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MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems
Efficient generation of plants carrying mutations in multiple genes remains a challenge. Using two or more orthogonal CRISPR/Cas systems can generate plants with multi-gene mutations, but assembly of these systems requires a robust, high-capacity toolkit. Here, we describe MISSA 2.0 (multiple-round...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290471/ https://www.ncbi.nlm.nih.gov/pubmed/28155921 http://dx.doi.org/10.1038/srep41993 |
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author | Zhang, Hai-Yan Wang, Xing-Hui Dong, Li Wang, Zhi-Ping Liu, Bing Lv, Jie Xing, Hui-Li Han, Chun-Yan Wang, Xue-Chen Chen, Qi-Jun |
author_facet | Zhang, Hai-Yan Wang, Xing-Hui Dong, Li Wang, Zhi-Ping Liu, Bing Lv, Jie Xing, Hui-Li Han, Chun-Yan Wang, Xue-Chen Chen, Qi-Jun |
author_sort | Zhang, Hai-Yan |
collection | PubMed |
description | Efficient generation of plants carrying mutations in multiple genes remains a challenge. Using two or more orthogonal CRISPR/Cas systems can generate plants with multi-gene mutations, but assembly of these systems requires a robust, high-capacity toolkit. Here, we describe MISSA 2.0 (multiple-round in vivo site-specific assembly 2.0), an extensively updated toolkit for assembly of two or more CRISPR/Cas systems. We developed a novel suicide donor vector system based on plasmid RK2, which has much higher cloning capacity than the original, plasmid R6K-based system. We validated the utility of MISSA 2.0 by assembling multiple DNA fragments into the E. coli chromosome, and by creating transgenic Arabidopsis thaliana that constitutively or inducibly overexpress multiple genes. We then demonstrated that the higher cloning capacity of the RK2-derived MISSA 2.0 donor vectors facilitated the assembly of two orthogonal CRISPR/Cas systems including SpCas9 and SaCas9, and thus facilitated the creation of transgenic lines harboring these systems. We anticipate that MISSA 2.0 will enable substantial advancements in multiplex genome editing based on two or more orthogonal CRISPR/Cas9 systems, as well as in plant synthetic biology. |
format | Online Article Text |
id | pubmed-5290471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52904712017-02-06 MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems Zhang, Hai-Yan Wang, Xing-Hui Dong, Li Wang, Zhi-Ping Liu, Bing Lv, Jie Xing, Hui-Li Han, Chun-Yan Wang, Xue-Chen Chen, Qi-Jun Sci Rep Article Efficient generation of plants carrying mutations in multiple genes remains a challenge. Using two or more orthogonal CRISPR/Cas systems can generate plants with multi-gene mutations, but assembly of these systems requires a robust, high-capacity toolkit. Here, we describe MISSA 2.0 (multiple-round in vivo site-specific assembly 2.0), an extensively updated toolkit for assembly of two or more CRISPR/Cas systems. We developed a novel suicide donor vector system based on plasmid RK2, which has much higher cloning capacity than the original, plasmid R6K-based system. We validated the utility of MISSA 2.0 by assembling multiple DNA fragments into the E. coli chromosome, and by creating transgenic Arabidopsis thaliana that constitutively or inducibly overexpress multiple genes. We then demonstrated that the higher cloning capacity of the RK2-derived MISSA 2.0 donor vectors facilitated the assembly of two orthogonal CRISPR/Cas systems including SpCas9 and SaCas9, and thus facilitated the creation of transgenic lines harboring these systems. We anticipate that MISSA 2.0 will enable substantial advancements in multiplex genome editing based on two or more orthogonal CRISPR/Cas9 systems, as well as in plant synthetic biology. Nature Publishing Group 2017-02-03 /pmc/articles/PMC5290471/ /pubmed/28155921 http://dx.doi.org/10.1038/srep41993 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhang, Hai-Yan Wang, Xing-Hui Dong, Li Wang, Zhi-Ping Liu, Bing Lv, Jie Xing, Hui-Li Han, Chun-Yan Wang, Xue-Chen Chen, Qi-Jun MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems |
title | MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems |
title_full | MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems |
title_fullStr | MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems |
title_full_unstemmed | MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems |
title_short | MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems |
title_sort | missa 2.0: an updated synthetic biology toolbox for assembly of orthogonal crispr/cas systems |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5290471/ https://www.ncbi.nlm.nih.gov/pubmed/28155921 http://dx.doi.org/10.1038/srep41993 |
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