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dc.contributor.authorPapathanasiou, Stamatis
dc.contributor.authorMarkoulaki, Styliani
dc.contributor.authorBlaine, Logan J
dc.contributor.authorLeibowitz, Mitchell L
dc.contributor.authorZhang, Cheng-Zhong
dc.contributor.authorJaenisch, Rudolf
dc.contributor.authorPellman, David
dc.date.accessioned2022-12-12T18:28:20Z
dc.date.available2022-12-12T18:28:20Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/1721.1/146846
dc.description.abstract<jats:title>Abstract</jats:title><jats:p>Karyotype alterations have emerged as on-target complications from CRISPR-Cas9 genome editing. However, the events that lead to these karyotypic changes in embryos after Cas9-treatment remain unknown. Here, using imaging and single-cell genome sequencing of 8-cell stage embryos, we track both spontaneous and Cas9-induced karyotype aberrations through the first three divisions of embryonic development. We observe the generation of abnormal structures of the nucleus that arise as a consequence of errors in mitosis, including micronuclei and chromosome bridges, and determine their contribution to common karyotype aberrations including whole chromosome loss that has been recently reported after editing in embryos. Together, these data demonstrate that Cas9-mediated germline genome editing can lead to unwanted on-target side effects, including major chromosome structural alterations that can be propagated over several divisions of embryonic development.</jats:p>en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/S41467-021-26097-Yen_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleWhole chromosome loss and genomic instability in mouse embryos after CRISPR-Cas9 genome editingen_US
dc.typeArticleen_US
dc.identifier.citationPapathanasiou, Stamatis, Markoulaki, Styliani, Blaine, Logan J, Leibowitz, Mitchell L, Zhang, Cheng-Zhong et al. 2021. "Whole chromosome loss and genomic instability in mouse embryos after CRISPR-Cas9 genome editing." Nature Communications, 12 (1).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-12-12T18:16:43Z
dspace.orderedauthorsPapathanasiou, S; Markoulaki, S; Blaine, LJ; Leibowitz, ML; Zhang, C-Z; Jaenisch, R; Pellman, Den_US
dspace.date.submission2022-12-12T18:16:52Z
mit.journal.volume12en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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