifier.essn1553-7404
dc.identifier.pmcPMC6762213
dc.identifier.pmid31525188
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6762213/pdf
dc.identifier.unpaywallURLhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1008338&type=printable
dc.identifier.urihttp://hdl.handle.net/10668/14510
dc.issue.number9
dc.journal.titlePLoS genetics
dc.journal.titleabbreviationPLoS Genet
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.numbere1008338
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshActive Transport, Cell Nucleus
dc.subject.meshAmino Acid Sequence
dc.subject.meshAnimals
dc.subject.meshCaenorhabditis elegans
dc.subject.meshCaenorhabditis elegans Proteins
dc.subject.meshCell Nucleus
dc.subject.meshCytoplasm
dc.subject.meshNucleocytoplasmic Transport Proteins
dc.subject.meshOrgan Specificity
dc.subject.meshRNA Transport
dc.subject.meshRNA, Messenger
dc.subject.meshRNA-Binding Proteins
dc.titleReduction of mRNA export unmasks different tissue sensitivities to low mRNA levels during Caenorhabditis elegans development.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number15
dspace.entity.typePublication

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