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dc.date.accessioned2024-02-20T17:59:47Z
dc.date.available2024-02-20T17:59:47Z
dc.date.created2024-01-29T12:19:30Z
dc.date.issued2024
dc.identifier.citationLópez-Porras, Adrián Berg, Ragnhild Stenberg Burgerhout, Erik Hansen, Øyvind J Györkei, Ádám Qiao, Shuo-Wang Johansen, Finn-Eirik . CRISPR-Cas9/Cas12a-based genome editing in Atlantic cod (Gadus morhua). Aquaculture. 2024, 581, 1-9
dc.identifier.urihttp://hdl.handle.net/10852/108348
dc.description.abstractAquaculture is the fastest-growing food sector worldwide but faces sustainability challenges that need to be addressed in many ways, including genetic enhancement. Atlantic cod has re-emerged as an aquaculture species and tools for genetic manipulation are needed. Thus, we compared five formats of CRISPR to determine which was most efficient to generate knock outs in Atlantic cod. Cas9 protein was presented in preformed ribonucleoprotein (RNP) complexes with single guide or with duplex guide RNAs or an mRNA encoding Cas9 was used with the same two formats of guide RNAs. Cas12a was tested as RNP complexes with single guide RNAs. We found Cas9 mRNA with single guide RNA to be the most efficient format to knock out both alleles of the slc45a2 gene, which resulted in an albino-like phenotype in up to 75% of surviving larvae. DNA analysis of individual larvae revealed mosaic genotypes with variable indel mutations. The mortality of injected eggs was high, resulting in low overall efficiency. Nevertheless, this study lays the foundation for further genetic and functional research using the CRISPR/Cas9 genome editing system in Atlantic cod.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleCRISPR-Cas9/Cas12a-based genome editing in Atlantic cod (Gadus morhua)
dc.title.alternativeENEngelskEnglishCRISPR-Cas9/Cas12a-based genome editing in Atlantic cod (Gadus morhua)
dc.typeJournal article
dc.creator.authorLópez-Porras, Adrián
dc.creator.authorBerg, Ragnhild Stenberg
dc.creator.authorBurgerhout, Erik
dc.creator.authorHansen, Øyvind J
dc.creator.authorGyörkei, Ádám
dc.creator.authorQiao, Shuo-Wang
dc.creator.authorJohansen, Finn-Eirik
cristin.unitcode185,15,29,30
cristin.unitnameSeksjon for fysiologi og cellebiologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2236823
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Aquaculture&rft.volume=581&rft.spage=1&rft.date=2024
dc.identifier.jtitleAquaculture
dc.identifier.volume581
dc.identifier.doihttps://doi.org/10.1016/j.aquaculture.2023.740440
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0044-8486
dc.type.versionPublishedVersion
cristin.articleid740440
dc.relation.projectNOFIMA/12946
dc.relation.projectNOFIMA/13284
dc.relation.projectNFR/301965


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