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Direct observation of DNA target searching and cleavage by CRISPR-Cas12a
Cas12a (also called Cpf1) is a representative type V-A CRISPR effector RNA-guided DNA endonuclease, which provides an alternative to type II CRISPR–Cas9 for genome editing. Previous studies have revealed that Cas12a has unique features distinct from Cas9, but the detailed mechanisms of target search...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050341/ https://www.ncbi.nlm.nih.gov/pubmed/30018371 http://dx.doi.org/10.1038/s41467-018-05245-x |
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author | Jeon, Yongmoon Choi, You Hee Jang, Yunsu Yu, Jihyeon Goo, Jiyoung Lee, Gyejun Jeong, You Kyeong Lee, Seung Hwan Kim, In-San Kim, Jin-Soo Jeong, Cherlhyun Lee, Sanghwa Bae, Sangsu |
author_facet | Jeon, Yongmoon Choi, You Hee Jang, Yunsu Yu, Jihyeon Goo, Jiyoung Lee, Gyejun Jeong, You Kyeong Lee, Seung Hwan Kim, In-San Kim, Jin-Soo Jeong, Cherlhyun Lee, Sanghwa Bae, Sangsu |
author_sort | Jeon, Yongmoon |
collection | PubMed |
description | Cas12a (also called Cpf1) is a representative type V-A CRISPR effector RNA-guided DNA endonuclease, which provides an alternative to type II CRISPR–Cas9 for genome editing. Previous studies have revealed that Cas12a has unique features distinct from Cas9, but the detailed mechanisms of target searching and DNA cleavage by Cas12a are still unclear. Here, we directly observe this entire process by using single-molecule fluorescence assays to study Cas12a from Acidaminococcus sp. (AsCas12a). We determine that AsCas12a ribonucleoproteins search for their on-target site by a one-dimensional diffusion along elongated DNA molecules and induce cleavage in the two DNA strands in a well-defined order, beginning with the non-target strand. Furthermore, the protospacer-adjacent motif (PAM) for AsCas12a makes only a limited contribution of DNA unwinding during R-loop formation and shows a negligible role in the process of DNA cleavage, in contrast to the Cas9 PAM. |
format | Online Article Text |
id | pubmed-6050341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60503412018-07-23 Direct observation of DNA target searching and cleavage by CRISPR-Cas12a Jeon, Yongmoon Choi, You Hee Jang, Yunsu Yu, Jihyeon Goo, Jiyoung Lee, Gyejun Jeong, You Kyeong Lee, Seung Hwan Kim, In-San Kim, Jin-Soo Jeong, Cherlhyun Lee, Sanghwa Bae, Sangsu Nat Commun Article Cas12a (also called Cpf1) is a representative type V-A CRISPR effector RNA-guided DNA endonuclease, which provides an alternative to type II CRISPR–Cas9 for genome editing. Previous studies have revealed that Cas12a has unique features distinct from Cas9, but the detailed mechanisms of target searching and DNA cleavage by Cas12a are still unclear. Here, we directly observe this entire process by using single-molecule fluorescence assays to study Cas12a from Acidaminococcus sp. (AsCas12a). We determine that AsCas12a ribonucleoproteins search for their on-target site by a one-dimensional diffusion along elongated DNA molecules and induce cleavage in the two DNA strands in a well-defined order, beginning with the non-target strand. Furthermore, the protospacer-adjacent motif (PAM) for AsCas12a makes only a limited contribution of DNA unwinding during R-loop formation and shows a negligible role in the process of DNA cleavage, in contrast to the Cas9 PAM. Nature Publishing Group UK 2018-07-17 /pmc/articles/PMC6050341/ /pubmed/30018371 http://dx.doi.org/10.1038/s41467-018-05245-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jeon, Yongmoon Choi, You Hee Jang, Yunsu Yu, Jihyeon Goo, Jiyoung Lee, Gyejun Jeong, You Kyeong Lee, Seung Hwan Kim, In-San Kim, Jin-Soo Jeong, Cherlhyun Lee, Sanghwa Bae, Sangsu Direct observation of DNA target searching and cleavage by CRISPR-Cas12a |
title | Direct observation of DNA target searching and cleavage by CRISPR-Cas12a |
title_full | Direct observation of DNA target searching and cleavage by CRISPR-Cas12a |
title_fullStr | Direct observation of DNA target searching and cleavage by CRISPR-Cas12a |
title_full_unstemmed | Direct observation of DNA target searching and cleavage by CRISPR-Cas12a |
title_short | Direct observation of DNA target searching and cleavage by CRISPR-Cas12a |
title_sort | direct observation of dna target searching and cleavage by crispr-cas12a |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050341/ https://www.ncbi.nlm.nih.gov/pubmed/30018371 http://dx.doi.org/10.1038/s41467-018-05245-x |
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