Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Zhihong, He, Yan, Li, Liangjian, Zhang, Xiaobo, Xu, Xia, Shi, Yongfeng, Wu, Jian-Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
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
_version_ 1783652245501378560
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
work_keys_str_mv AT zhangzhihong characterizationofanovelalleleencodingpheophorbideaoxygenaseinrice
AT heyan characterizationofanovelalleleencodingpheophorbideaoxygenaseinrice
AT liliangjian characterizationofanovelalleleencodingpheophorbideaoxygenaseinrice
AT zhangxiaobo characterizationofanovelalleleencodingpheophorbideaoxygenaseinrice
AT xuxia characterizationofanovelalleleencodingpheophorbideaoxygenaseinrice
AT shiyongfeng characterizationofanovelalleleencodingpheophorbideaoxygenaseinrice
AT wujianli characterizationofanovelalleleencodingpheophorbideaoxygenaseinrice