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dc.contributor.authorKato, Kazuki
dc.contributor.authorOkazaki, Sae
dc.contributor.authorKannan, Soumya
dc.contributor.authorAltae-Tran, Han
dc.contributor.authorEsra Demircioglu, F
dc.contributor.authorIsayama, Yukari
dc.contributor.authorIshikawa, Junichiro
dc.contributor.authorFukuda, Masahiro
dc.contributor.authorMacrae, Rhiannon K
dc.contributor.authorNishizawa, Tomohiro
dc.contributor.authorMakarova, Kira S
dc.contributor.authorKoonin, Eugene V
dc.contributor.authorZhang, Feng
dc.contributor.authorNishimasu, Hiroshi
dc.date.accessioned2023-04-03T19:48:57Z
dc.date.available2023-04-03T19:48:57Z
dc.date.issued2022-11-07
dc.identifier.urihttps://hdl.handle.net/1721.1/150366
dc.description.abstract<jats:title>Abstract</jats:title><jats:p>Transposon-encoded IscB family proteins are RNA-guided nucleases in the OMEGA (obligate mobile element-guided activity) system, and likely ancestors of the RNA-guided nuclease Cas9 in the type II CRISPR-Cas adaptive immune system. IscB associates with its cognate ωRNA to form a ribonucleoprotein complex that cleaves double-stranded DNA targets complementary to an ωRNA guide segment. Although IscB shares the RuvC and HNH endonuclease domains with Cas9, it is much smaller than Cas9, mainly due to the lack of the α-helical nucleic-acid recognition lobe. Here, we report the cryo-electron microscopy structure of an IscB protein from the human gut metagenome (OgeuIscB) in complex with its cognate ωRNA and a target DNA, at 2.6-Å resolution. This high-resolution structure reveals the detailed architecture of the IscB–ωRNA ribonucleoprotein complex, and shows how the small IscB protein assembles with the ωRNA and mediates RNA-guided DNA cleavage. The large ωRNA scaffold structurally and functionally compensates for the recognition lobe of Cas9, and participates in the recognition of the guide RNA–target DNA heteroduplex. These findings provide insights into the mechanism of the programmable DNA cleavage by the IscB–ωRNA complex and the evolution of the type II CRISPR-Cas9 effector complexes.</jats:p>en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/s41467-022-34378-3en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Communicationsen_US
dc.titleStructure of the IscB–ωRNA ribonucleoprotein complex, the likely ancestor of CRISPR-Cas9en_US
dc.typeArticleen_US
dc.identifier.citationKato, Kazuki, Okazaki, Sae, Kannan, Soumya, Altae-Tran, Han, Esra Demircioglu, F et al. 2022. "Structure of the IscB–ωRNA ribonucleoprotein complex, the likely ancestor of CRISPR-Cas9." Nature Communications, 13 (1).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_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.updated2023-04-03T19:45:56Z
dspace.orderedauthorsKato, K; Okazaki, S; Kannan, S; Altae-Tran, H; Esra Demircioglu, F; Isayama, Y; Ishikawa, J; Fukuda, M; Macrae, RK; Nishizawa, T; Makarova, KS; Koonin, EV; Zhang, F; Nishimasu, Hen_US
dspace.date.submission2023-04-03T19:45:59Z
mit.journal.volume13en_US
mit.journal.issue1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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