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PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato

Plants experience low ambient temperature and low red to far-red ratios (L-R/FR) of light due to vegetative shading and longer twilight durations in cool seasons. Low temperature induce photoinhibition through inactivation of the photosynthetic apparatus, however, the role of light quality on photop...

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Autores principales: Wang, Feng, Yan, Jiarong, Ahammed, Golam Jalal, Wang, Xiujie, Bu, Xin, Xiang, Hengzuo, Li, Yanbing, Lu, Jiazhi, Liu, Yufeng, Qi, Hongyan, Qi, Mingfang, Li, Tianlai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270563/
https://www.ncbi.nlm.nih.gov/pubmed/32547581
http://dx.doi.org/10.3389/fpls.2020.00669
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author Wang, Feng
Yan, Jiarong
Ahammed, Golam Jalal
Wang, Xiujie
Bu, Xin
Xiang, Hengzuo
Li, Yanbing
Lu, Jiazhi
Liu, Yufeng
Qi, Hongyan
Qi, Mingfang
Li, Tianlai
author_facet Wang, Feng
Yan, Jiarong
Ahammed, Golam Jalal
Wang, Xiujie
Bu, Xin
Xiang, Hengzuo
Li, Yanbing
Lu, Jiazhi
Liu, Yufeng
Qi, Hongyan
Qi, Mingfang
Li, Tianlai
author_sort Wang, Feng
collection PubMed
description Plants experience low ambient temperature and low red to far-red ratios (L-R/FR) of light due to vegetative shading and longer twilight durations in cool seasons. Low temperature induce photoinhibition through inactivation of the photosynthetic apparatus, however, the role of light quality on photoprotection during cold stress remains poorly understood. Here, we report that L-R/FR significantly prevents the overreduction of the entire intersystem electron transfer chain and the limitation of photosystem I (PSI) acceptor side, eventually alleviating the cold-induced photoinhibition. During cold stress, L-R/FR activated cyclic electron flow (CEF), enhanced protonation of PSII subunit S (PsbS) and de-epoxidation state of the xanthophyll cycle, and promoted energy-dependent quenching (qE) component of non-photochemical quenching (NPQ), enzyme activity of Foyer-Halliwell-Asada cycle and D1 proteins accumulation. However, L-R/FR –induced photoprotection pathways were compromised in tomato PROTON GRADIENT REGULATION5 (PGR5) and PGR5-LIKE PHOTOSYNTHETIC PHENOTYPE1A (PGRL1A) co-silenced plants and NADH DEHYDROGENASE-LIKE COMPLEX M (NDHM) -silenced plants during cold stress. Our results demonstrate that both PGR5/PGRL1- and NDH-dependent CEF mediate L-R/FR –induced cold tolerance by enhancing the thermal dissipation and the repair of photodamaged PSII, thereby mitigating the overreduction of electron carriers and the accumulation of reactive oxygen species. The study indicates that there is an anterograde link between photoreception and photoprotection in tomato plants during cold stress.
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spelling pubmed-72705632020-06-15 PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato Wang, Feng Yan, Jiarong Ahammed, Golam Jalal Wang, Xiujie Bu, Xin Xiang, Hengzuo Li, Yanbing Lu, Jiazhi Liu, Yufeng Qi, Hongyan Qi, Mingfang Li, Tianlai Front Plant Sci Plant Science Plants experience low ambient temperature and low red to far-red ratios (L-R/FR) of light due to vegetative shading and longer twilight durations in cool seasons. Low temperature induce photoinhibition through inactivation of the photosynthetic apparatus, however, the role of light quality on photoprotection during cold stress remains poorly understood. Here, we report that L-R/FR significantly prevents the overreduction of the entire intersystem electron transfer chain and the limitation of photosystem I (PSI) acceptor side, eventually alleviating the cold-induced photoinhibition. During cold stress, L-R/FR activated cyclic electron flow (CEF), enhanced protonation of PSII subunit S (PsbS) and de-epoxidation state of the xanthophyll cycle, and promoted energy-dependent quenching (qE) component of non-photochemical quenching (NPQ), enzyme activity of Foyer-Halliwell-Asada cycle and D1 proteins accumulation. However, L-R/FR –induced photoprotection pathways were compromised in tomato PROTON GRADIENT REGULATION5 (PGR5) and PGR5-LIKE PHOTOSYNTHETIC PHENOTYPE1A (PGRL1A) co-silenced plants and NADH DEHYDROGENASE-LIKE COMPLEX M (NDHM) -silenced plants during cold stress. Our results demonstrate that both PGR5/PGRL1- and NDH-dependent CEF mediate L-R/FR –induced cold tolerance by enhancing the thermal dissipation and the repair of photodamaged PSII, thereby mitigating the overreduction of electron carriers and the accumulation of reactive oxygen species. The study indicates that there is an anterograde link between photoreception and photoprotection in tomato plants during cold stress. Frontiers Media S.A. 2020-05-27 /pmc/articles/PMC7270563/ /pubmed/32547581 http://dx.doi.org/10.3389/fpls.2020.00669 Text en Copyright © 2020 Wang, Yan, Ahammed, Wang, Bu, Xiang, Li, Lu, Liu, Qi, Qi and Li. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Wang, Feng
Yan, Jiarong
Ahammed, Golam Jalal
Wang, Xiujie
Bu, Xin
Xiang, Hengzuo
Li, Yanbing
Lu, Jiazhi
Liu, Yufeng
Qi, Hongyan
Qi, Mingfang
Li, Tianlai
PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato
title PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato
title_full PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato
title_fullStr PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato
title_full_unstemmed PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato
title_short PGR5/PGRL1 and NDH Mediate Far-Red Light-Induced Photoprotection in Response to Chilling Stress in Tomato
title_sort pgr5/pgrl1 and ndh mediate far-red light-induced photoprotection in response to chilling stress in tomato
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270563/
https://www.ncbi.nlm.nih.gov/pubmed/32547581
http://dx.doi.org/10.3389/fpls.2020.00669
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