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Characterization of a novel allele encoding pheophorbide a oxygenase in rice
We identified a rapid cell death 2 (rcd2) mutant from an indica cultivar Zhongjian100 mutant bank. The red-brown lesions appeared firstly on young seedling leaves, then gradually merged and the leaves completely withered at the late tillering stage. rcd2 displayed apparent cell death at/around the l...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889113/ https://www.ncbi.nlm.nih.gov/pubmed/33369525 http://dx.doi.org/10.1080/15592324.2020.1864606 |
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author | Zhang, Zhihong He, Yan Li, Liangjian Zhang, Xiaobo Xu, Xia Shi, Yongfeng Wu, Jian-Li |
author_facet | Zhang, Zhihong He, Yan Li, Liangjian Zhang, Xiaobo Xu, Xia Shi, Yongfeng Wu, Jian-Li |
author_sort | Zhang, Zhihong |
collection | PubMed |
description | We identified a rapid cell death 2 (rcd2) mutant from an indica cultivar Zhongjian100 mutant bank. The red-brown lesions appeared firstly on young seedling leaves, then gradually merged and the leaves completely withered at the late tillering stage. rcd2 displayed apparent cell death at/around the lesions, accumulation of superoxide anion (O(2)(−)) and disturbed ROS scavenging system, impaired photosynthetic capacity with significantly reduced chlorophyll content. The lesion formation was controlled by a single recessive nuclear gene and induced by natural light as well as mechanical wounding. A single base mutation (A1726T) at the 6th exon of OsMH_03G0040800 resulted in I576F substitution in the encoding protein, pheophorbide a oxygenase (PAO). Functional complementation could rescue the mutant phenotype and PAO-knockout lines exhibited the similar phenotype to rcd2. The activity of PAO decreased significantly while the content of PAO substrate, pheophorbide a, increased apparently in rcd2. The expression of chlorophyll synthesis/degradation-related genes and the contents of metabolic intermediates were largely changed. Furthermore, the level of chlorophyllide a, the product of chlorophyllase, increased significantly, indicating chlorophyllase might play a role in chlorophyll degradation in rice. Our results suggested that the I576F substitution disrupted PAO function, leading to O(2)(−) accumulation and chlorophyll degradation breakdown in rice. |
format | Online Article Text |
id | pubmed-7889113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-78891132021-02-23 Characterization of a novel allele encoding pheophorbide a oxygenase in rice Zhang, Zhihong He, Yan Li, Liangjian Zhang, Xiaobo Xu, Xia Shi, Yongfeng Wu, Jian-Li Plant Signal Behav Research Paper We identified a rapid cell death 2 (rcd2) mutant from an indica cultivar Zhongjian100 mutant bank. The red-brown lesions appeared firstly on young seedling leaves, then gradually merged and the leaves completely withered at the late tillering stage. rcd2 displayed apparent cell death at/around the lesions, accumulation of superoxide anion (O(2)(−)) and disturbed ROS scavenging system, impaired photosynthetic capacity with significantly reduced chlorophyll content. The lesion formation was controlled by a single recessive nuclear gene and induced by natural light as well as mechanical wounding. A single base mutation (A1726T) at the 6th exon of OsMH_03G0040800 resulted in I576F substitution in the encoding protein, pheophorbide a oxygenase (PAO). Functional complementation could rescue the mutant phenotype and PAO-knockout lines exhibited the similar phenotype to rcd2. The activity of PAO decreased significantly while the content of PAO substrate, pheophorbide a, increased apparently in rcd2. The expression of chlorophyll synthesis/degradation-related genes and the contents of metabolic intermediates were largely changed. Furthermore, the level of chlorophyllide a, the product of chlorophyllase, increased significantly, indicating chlorophyllase might play a role in chlorophyll degradation in rice. Our results suggested that the I576F substitution disrupted PAO function, leading to O(2)(−) accumulation and chlorophyll degradation breakdown in rice. Taylor & Francis 2020-12-28 /pmc/articles/PMC7889113/ /pubmed/33369525 http://dx.doi.org/10.1080/15592324.2020.1864606 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Paper Zhang, Zhihong He, Yan Li, Liangjian Zhang, Xiaobo Xu, Xia Shi, Yongfeng Wu, Jian-Li Characterization of a novel allele encoding pheophorbide a oxygenase in rice |
title | Characterization of a novel allele encoding pheophorbide a oxygenase in rice |
title_full | Characterization of a novel allele encoding pheophorbide a oxygenase in rice |
title_fullStr | Characterization of a novel allele encoding pheophorbide a oxygenase in rice |
title_full_unstemmed | Characterization of a novel allele encoding pheophorbide a oxygenase in rice |
title_short | Characterization of a novel allele encoding pheophorbide a oxygenase in rice |
title_sort | characterization of a novel allele encoding pheophorbide a oxygenase in rice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889113/ https://www.ncbi.nlm.nih.gov/pubmed/33369525 http://dx.doi.org/10.1080/15592324.2020.1864606 |
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