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dc.date.accessioned2018-08-31T10:48:34Z
dc.date.available2018-08-31T10:48:34Z
dc.date.created2018-01-24T11:05:09Z
dc.date.issued2017
dc.identifier.citationAntoniali, Giulia Serra, Fabrizio Lirussi, Lisa Tanaka, Mikiei D'Ambrosio, Chiara Zhang, Shiheng Radovic, Slobodanka Dalla, Emiliano Ciani, Yari Scaloni, Andrea Li, Mengxia Piazza, Silvano Tell, Gianluca . Mammalian APE1 controls miRNA processing and its interactome is linked to cancer RNA metabolism. Nature Communications. 2017, 8(1)
dc.identifier.urihttp://hdl.handle.net/10852/64028
dc.description.abstractMammalian apurinic/apyrimidinic endonuclease 1 is a DNA repair enzyme involved in genome stability and expression of genes involved in oxidative stress responses, tumor progression and chemoresistance. However, the molecular mechanisms underlying the role of apurinic/apyrimidinic endonuclease 1 in these processes are still unclear. Recent findings point to a novel role of apurinic/apyrimidinic endonuclease 1 in RNA metabolism. Through the characterization of the interactomes of apurinic/apyrimidinic endonuclease 1 with RNA and other proteins, we demonstrate here a role for apurinic/apyrimidinic endonuclease 1 in pri-miRNA processing and stability via association with the DROSHA-processing complex during genotoxic stress. We also show that endonuclease activity of apurinic/apyrimidinic endonuclease 1 is required for the processing of miR-221/222 in regulating expression of the tumor suppressor PTEN. Analysis of a cohort of different cancers supports the relevance of our findings for tumor biology. We also show that apurinic/apyrimidinic endonuclease 1 participates in RNA-interactomes and protein-interactomes involved in cancer development, thus indicating an unsuspected post-transcriptional effect on cancer genes.en_US
dc.languageEN
dc.language.isoenen_US
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleMammalian APE1 controls miRNA processing and its interactome is linked to cancer RNA metabolismen_US
dc.typeJournal articleen_US
dc.creator.authorAntoniali, Giulia
dc.creator.authorSerra, Fabrizio
dc.creator.authorLirussi, Lisa
dc.creator.authorTanaka, Mikiei
dc.creator.authorD'Ambrosio, Chiara
dc.creator.authorZhang, Shiheng
dc.creator.authorRadovic, Slobodanka
dc.creator.authorDalla, Emiliano
dc.creator.authorCiani, Yari
dc.creator.authorScaloni, Andrea
dc.creator.authorLi, Mengxia
dc.creator.authorPiazza, Silvano
dc.creator.authorTell, Gianluca
cristin.unitcode185,53,82,10
cristin.unitnameAvdeling for klinisk molekylærbiologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1550674
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Nature Communications&rft.volume=8&rft.spage=&rft.date=2017
dc.identifier.jtitleNature Communications
dc.identifier.volume8
dc.identifier.doihttp://dx.doi.org/10.1038/s41467-017-00842-8
dc.identifier.urnURN:NBN:no-66566
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2041-1723
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/64028/1/s41467-017-00842-8.pdf
dc.type.versionPublishedVersion
cristin.articleid797


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