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Crystal Structure of Staphylococcus aureus Cas9

Authors :
Institute for Medical Engineering and Science
Massachusetts Institute of Technology. Department of Biological Engineering
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
McGovern Institute for Brain Research at MIT
Cong, Le
Yan, Winston Xia
Zetsche, Bernd
Li, Yinqing
Zhang, Feng
Nishimasu, Hiroshi
Ran, F. Ann
Kurabayashi, Arisa
Ishitani, Ryuichiro
Nureki, Osamu
Institute for Medical Engineering and Science
Massachusetts Institute of Technology. Department of Biological Engineering
Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
McGovern Institute for Brain Research at MIT
Cong, Le
Yan, Winston Xia
Zetsche, Bernd
Li, Yinqing
Zhang, Feng
Nishimasu, Hiroshi
Ran, F. Ann
Kurabayashi, Arisa
Ishitani, Ryuichiro
Nureki, Osamu
Source :
PMC
Publication Year :
2017

Abstract

Summary The RNA-guided DNA endonuclease Cas9 cleaves double-stranded DNA targets with a protospacer adjacent mot if (PAM) and complementarity to the guide RNA. Recently, we harnessed Staphylococcus aureus Cas9 (SaCas9), which is significantly smaller than Streptococcus pyogenes Cas9 (SpCas9), to facilitate efficient in vivo genome editing. Here, we report the crystal structures of SaCas9 in complex with a single guide RNA (sgRNA) and its double-stranded DNA targets, containing the 5′-TTGAAT-3′ PAM and the 5′-TTGGGT-3′ PAM, at 2.6 and 2.7 Å resolutions, respectively. The structures revealed the mechanism of the relaxed recognition of the 5′-NNGRRT-3′ PAM by SaCas9. A structural comparison of SaCas9 with SpCas9 highlighted both structural conservation and divergence, explaining their distinct PAM specificities and orthologous sgRNA recognition. Finally, we applied the structural information about this minimal Cas9 to rationally design compact transcriptional activators and inducible nucleases, to further expand the CRISPR-Cas9 genome editing toolbox.<br />National Institute of General Medical Sciences (U.S.) (Grant T32GM007753)<br />National Institutes of Health (U.S.) (Award 1DP1-MH100706)

Details

Database :
OAIster
Journal :
PMC
Notes :
application/pdf
Publication Type :
Electronic Resource
Accession number :
edsoai.on1141885850
Document Type :
Electronic Resource