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Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation
Staphylococcus aureus Cas9 (SaCas9) is an RNA‐guided endonuclease that targets complementary DNA adjacent to a protospacer adjacent motif (PAM) for cleavage. Its small size facilitates in vivo delivery for genome editing in various organisms. Herein, using single‐molecule and ensemble approaches, we...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534634/ https://www.ncbi.nlm.nih.gov/pubmed/32790142 http://dx.doi.org/10.15252/embr.202050184 |
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author | Zhang, Siqi Zhang, Qian Hou, Xi‐Miao Guo, Lijuan Wang, Fangzhu Bi, Lulu Zhang, Xia Li, Hai‐Hong Wen, Fengcai Xi, Xu‐Guang Huang, Xingxu Shen, Bin Sun, Bo |
author_facet | Zhang, Siqi Zhang, Qian Hou, Xi‐Miao Guo, Lijuan Wang, Fangzhu Bi, Lulu Zhang, Xia Li, Hai‐Hong Wen, Fengcai Xi, Xu‐Guang Huang, Xingxu Shen, Bin Sun, Bo |
author_sort | Zhang, Siqi |
collection | PubMed |
description | Staphylococcus aureus Cas9 (SaCas9) is an RNA‐guided endonuclease that targets complementary DNA adjacent to a protospacer adjacent motif (PAM) for cleavage. Its small size facilitates in vivo delivery for genome editing in various organisms. Herein, using single‐molecule and ensemble approaches, we systemically study the mechanism of SaCas9 underlying its interplay with DNA. We find that the DNA binding and cleavage of SaCas9 require complementarities of 6‐ and 18‐bp of PAM‐proximal DNA with guide RNA, respectively. These activities are mediated by two steady interactions among the ternary complex, one of which is located approximately 6 bp from the PAM and beyond the apparent footprint of SaCas9 on DNA. Notably, the other interaction within the protospacer is significantly strong and thus poses DNA‐bound SaCas9 a persistent block to DNA‐tracking motors. Intriguingly, after cleavage, SaCas9 autonomously releases the PAM‐distal DNA while retaining binding to the PAM. This partial DNA release immediately abolishes its strong interaction with the protospacer DNA and consequently promotes its subsequent dissociation from the PAM. Overall, these data provide a dynamic understanding of SaCas9 and instruct its effective applications. |
format | Online Article Text |
id | pubmed-7534634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75346342020-10-07 Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation Zhang, Siqi Zhang, Qian Hou, Xi‐Miao Guo, Lijuan Wang, Fangzhu Bi, Lulu Zhang, Xia Li, Hai‐Hong Wen, Fengcai Xi, Xu‐Guang Huang, Xingxu Shen, Bin Sun, Bo EMBO Rep Articles Staphylococcus aureus Cas9 (SaCas9) is an RNA‐guided endonuclease that targets complementary DNA adjacent to a protospacer adjacent motif (PAM) for cleavage. Its small size facilitates in vivo delivery for genome editing in various organisms. Herein, using single‐molecule and ensemble approaches, we systemically study the mechanism of SaCas9 underlying its interplay with DNA. We find that the DNA binding and cleavage of SaCas9 require complementarities of 6‐ and 18‐bp of PAM‐proximal DNA with guide RNA, respectively. These activities are mediated by two steady interactions among the ternary complex, one of which is located approximately 6 bp from the PAM and beyond the apparent footprint of SaCas9 on DNA. Notably, the other interaction within the protospacer is significantly strong and thus poses DNA‐bound SaCas9 a persistent block to DNA‐tracking motors. Intriguingly, after cleavage, SaCas9 autonomously releases the PAM‐distal DNA while retaining binding to the PAM. This partial DNA release immediately abolishes its strong interaction with the protospacer DNA and consequently promotes its subsequent dissociation from the PAM. Overall, these data provide a dynamic understanding of SaCas9 and instruct its effective applications. John Wiley and Sons Inc. 2020-08-13 2020-10-05 /pmc/articles/PMC7534634/ /pubmed/32790142 http://dx.doi.org/10.15252/embr.202050184 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Zhang, Siqi Zhang, Qian Hou, Xi‐Miao Guo, Lijuan Wang, Fangzhu Bi, Lulu Zhang, Xia Li, Hai‐Hong Wen, Fengcai Xi, Xu‐Guang Huang, Xingxu Shen, Bin Sun, Bo Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation |
title | Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation |
title_full | Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation |
title_fullStr | Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation |
title_full_unstemmed | Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation |
title_short | Dynamics of Staphylococcus aureus Cas9 in DNA target Association and Dissociation |
title_sort | dynamics of staphylococcus aureus cas9 in dna target association and dissociation |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534634/ https://www.ncbi.nlm.nih.gov/pubmed/32790142 http://dx.doi.org/10.15252/embr.202050184 |
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