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HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth
Light plays an important role in determining plant architecture, which greatly influences crop yield. However, the precise mechanisms by which light signaling regulates bud outgrowth remain to be identified. Here, we show that light regulates bud outgrowth via both HY5 and brassinosteroid (BR)-depen...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120035/ https://www.ncbi.nlm.nih.gov/pubmed/37036969 http://dx.doi.org/10.1073/pnas.2301879120 |
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author | Dong, Han Wang, Jiachun Song, Xuewei Hu, Chaoyi Zhu, Changan Sun, Ting Zhou, Zhiwen Hu, Zhangjian Xia, Xiaojian Zhou, Jie Shi, Kai Zhou, Yanhong Foyer, Christine H. Yu, Jingquan |
author_facet | Dong, Han Wang, Jiachun Song, Xuewei Hu, Chaoyi Zhu, Changan Sun, Ting Zhou, Zhiwen Hu, Zhangjian Xia, Xiaojian Zhou, Jie Shi, Kai Zhou, Yanhong Foyer, Christine H. Yu, Jingquan |
author_sort | Dong, Han |
collection | PubMed |
description | Light plays an important role in determining plant architecture, which greatly influences crop yield. However, the precise mechanisms by which light signaling regulates bud outgrowth remain to be identified. Here, we show that light regulates bud outgrowth via both HY5 and brassinosteroid (BR)-dependent pathways in tomato. Inactivation of the red-light photoreceptor PHYB, or deficiencies in PHYB or the blue-light photoreceptor CRY1a, inhibits bud outgrowth and leads to decreased accumulation of HY5 protein and increased transcript level of BRANCHED1 (BRC1), a central integrator of branching signals. HY5, functioning as a mobile systemic signal from leaves, promotes bud outgrowth by directly suppressing BRC1 transcript and activating the transcript of BR biosynthesis genes within the lateral buds in tomato. Furthermore, BRC1 prevents the accumulation of cytokinin (CK) and gibberellin (GA) by directly inhibiting the transcript of CK synthesis gene LOG4, while increasing the transcript levels of CK and GA degradation genes (CKX7, GA2ox4, and GA2ox5), leading to an arrest of bud outgrowth. Moreover, bud outgrowth occurs predominantly in the day due to the suppression of BRC1 transcript by HY5. These findings demonstrate that light-inducible HY5 acts as a systemic signaling factor in fine-tuning the bud outgrowth of tomato. |
format | Online Article Text |
id | pubmed-10120035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-101200352023-04-22 HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth Dong, Han Wang, Jiachun Song, Xuewei Hu, Chaoyi Zhu, Changan Sun, Ting Zhou, Zhiwen Hu, Zhangjian Xia, Xiaojian Zhou, Jie Shi, Kai Zhou, Yanhong Foyer, Christine H. Yu, Jingquan Proc Natl Acad Sci U S A Biological Sciences Light plays an important role in determining plant architecture, which greatly influences crop yield. However, the precise mechanisms by which light signaling regulates bud outgrowth remain to be identified. Here, we show that light regulates bud outgrowth via both HY5 and brassinosteroid (BR)-dependent pathways in tomato. Inactivation of the red-light photoreceptor PHYB, or deficiencies in PHYB or the blue-light photoreceptor CRY1a, inhibits bud outgrowth and leads to decreased accumulation of HY5 protein and increased transcript level of BRANCHED1 (BRC1), a central integrator of branching signals. HY5, functioning as a mobile systemic signal from leaves, promotes bud outgrowth by directly suppressing BRC1 transcript and activating the transcript of BR biosynthesis genes within the lateral buds in tomato. Furthermore, BRC1 prevents the accumulation of cytokinin (CK) and gibberellin (GA) by directly inhibiting the transcript of CK synthesis gene LOG4, while increasing the transcript levels of CK and GA degradation genes (CKX7, GA2ox4, and GA2ox5), leading to an arrest of bud outgrowth. Moreover, bud outgrowth occurs predominantly in the day due to the suppression of BRC1 transcript by HY5. These findings demonstrate that light-inducible HY5 acts as a systemic signaling factor in fine-tuning the bud outgrowth of tomato. National Academy of Sciences 2023-04-10 2023-04-18 /pmc/articles/PMC10120035/ /pubmed/37036969 http://dx.doi.org/10.1073/pnas.2301879120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Dong, Han Wang, Jiachun Song, Xuewei Hu, Chaoyi Zhu, Changan Sun, Ting Zhou, Zhiwen Hu, Zhangjian Xia, Xiaojian Zhou, Jie Shi, Kai Zhou, Yanhong Foyer, Christine H. Yu, Jingquan HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth |
title | HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth |
title_full | HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth |
title_fullStr | HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth |
title_full_unstemmed | HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth |
title_short | HY5 functions as a systemic signal by integrating BRC1-dependent hormone signaling in tomato bud outgrowth |
title_sort | hy5 functions as a systemic signal by integrating brc1-dependent hormone signaling in tomato bud outgrowth |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120035/ https://www.ncbi.nlm.nih.gov/pubmed/37036969 http://dx.doi.org/10.1073/pnas.2301879120 |
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