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The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals
The Tomato Hybrid Proline-rich Protein (THyPRP) gene was specifically expressed in the tomato (Solanum lycopersicum) flower abscission zone (FAZ), and its stable antisense silencing under the control of an abscission zone (AZ)-specific promoter, Tomato Abscission Polygalacturonase4, significantly in...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981600/ https://www.ncbi.nlm.nih.gov/pubmed/29872533 http://dx.doi.org/10.1038/s41438-018-0033-2 |
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author | Sundaresan, Srivignesh Philosoph-Hadas, Sonia Ma, Chao Jiang, Cai-Zhong Riov, Joseph Mugasimangalam, Raja Kochanek, Betina Salim, Shoshana Reid, Michael S. Meir, Shimon |
author_facet | Sundaresan, Srivignesh Philosoph-Hadas, Sonia Ma, Chao Jiang, Cai-Zhong Riov, Joseph Mugasimangalam, Raja Kochanek, Betina Salim, Shoshana Reid, Michael S. Meir, Shimon |
author_sort | Sundaresan, Srivignesh |
collection | PubMed |
description | The Tomato Hybrid Proline-rich Protein (THyPRP) gene was specifically expressed in the tomato (Solanum lycopersicum) flower abscission zone (FAZ), and its stable antisense silencing under the control of an abscission zone (AZ)-specific promoter, Tomato Abscission Polygalacturonase4, significantly inhibited tomato pedicel abscission following flower removal. For understanding the THyPRP role in regulating pedicel abscission, a transcriptomic analysis of the FAZ of THyPRP-silenced plants was performed, using a newly developed AZ-specific tomato microarray chip. Decreased expression of THyPRP in the silenced plants was already observed before abscission induction, resulting in FAZ-specific altered gene expression of transcription factors, epigenetic modifiers, post-translational regulators, and transporters. Our data demonstrate that the effect of THyPRP silencing on pedicel abscission was not mediated by its effect on auxin balance, but by decreased ethylene biosynthesis and response. Additionally, THyPRP silencing revealed new players, which were demonstrated for the first time to be involved in regulating pedicel abscission processes. These include: gibberellin perception, Ca(2+)-Calmodulin signaling, Serpins and Small Ubiquitin-related Modifier proteins involved in post-translational modifications, Synthaxin and SNARE-like proteins, which participate in exocytosis, a process necessary for cell separation. These changes, occurring in the silenced plants early after flower removal, inhibited and/or delayed the acquisition of the competence of the FAZ cells to respond to ethylene signaling. Our results suggest that THyPRP acts as a master regulator of flower abscission in tomato, predominantly by playing a role in the regulation of the FAZ cell competence to respond to ethylene signals. |
format | Online Article Text |
id | pubmed-5981600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59816002018-06-05 The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals Sundaresan, Srivignesh Philosoph-Hadas, Sonia Ma, Chao Jiang, Cai-Zhong Riov, Joseph Mugasimangalam, Raja Kochanek, Betina Salim, Shoshana Reid, Michael S. Meir, Shimon Hortic Res Article The Tomato Hybrid Proline-rich Protein (THyPRP) gene was specifically expressed in the tomato (Solanum lycopersicum) flower abscission zone (FAZ), and its stable antisense silencing under the control of an abscission zone (AZ)-specific promoter, Tomato Abscission Polygalacturonase4, significantly inhibited tomato pedicel abscission following flower removal. For understanding the THyPRP role in regulating pedicel abscission, a transcriptomic analysis of the FAZ of THyPRP-silenced plants was performed, using a newly developed AZ-specific tomato microarray chip. Decreased expression of THyPRP in the silenced plants was already observed before abscission induction, resulting in FAZ-specific altered gene expression of transcription factors, epigenetic modifiers, post-translational regulators, and transporters. Our data demonstrate that the effect of THyPRP silencing on pedicel abscission was not mediated by its effect on auxin balance, but by decreased ethylene biosynthesis and response. Additionally, THyPRP silencing revealed new players, which were demonstrated for the first time to be involved in regulating pedicel abscission processes. These include: gibberellin perception, Ca(2+)-Calmodulin signaling, Serpins and Small Ubiquitin-related Modifier proteins involved in post-translational modifications, Synthaxin and SNARE-like proteins, which participate in exocytosis, a process necessary for cell separation. These changes, occurring in the silenced plants early after flower removal, inhibited and/or delayed the acquisition of the competence of the FAZ cells to respond to ethylene signaling. Our results suggest that THyPRP acts as a master regulator of flower abscission in tomato, predominantly by playing a role in the regulation of the FAZ cell competence to respond to ethylene signals. Nature Publishing Group UK 2018-06-01 /pmc/articles/PMC5981600/ /pubmed/29872533 http://dx.doi.org/10.1038/s41438-018-0033-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sundaresan, Srivignesh Philosoph-Hadas, Sonia Ma, Chao Jiang, Cai-Zhong Riov, Joseph Mugasimangalam, Raja Kochanek, Betina Salim, Shoshana Reid, Michael S. Meir, Shimon The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals |
title | The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals |
title_full | The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals |
title_fullStr | The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals |
title_full_unstemmed | The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals |
title_short | The Tomato Hybrid Proline-rich Protein regulates the abscission zone competence to respond to ethylene signals |
title_sort | tomato hybrid proline-rich protein regulates the abscission zone competence to respond to ethylene signals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5981600/ https://www.ncbi.nlm.nih.gov/pubmed/29872533 http://dx.doi.org/10.1038/s41438-018-0033-2 |
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