Cargando…
Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence
Light regulates leaf senescence and light deprivation causes large-scale transcriptional reprogramming to dismantle cellular components and remobilize nutrients to sink organs, such as seeds and storage tissue. We recently reported that in Arabidopsis (Arabidopsis thaliana), Phytochrome-Interacting...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844404/ https://www.ncbi.nlm.nih.gov/pubmed/27135344 http://dx.doi.org/10.3390/plants4030644 |
_version_ | 1782428765529309184 |
---|---|
author | Piao, Weilan Kim, Eun-Young Han, Su-Hyun Sakuraba, Yasuhito Paek, Nam-Chon |
author_facet | Piao, Weilan Kim, Eun-Young Han, Su-Hyun Sakuraba, Yasuhito Paek, Nam-Chon |
author_sort | Piao, Weilan |
collection | PubMed |
description | Light regulates leaf senescence and light deprivation causes large-scale transcriptional reprogramming to dismantle cellular components and remobilize nutrients to sink organs, such as seeds and storage tissue. We recently reported that in Arabidopsis (Arabidopsis thaliana), Phytochrome-Interacting Factor4 (PIF4) and PIF5 promote dark-induced senescence and natural senescence by directly activating the expression of typical senescence-associated genes (SAGs), including ORESARA1 (ORE1) and ETHYLENE INSENSITIVE3 (EIN3). In contrast, phytochrome B (PhyB) inhibits leaf senescence by repressing PIF4 and PIF5 at the post-translational level. Although we found how red light signaling represses leaf senescence in Arabidopsis, it remains unknown whether PhyB and/or PhyA are involved in leaf senescence in rice (Oryza sativa). Here we show that rice phyB knockout mutants (osphyB-1, -2, and -3) exhibited an early senescence phenotype during dark-induced senescence, but an osphyA knockout mutant (osphyA-3) senesced normally. The RT-qPCR analysis revealed that several senescence-associated genes, including OsORE1 and OsEIN3, were significantly up-regulated in osphyB-2 mutants, indicating that OsPhyB also inhibits leaf senescence, like Arabidopsis PhyB. We also found that leaf segments of osphyB-2 senesced faster even under light conditions. Supplementation with nitrogen compounds, such as KNO(3) and NH(4)NO(3), rescued the early senescence phenotype of osphyB-2, indicating that starvation is one of the major signaling factors in the OsPhyB-dependent leaf senescence pathway. |
format | Online Article Text |
id | pubmed-4844404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-48444042016-04-29 Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence Piao, Weilan Kim, Eun-Young Han, Su-Hyun Sakuraba, Yasuhito Paek, Nam-Chon Plants (Basel) Article Light regulates leaf senescence and light deprivation causes large-scale transcriptional reprogramming to dismantle cellular components and remobilize nutrients to sink organs, such as seeds and storage tissue. We recently reported that in Arabidopsis (Arabidopsis thaliana), Phytochrome-Interacting Factor4 (PIF4) and PIF5 promote dark-induced senescence and natural senescence by directly activating the expression of typical senescence-associated genes (SAGs), including ORESARA1 (ORE1) and ETHYLENE INSENSITIVE3 (EIN3). In contrast, phytochrome B (PhyB) inhibits leaf senescence by repressing PIF4 and PIF5 at the post-translational level. Although we found how red light signaling represses leaf senescence in Arabidopsis, it remains unknown whether PhyB and/or PhyA are involved in leaf senescence in rice (Oryza sativa). Here we show that rice phyB knockout mutants (osphyB-1, -2, and -3) exhibited an early senescence phenotype during dark-induced senescence, but an osphyA knockout mutant (osphyA-3) senesced normally. The RT-qPCR analysis revealed that several senescence-associated genes, including OsORE1 and OsEIN3, were significantly up-regulated in osphyB-2 mutants, indicating that OsPhyB also inhibits leaf senescence, like Arabidopsis PhyB. We also found that leaf segments of osphyB-2 senesced faster even under light conditions. Supplementation with nitrogen compounds, such as KNO(3) and NH(4)NO(3), rescued the early senescence phenotype of osphyB-2, indicating that starvation is one of the major signaling factors in the OsPhyB-dependent leaf senescence pathway. MDPI 2015-09-01 /pmc/articles/PMC4844404/ /pubmed/27135344 http://dx.doi.org/10.3390/plants4030644 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Piao, Weilan Kim, Eun-Young Han, Su-Hyun Sakuraba, Yasuhito Paek, Nam-Chon Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence |
title | Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence |
title_full | Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence |
title_fullStr | Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence |
title_full_unstemmed | Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence |
title_short | Rice Phytochrome B (OsPhyB) Negatively Regulates Dark- and Starvation-Induced Leaf Senescence |
title_sort | rice phytochrome b (osphyb) negatively regulates dark- and starvation-induced leaf senescence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844404/ https://www.ncbi.nlm.nih.gov/pubmed/27135344 http://dx.doi.org/10.3390/plants4030644 |
work_keys_str_mv | AT piaoweilan ricephytochromebosphybnegativelyregulatesdarkandstarvationinducedleafsenescence AT kimeunyoung ricephytochromebosphybnegativelyregulatesdarkandstarvationinducedleafsenescence AT hansuhyun ricephytochromebosphybnegativelyregulatesdarkandstarvationinducedleafsenescence AT sakurabayasuhito ricephytochromebosphybnegativelyregulatesdarkandstarvationinducedleafsenescence AT paeknamchon ricephytochromebosphybnegativelyregulatesdarkandstarvationinducedleafsenescence |