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dc.contributor.authorMiyamoto, Keien
dc.contributor.authorSuzuki, Ken-ichi Ten
dc.contributor.authorSuzuki, Miyukien
dc.contributor.authorSakane, Yutoen
dc.contributor.authorSakuma, Tetsushien
dc.contributor.authorHerberg, Sarahen
dc.contributor.authorSimeone, Angelaen
dc.contributor.authorSimpson, Daviden
dc.contributor.authorJullien, Jeromeen
dc.contributor.authorYamamoto, Takashien
dc.contributor.authorGurdon, Johnen
dc.date.accessioned2015-11-04T16:38:48Z
dc.date.available2015-11-04T16:38:48Z
dc.date.issued2015-11-18en
dc.identifier.citationPLoS ONE 2015 10(11): e0142946. doi:10.1371/journal.pone.0142946en
dc.identifier.issn1932-6203
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/252517
dc.description.abstractRecent advances in genome editing using programmable nucleases have revolutionized gene targeting in various organisms. Successful gene knock-out has been shown in Xenopus, a widely-used model organism, although a system enabling less mosaic knock-out in founder embryos (F0) needs to be explored in order to judge phenotypes in the F0 generation. Here, we injected modified highly active transcription activator-like effector nuclease (TALEN) mRNA to oocytes at the germinal vesicle (GV) stage, followed by in vitro maturation and intracytoplasmic sperm injection, to achieve a full knock-out in F0 embryos. Unlike conventional injection methods to fertilized embryos, the injection of TALEN mRNA into GV oocytes allows expression of nucleases before fertilization, enabling them to work from an earlier stage. Using this procedure, most of developed embryos showed full knock-out phenotypes of the pigmentation gene tyrosinase and/or embryonic lethal gene pax6 in the founder generation. In addition, our method permitted a large 1 kb deletion. Thus, we describe nearly complete gene knock-out phenotypes in Xenopus laevis F0 embryos. The presented method will help to accelerate the production of knock-out frogs since we can bypass an extra generation of about 1 year in Xenopus laevis. Meantime, our method provides a unique opportunity to rapidly test the developmental effects of disrupting those genes that do not permit growth to an adult able to reproduce. In addition, the protocol shown here is considerably less invasive than the previously used host transfer since our protocol does not require surgery. The experimental scheme presented is potentially applicable to other organisms such as mammals and fish to resolve common issues of mosaicism in founders.
dc.description.sponsorshipK.M. was a Research Fellow at Wolfson College and was supported by the Herchel Smith Postdoctoral Fellowship.
dc.languageEnglishen
dc.language.isoenen
dc.publisherPLoS
dc.rightsCreative Commons Attribution 4.0 International License
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleThe expression of TALEN before fertilization provides a rapid knock-out phenotype in Xenopus laevis founder embryosen
dc.typeArticle
dc.description.versionThis is the final version of the article. It first appeared from PLOS via http://dx.doi.org/10.1371/journal.pone.0142946en
prism.numbere0142946en
prism.publicationDate2015en
prism.publicationNamePLoS ONEen
prism.volume10en
dcterms.dateAccepted2015-10-28en
rioxxterms.versionofrecord10.1371/journal.pone.0142946en
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserveden
rioxxterms.licenseref.startdate2015-11-18en
dc.contributor.orcidJullien, Jerome [0000-0002-7868-0021]
dc.contributor.orcidGurdon, John [0000-0002-5621-3799]
dc.identifier.eissn1932-6203
rioxxterms.typeJournal Article/Reviewen
pubs.funder-project-idWellcome Trust (101050/Z/13/Z)


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Creative Commons Attribution 4.0 International License
Except where otherwise noted, this item's licence is described as Creative Commons Attribution 4.0 International License