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CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance

BACKGROUND: NPR1, nonexpressor of pathogenesis-related gene 1, is a master regulator involved in plant defense response to pathogens, and its regulatory mechanism in the defense pathway has been relatively clear. However, information about the function of NPR1 in plant response to abiotic stress is...

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Autores principales: Li, Rui, Liu, Chunxue, Zhao, Ruirui, Wang, Liu, Chen, Lin, Yu, Wenqing, Zhang, Shujuan, Sheng, Jiping, Shen, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341727/
https://www.ncbi.nlm.nih.gov/pubmed/30669982
http://dx.doi.org/10.1186/s12870-018-1627-4
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author Li, Rui
Liu, Chunxue
Zhao, Ruirui
Wang, Liu
Chen, Lin
Yu, Wenqing
Zhang, Shujuan
Sheng, Jiping
Shen, Lin
author_facet Li, Rui
Liu, Chunxue
Zhao, Ruirui
Wang, Liu
Chen, Lin
Yu, Wenqing
Zhang, Shujuan
Sheng, Jiping
Shen, Lin
author_sort Li, Rui
collection PubMed
description BACKGROUND: NPR1, nonexpressor of pathogenesis-related gene 1, is a master regulator involved in plant defense response to pathogens, and its regulatory mechanism in the defense pathway has been relatively clear. However, information about the function of NPR1 in plant response to abiotic stress is still limited. Tomato is the fourth most economically crop worldwide and also one of the best-characterized model plants employed in genetic studies. Because of the lack of a stable tomato NPR1 (SlNPR1) mutant, little is known about the function of SlNPR1 in tomato response to biotic and abiotic stresses. RESULTS: Here we isolated SlNPR1 from tomato ‘Ailsa Craig’ and generated slnpr1 mutants using the CRISPR/Cas9 system. Analysis of the cis-acting elements indicated that SlNPR1 might be involved in tomato plant response to drought stress. Expression pattern analysis showed that SlNPR1 was expressed in all plant tissues, and it was strongly induced by drought stress. Thus, we investigated the function of SlNPR1 in tomato-plant drought tolerance. Results showed that slnpr1 mutants exhibited reduced drought tolerance with increased stomatal aperture, higher electrolytic leakage, malondialdehyde (MDA) and hydrogen peroxide (H(2)O(2)) levels, and lower activity levels of antioxidant enzymes, compared to wild type (WT) plants. The reduced drought tolerance of slnpr1 mutants was further reflected by the down-regulated expression of drought related key genes, including SlGST, SlDHN, and SlDREB. CONCLUSIONS: Collectively, the data suggest that SlNPR1 is involved in regulating tomato plant drought response. These results aid in further understanding the molecular basis underlying SlNPR1 mediation of tomato drought sensitivity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1627-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-63417272019-01-24 CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance Li, Rui Liu, Chunxue Zhao, Ruirui Wang, Liu Chen, Lin Yu, Wenqing Zhang, Shujuan Sheng, Jiping Shen, Lin BMC Plant Biol Research Article BACKGROUND: NPR1, nonexpressor of pathogenesis-related gene 1, is a master regulator involved in plant defense response to pathogens, and its regulatory mechanism in the defense pathway has been relatively clear. However, information about the function of NPR1 in plant response to abiotic stress is still limited. Tomato is the fourth most economically crop worldwide and also one of the best-characterized model plants employed in genetic studies. Because of the lack of a stable tomato NPR1 (SlNPR1) mutant, little is known about the function of SlNPR1 in tomato response to biotic and abiotic stresses. RESULTS: Here we isolated SlNPR1 from tomato ‘Ailsa Craig’ and generated slnpr1 mutants using the CRISPR/Cas9 system. Analysis of the cis-acting elements indicated that SlNPR1 might be involved in tomato plant response to drought stress. Expression pattern analysis showed that SlNPR1 was expressed in all plant tissues, and it was strongly induced by drought stress. Thus, we investigated the function of SlNPR1 in tomato-plant drought tolerance. Results showed that slnpr1 mutants exhibited reduced drought tolerance with increased stomatal aperture, higher electrolytic leakage, malondialdehyde (MDA) and hydrogen peroxide (H(2)O(2)) levels, and lower activity levels of antioxidant enzymes, compared to wild type (WT) plants. The reduced drought tolerance of slnpr1 mutants was further reflected by the down-regulated expression of drought related key genes, including SlGST, SlDHN, and SlDREB. CONCLUSIONS: Collectively, the data suggest that SlNPR1 is involved in regulating tomato plant drought response. These results aid in further understanding the molecular basis underlying SlNPR1 mediation of tomato drought sensitivity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1627-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-22 /pmc/articles/PMC6341727/ /pubmed/30669982 http://dx.doi.org/10.1186/s12870-018-1627-4 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
Li, Rui
Liu, Chunxue
Zhao, Ruirui
Wang, Liu
Chen, Lin
Yu, Wenqing
Zhang, Shujuan
Sheng, Jiping
Shen, Lin
CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance
title CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance
title_full CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance
title_fullStr CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance
title_full_unstemmed CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance
title_short CRISPR/Cas9-Mediated SlNPR1 mutagenesis reduces tomato plant drought tolerance
title_sort crispr/cas9-mediated slnpr1 mutagenesis reduces tomato plant drought tolerance
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341727/
https://www.ncbi.nlm.nih.gov/pubmed/30669982
http://dx.doi.org/10.1186/s12870-018-1627-4
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