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Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis

BACKGROUND: CRISPR-Cas12a (formerly Cpf1) is an RNA-guided endonuclease with distinct features that have expanded genome editing capabilities. Cas12a-mediated genome editing is temperature sensitive in plants, but a lack of a comprehensive understanding on Cas12a temperature sensitivity in plant cel...

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Autores principales: Malzahn, Aimee A., Tang, Xu, Lee, Keunsub, Ren, Qiurong, Sretenovic, Simon, Zhang, Yingxiao, Chen, Hongqiao, Kang, Minjeong, Bao, Yu, Zheng, Xuelian, Deng, Kejun, Zhang, Tao, Salcedo, Valeria, Wang, Kan, Zhang, Yong, Qi, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357469/
https://www.ncbi.nlm.nih.gov/pubmed/30704461
http://dx.doi.org/10.1186/s12915-019-0629-5
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author Malzahn, Aimee A.
Tang, Xu
Lee, Keunsub
Ren, Qiurong
Sretenovic, Simon
Zhang, Yingxiao
Chen, Hongqiao
Kang, Minjeong
Bao, Yu
Zheng, Xuelian
Deng, Kejun
Zhang, Tao
Salcedo, Valeria
Wang, Kan
Zhang, Yong
Qi, Yiping
author_facet Malzahn, Aimee A.
Tang, Xu
Lee, Keunsub
Ren, Qiurong
Sretenovic, Simon
Zhang, Yingxiao
Chen, Hongqiao
Kang, Minjeong
Bao, Yu
Zheng, Xuelian
Deng, Kejun
Zhang, Tao
Salcedo, Valeria
Wang, Kan
Zhang, Yong
Qi, Yiping
author_sort Malzahn, Aimee A.
collection PubMed
description BACKGROUND: CRISPR-Cas12a (formerly Cpf1) is an RNA-guided endonuclease with distinct features that have expanded genome editing capabilities. Cas12a-mediated genome editing is temperature sensitive in plants, but a lack of a comprehensive understanding on Cas12a temperature sensitivity in plant cells has hampered effective application of Cas12a nucleases in plant genome editing. RESULTS: We compared AsCas12a, FnCas12a, and LbCas12a for their editing efficiencies and non-homologous end joining (NHEJ) repair profiles at four different temperatures in rice. We found that AsCas12a is more sensitive to temperature and that it requires a temperature of over 28 °C for high activity. Each Cas12a nuclease exhibited distinct indel mutation profiles which were not affected by temperatures. For the first time, we successfully applied AsCas12a for generating rice mutants with high frequencies up to 93% among T0 lines. We next pursued editing in the dicot model plant Arabidopsis, for which Cas12a-based genome editing has not been previously demonstrated. While LbCas12a barely showed any editing activity at 22 °C, its editing activity was rescued by growing the transgenic plants at 29 °C. With an early high-temperature treatment regime, we successfully achieved germline editing at the two target genes, GL2 and TT4, in Arabidopsis transgenic lines. We then used high-temperature treatment to improve Cas12a-mediated genome editing in maize. By growing LbCas12a T0 maize lines at 28 °C, we obtained Cas12a-edited mutants at frequencies up to 100% in the T1 generation. Finally, we demonstrated DNA binding of Cas12a was not abolished at lower temperatures by using a dCas12a-SRDX-based transcriptional repression system in Arabidopsis. CONCLUSION: Our study demonstrates the use of high-temperature regimes to achieve high editing efficiencies with Cas12a systems in rice, Arabidopsis, and maize and sheds light on the mechanism of temperature sensitivity for Cas12a in plants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0629-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-63574692019-02-07 Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis Malzahn, Aimee A. Tang, Xu Lee, Keunsub Ren, Qiurong Sretenovic, Simon Zhang, Yingxiao Chen, Hongqiao Kang, Minjeong Bao, Yu Zheng, Xuelian Deng, Kejun Zhang, Tao Salcedo, Valeria Wang, Kan Zhang, Yong Qi, Yiping BMC Biol Research Article BACKGROUND: CRISPR-Cas12a (formerly Cpf1) is an RNA-guided endonuclease with distinct features that have expanded genome editing capabilities. Cas12a-mediated genome editing is temperature sensitive in plants, but a lack of a comprehensive understanding on Cas12a temperature sensitivity in plant cells has hampered effective application of Cas12a nucleases in plant genome editing. RESULTS: We compared AsCas12a, FnCas12a, and LbCas12a for their editing efficiencies and non-homologous end joining (NHEJ) repair profiles at four different temperatures in rice. We found that AsCas12a is more sensitive to temperature and that it requires a temperature of over 28 °C for high activity. Each Cas12a nuclease exhibited distinct indel mutation profiles which were not affected by temperatures. For the first time, we successfully applied AsCas12a for generating rice mutants with high frequencies up to 93% among T0 lines. We next pursued editing in the dicot model plant Arabidopsis, for which Cas12a-based genome editing has not been previously demonstrated. While LbCas12a barely showed any editing activity at 22 °C, its editing activity was rescued by growing the transgenic plants at 29 °C. With an early high-temperature treatment regime, we successfully achieved germline editing at the two target genes, GL2 and TT4, in Arabidopsis transgenic lines. We then used high-temperature treatment to improve Cas12a-mediated genome editing in maize. By growing LbCas12a T0 maize lines at 28 °C, we obtained Cas12a-edited mutants at frequencies up to 100% in the T1 generation. Finally, we demonstrated DNA binding of Cas12a was not abolished at lower temperatures by using a dCas12a-SRDX-based transcriptional repression system in Arabidopsis. CONCLUSION: Our study demonstrates the use of high-temperature regimes to achieve high editing efficiencies with Cas12a systems in rice, Arabidopsis, and maize and sheds light on the mechanism of temperature sensitivity for Cas12a in plants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0629-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-31 /pmc/articles/PMC6357469/ /pubmed/30704461 http://dx.doi.org/10.1186/s12915-019-0629-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Malzahn, Aimee A.
Tang, Xu
Lee, Keunsub
Ren, Qiurong
Sretenovic, Simon
Zhang, Yingxiao
Chen, Hongqiao
Kang, Minjeong
Bao, Yu
Zheng, Xuelian
Deng, Kejun
Zhang, Tao
Salcedo, Valeria
Wang, Kan
Zhang, Yong
Qi, Yiping
Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis
title Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis
title_full Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis
title_fullStr Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis
title_full_unstemmed Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis
title_short Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis
title_sort application of crispr-cas12a temperature sensitivity for improved genome editing in rice, maize, and arabidopsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357469/
https://www.ncbi.nlm.nih.gov/pubmed/30704461
http://dx.doi.org/10.1186/s12915-019-0629-5
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