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H and HL synergistically regulate jasmonate-triggered trichome formation in tomato
The development of trichomes, which protect plants against herbivores, is affected by various stresses. In tomato, previous studies showed that stress-triggered jasmonic acid (JA) signaling influences trichome formation, but the underlying mechanism is not fully resolved. Here, we found that two C2H...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973001/ https://www.ncbi.nlm.nih.gov/pubmed/35048113 http://dx.doi.org/10.1093/hr/uhab080 |
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author | Hua, Bing Chang, Jiang Han, Xiaoqian Xu, Zhijing Hu, Shourong Li, Shuang Wang, Renyin Yang, Liling Yang, Meina Wu, Shasha Shen, Jingyuan Yu, Xiaomin Wu, Shuang |
author_facet | Hua, Bing Chang, Jiang Han, Xiaoqian Xu, Zhijing Hu, Shourong Li, Shuang Wang, Renyin Yang, Liling Yang, Meina Wu, Shasha Shen, Jingyuan Yu, Xiaomin Wu, Shuang |
author_sort | Hua, Bing |
collection | PubMed |
description | The development of trichomes, which protect plants against herbivores, is affected by various stresses. In tomato, previous studies showed that stress-triggered jasmonic acid (JA) signaling influences trichome formation, but the underlying mechanism is not fully resolved. Here, we found that two C2H2 zinc finger proteins synergistically regulate JA-induced trichome formation in tomato. The naturally occurring mutations in the H gene and its close homolog H-like in a spontaneous mutant, LA3172, cause severely affected trichome development. Compared with the respective single mutant, the h/hl double mutant displayed more severe trichome defects in all tissues. Despite their partially redundant function, the H and HL genes regulate trichome formation in a spatially distinct manner, with HL more involved in hypocotyls and leaves while H is more involved in stems and sepals. Furthermore, the activity of H/HL is essential for JA-triggered trichome formation. The JA signaling inhibitor SlJAZ2 represses the activity of H and HL via physical interaction, resulting in the activation of THM1, a negative regulator of trichome formation. Our results provide novel insight into the mechanism of trichome formation in response to stress-induced JA signaling in tomato. |
format | Online Article Text |
id | pubmed-8973001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89730012022-04-04 H and HL synergistically regulate jasmonate-triggered trichome formation in tomato Hua, Bing Chang, Jiang Han, Xiaoqian Xu, Zhijing Hu, Shourong Li, Shuang Wang, Renyin Yang, Liling Yang, Meina Wu, Shasha Shen, Jingyuan Yu, Xiaomin Wu, Shuang Hortic Res Article The development of trichomes, which protect plants against herbivores, is affected by various stresses. In tomato, previous studies showed that stress-triggered jasmonic acid (JA) signaling influences trichome formation, but the underlying mechanism is not fully resolved. Here, we found that two C2H2 zinc finger proteins synergistically regulate JA-induced trichome formation in tomato. The naturally occurring mutations in the H gene and its close homolog H-like in a spontaneous mutant, LA3172, cause severely affected trichome development. Compared with the respective single mutant, the h/hl double mutant displayed more severe trichome defects in all tissues. Despite their partially redundant function, the H and HL genes regulate trichome formation in a spatially distinct manner, with HL more involved in hypocotyls and leaves while H is more involved in stems and sepals. Furthermore, the activity of H/HL is essential for JA-triggered trichome formation. The JA signaling inhibitor SlJAZ2 represses the activity of H and HL via physical interaction, resulting in the activation of THM1, a negative regulator of trichome formation. Our results provide novel insight into the mechanism of trichome formation in response to stress-induced JA signaling in tomato. Oxford University Press 2022-01-20 /pmc/articles/PMC8973001/ /pubmed/35048113 http://dx.doi.org/10.1093/hr/uhab080 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nanjing Agricultural University https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Hua, Bing Chang, Jiang Han, Xiaoqian Xu, Zhijing Hu, Shourong Li, Shuang Wang, Renyin Yang, Liling Yang, Meina Wu, Shasha Shen, Jingyuan Yu, Xiaomin Wu, Shuang H and HL synergistically regulate jasmonate-triggered trichome formation in tomato |
title | H and HL synergistically regulate jasmonate-triggered trichome formation in tomato |
title_full | H and HL synergistically regulate jasmonate-triggered trichome formation in tomato |
title_fullStr | H and HL synergistically regulate jasmonate-triggered trichome formation in tomato |
title_full_unstemmed | H and HL synergistically regulate jasmonate-triggered trichome formation in tomato |
title_short | H and HL synergistically regulate jasmonate-triggered trichome formation in tomato |
title_sort | h and hl synergistically regulate jasmonate-triggered trichome formation in tomato |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8973001/ https://www.ncbi.nlm.nih.gov/pubmed/35048113 http://dx.doi.org/10.1093/hr/uhab080 |
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