dc.contributor.author | Altae-Tran, Han | |
dc.contributor.author | Kannan, Soumya | |
dc.contributor.author | Demircioglu, F Esra | |
dc.contributor.author | Oshiro, Rachel | |
dc.contributor.author | Nety, Suchita P | |
dc.contributor.author | McKay, Luke J | |
dc.contributor.author | Dlakić, Mensur | |
dc.contributor.author | Inskeep, William P | |
dc.contributor.author | Makarova, Kira S | |
dc.contributor.author | Macrae, Rhiannon K | |
dc.contributor.author | Koonin, Eugene V | |
dc.contributor.author | Zhang, Feng | |
dc.date.accessioned | 2022-04-25T17:24:22Z | |
dc.date.available | 2022-04-25T17:24:22Z | |
dc.date.issued | 2021-10 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/142061 | |
dc.description.abstract | IscB proteins are putative nucleases encoded in a distinct family of IS200/IS605 transposons and are likely ancestors of the RNA-guided endonuclease Cas9, but the functions of IscB and its interactions with any RNA remain uncharacterized. Using evolutionary analysis, RNA sequencing, and biochemical experiments, we reconstructed the evolution of CRISPR-Cas9 systems from IS200/IS605 transposons. We found that IscB uses a single noncoding RNA for RNA-guided cleavage of double-stranded DNA and can be harnessed for genome editing in human cells. We also demonstrate the RNA-guided nuclease activity of TnpB, another IS200/IS605 transposon-encoded protein and the likely ancestor of Cas12 endonucleases. This work reveals a widespread class of transposon-encoded RNA-guided nucleases, which we name OMEGA (obligate mobile element–guided activity), with strong potential for developing as biotechnologies. | en_US |
dc.language.iso | en | |
dc.publisher | American Association for the Advancement of Science (AAAS) | en_US |
dc.relation.isversionof | 10.1126/science.abj6856 | en_US |
dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | en_US |
dc.source | PMC | en_US |
dc.title | The widespread IS200/IS605 transposon family encodes diverse programmable RNA-guided endonucleases | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Altae-Tran, Han, Kannan, Soumya, Demircioglu, F Esra, Oshiro, Rachel, Nety, Suchita P et al. 2021. "The widespread IS200/IS605 transposon family encodes diverse programmable RNA-guided endonucleases." Science, 374 (6563). | |
dc.contributor.department | Howard Hughes Medical Institute | |
dc.contributor.department | McGovern Institute for Brain Research at MIT | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | |
dc.relation.journal | Science | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2022-04-25T17:17:41Z | |
dspace.orderedauthors | Altae-Tran, H; Kannan, S; Demircioglu, FE; Oshiro, R; Nety, SP; McKay, LJ; Dlakić, M; Inskeep, WP; Makarova, KS; Macrae, RK; Koonin, EV; Zhang, F | en_US |
dspace.date.submission | 2022-04-25T17:17:43Z | |
mit.journal.volume | 374 | en_US |
mit.journal.issue | 6563 | en_US |
mit.license | PUBLISHER_POLICY | |
mit.metadata.status | Authority Work and Publication Information Needed | en_US |