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Adenine base editors catalyze cytosine conversions in human cells

DC Field Value Language
dc.contributor.authorKim, Heon Seok-
dc.contributor.authorJeong, You Kyeong-
dc.contributor.authorHur, Junho K.-
dc.contributor.authorKim, Jin-Soo-
dc.contributor.authorBae, Sangsu-
dc.date.accessioned2021-01-31T03:08:30Z-
dc.date.available2021-01-31T03:08:30Z-
dc.date.created2020-04-27-
dc.date.created2020-04-27-
dc.date.issued2019-10-
dc.identifier.citationNature Biotechnology, Vol.37 No.10, pp.1145-1148-
dc.identifier.issn1087-0156-
dc.identifier.other97595-
dc.identifier.urihttps://hdl.handle.net/10371/171743-
dc.description.abstractAdenine base editors comprise an adenosine deaminase, evolved in vitro, and a Cas9 nickase. Here, we show that in addition to converting adenine to guanine, adenine base editors also convert cytosine to guanine or thymine in a narrow editing window (positions 5-7) and in a confined TC*N sequence context. Adenine base editor-induced cytosine substitutions occur independently of adenosine conversions with an efficiency of up to 11.2% and reduce the number of suitable targeting sites for high-specificity base editing.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleAdenine base editors catalyze cytosine conversions in human cells-
dc.typeArticle-
dc.contributor.AlternativeAuthor김진수-
dc.identifier.doi10.1038/s41587-019-0254-4-
dc.citation.journaltitleNature Biotechnology-
dc.identifier.wosid000493315800015-
dc.identifier.scopusid2-s2.0-85072942908-
dc.citation.endpage1148-
dc.citation.number10-
dc.citation.startpage1145-
dc.citation.volume37-
dc.identifier.sci000493315800015-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorKim, Jin-Soo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusGENOMIC DNA-
dc.subject.keywordPlusTARGET-
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  • College of Natural Sciences
  • Department of Chemistry
Research Area Biology and Biochemistry

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