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Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice

BACKGROUND: NCA1 (NO CATALASE ACTIVITY 1) was recently identified in Arabidopsis as a chaperone protein to regulate catalase (CAT) activity through maintaining the folding of CAT. The gene exists mainly in higher plants; some plants, such as Arabidopsis, contain only one NCA1 gene, whereas some othe...

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Autores principales: Liu, Jianzhe, Cui, Lili, Xie, Zongwang, Zhang, Zhisheng, Liu, Ee, Peng, Xinxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421683/
https://www.ncbi.nlm.nih.gov/pubmed/30885124
http://dx.doi.org/10.1186/s12870-019-1707-0
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author Liu, Jianzhe
Cui, Lili
Xie, Zongwang
Zhang, Zhisheng
Liu, Ee
Peng, Xinxiang
author_facet Liu, Jianzhe
Cui, Lili
Xie, Zongwang
Zhang, Zhisheng
Liu, Ee
Peng, Xinxiang
author_sort Liu, Jianzhe
collection PubMed
description BACKGROUND: NCA1 (NO CATALASE ACTIVITY 1) was recently identified in Arabidopsis as a chaperone protein to regulate catalase (CAT) activity through maintaining the folding of CAT. The gene exists mainly in higher plants; some plants, such as Arabidopsis, contain only one NCA1 gene, whereas some others such as rice harbor two copies. It is not yet understood whether and how both isoforms have functioned to regulate CAT activity in those two-copy-containing plant species. RESULTS: In this study, we first noticed that the spatiotemporal expression patterns of NCA1a and NCA1b were very similar in rice plants. Subsequent BiFC and yeast three-hybrid experiments demonstrated that both NCA1a and NCA1b show mutually exclusive, rather than simultaneous, interaction with CAT. For a further functional analysis, nca1a and nca1b single mutants or double mutants of rice were generated by CRISPR/Cas9. Analysis on these mutants under both normal and salinity stress conditions found that, as compared with WT, either nca1a or nca1b single mutant showed no difference at phenotypes and CAT activities, whereas the double mutants constantly displayed very low CAT activity (about 5%) and serious lesion phenotypes. CONCLUSIONS: These results suggest that NCA1a and NCA1b show mutually exclusive interaction with CAT to regulate CAT activity in a functionally-redundant manner in rice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1707-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-64216832019-03-28 Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice Liu, Jianzhe Cui, Lili Xie, Zongwang Zhang, Zhisheng Liu, Ee Peng, Xinxiang BMC Plant Biol Research Article BACKGROUND: NCA1 (NO CATALASE ACTIVITY 1) was recently identified in Arabidopsis as a chaperone protein to regulate catalase (CAT) activity through maintaining the folding of CAT. The gene exists mainly in higher plants; some plants, such as Arabidopsis, contain only one NCA1 gene, whereas some others such as rice harbor two copies. It is not yet understood whether and how both isoforms have functioned to regulate CAT activity in those two-copy-containing plant species. RESULTS: In this study, we first noticed that the spatiotemporal expression patterns of NCA1a and NCA1b were very similar in rice plants. Subsequent BiFC and yeast three-hybrid experiments demonstrated that both NCA1a and NCA1b show mutually exclusive, rather than simultaneous, interaction with CAT. For a further functional analysis, nca1a and nca1b single mutants or double mutants of rice were generated by CRISPR/Cas9. Analysis on these mutants under both normal and salinity stress conditions found that, as compared with WT, either nca1a or nca1b single mutant showed no difference at phenotypes and CAT activities, whereas the double mutants constantly displayed very low CAT activity (about 5%) and serious lesion phenotypes. CONCLUSIONS: These results suggest that NCA1a and NCA1b show mutually exclusive interaction with CAT to regulate CAT activity in a functionally-redundant manner in rice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1707-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-03-18 /pmc/articles/PMC6421683/ /pubmed/30885124 http://dx.doi.org/10.1186/s12870-019-1707-0 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
Liu, Jianzhe
Cui, Lili
Xie, Zongwang
Zhang, Zhisheng
Liu, Ee
Peng, Xinxiang
Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice
title Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice
title_full Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice
title_fullStr Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice
title_full_unstemmed Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice
title_short Two NCA1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice
title_sort two nca1 isoforms interact with catalase in a mutually exclusive manner to redundantly regulate its activity in rice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421683/
https://www.ncbi.nlm.nih.gov/pubmed/30885124
http://dx.doi.org/10.1186/s12870-019-1707-0
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