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SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato

Facultative parthenocarpy is of great practical value. However, the molecular mechanism underlying facultative parthenocarpy remains elusive. Transcriptional co-repressors (TPL) act as a central regulatory hub controlling all nine phytohormone pathways. Previously, we proved that SlTPLs participate...

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Autores principales: He, Mi, Song, Shiwei, Zhu, Xiaoyang, Lin, Yuxiang, Pan, Zanlin, Chen, Lin, Chen, Da, Hu, Guojian, Huang, Baowen, Chen, Mengyi, Wu, Caiyu, Chen, Riyuan, Bouzayen, Mondher, Zouine, Mohammed, Hao, Yanwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174789/
https://www.ncbi.nlm.nih.gov/pubmed/34093628
http://dx.doi.org/10.3389/fpls.2021.672232
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author He, Mi
Song, Shiwei
Zhu, Xiaoyang
Lin, Yuxiang
Pan, Zanlin
Chen, Lin
Chen, Da
Hu, Guojian
Huang, Baowen
Chen, Mengyi
Wu, Caiyu
Chen, Riyuan
Bouzayen, Mondher
Zouine, Mohammed
Hao, Yanwei
author_facet He, Mi
Song, Shiwei
Zhu, Xiaoyang
Lin, Yuxiang
Pan, Zanlin
Chen, Lin
Chen, Da
Hu, Guojian
Huang, Baowen
Chen, Mengyi
Wu, Caiyu
Chen, Riyuan
Bouzayen, Mondher
Zouine, Mohammed
Hao, Yanwei
author_sort He, Mi
collection PubMed
description Facultative parthenocarpy is of great practical value. However, the molecular mechanism underlying facultative parthenocarpy remains elusive. Transcriptional co-repressors (TPL) act as a central regulatory hub controlling all nine phytohormone pathways. Previously, we proved that SlTPLs participate in the auxin signaling pathway by interacting with auxin/indole acetic acid (Aux/IAAs) in tomato; however, their function in fruit development has not been studied. In addition to their high expression levels during flower development, the interaction between SlTPL1 and SlIAA9 stimulated the investigation of its functional significance via RNA interference (RNAi) technology, whereby the translation of a protein is prevented by selective degradation of its encoded mRNA. Down-regulation of SlTPL1 resulted in facultative parthenocarpy. Plants of SlTPL1-RNAi transgenic lines produced similar fruits which did not show any pleiotropic effects under normal conditions. However, they produced seedless fruits upon emasculation and under heat stress conditions. Furthermore, SlTPL1-RNAi flower buds contained higher levels of cytokinins and lower levels of abscisic acid. To reveal how SlTPL1 regulates facultative parthenocarpy, RNA-seq was performed to identify genes regulated by SlTPL1 in ovaries before and after fruit set. The results showed that down-regulation of SlTPL1 resulted in reduced expression levels of cytokinin metabolism-related genes, and all transcription factors such as MYB, CDF, and ERFs. Conversely, down-regulation of SlTPL1 induced the expression of genes related to cell wall and cytoskeleton organization. These data provide novel insights into the molecular mechanism of facultative tomato parthenocarpy and identify SlTPL1 as a key factor regulating these processes.
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spelling pubmed-81747892021-06-04 SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato He, Mi Song, Shiwei Zhu, Xiaoyang Lin, Yuxiang Pan, Zanlin Chen, Lin Chen, Da Hu, Guojian Huang, Baowen Chen, Mengyi Wu, Caiyu Chen, Riyuan Bouzayen, Mondher Zouine, Mohammed Hao, Yanwei Front Plant Sci Plant Science Facultative parthenocarpy is of great practical value. However, the molecular mechanism underlying facultative parthenocarpy remains elusive. Transcriptional co-repressors (TPL) act as a central regulatory hub controlling all nine phytohormone pathways. Previously, we proved that SlTPLs participate in the auxin signaling pathway by interacting with auxin/indole acetic acid (Aux/IAAs) in tomato; however, their function in fruit development has not been studied. In addition to their high expression levels during flower development, the interaction between SlTPL1 and SlIAA9 stimulated the investigation of its functional significance via RNA interference (RNAi) technology, whereby the translation of a protein is prevented by selective degradation of its encoded mRNA. Down-regulation of SlTPL1 resulted in facultative parthenocarpy. Plants of SlTPL1-RNAi transgenic lines produced similar fruits which did not show any pleiotropic effects under normal conditions. However, they produced seedless fruits upon emasculation and under heat stress conditions. Furthermore, SlTPL1-RNAi flower buds contained higher levels of cytokinins and lower levels of abscisic acid. To reveal how SlTPL1 regulates facultative parthenocarpy, RNA-seq was performed to identify genes regulated by SlTPL1 in ovaries before and after fruit set. The results showed that down-regulation of SlTPL1 resulted in reduced expression levels of cytokinin metabolism-related genes, and all transcription factors such as MYB, CDF, and ERFs. Conversely, down-regulation of SlTPL1 induced the expression of genes related to cell wall and cytoskeleton organization. These data provide novel insights into the molecular mechanism of facultative tomato parthenocarpy and identify SlTPL1 as a key factor regulating these processes. Frontiers Media S.A. 2021-05-20 /pmc/articles/PMC8174789/ /pubmed/34093628 http://dx.doi.org/10.3389/fpls.2021.672232 Text en Copyright © 2021 He, Song, Zhu, Lin, Pan, Chen, Chen, Hu, Huang, Chen, Wu, Chen, Bouzayen, Zouine and Hao. https://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
He, Mi
Song, Shiwei
Zhu, Xiaoyang
Lin, Yuxiang
Pan, Zanlin
Chen, Lin
Chen, Da
Hu, Guojian
Huang, Baowen
Chen, Mengyi
Wu, Caiyu
Chen, Riyuan
Bouzayen, Mondher
Zouine, Mohammed
Hao, Yanwei
SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato
title SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato
title_full SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato
title_fullStr SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato
title_full_unstemmed SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato
title_short SlTPL1 Silencing Induces Facultative Parthenocarpy in Tomato
title_sort sltpl1 silencing induces facultative parthenocarpy in tomato
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8174789/
https://www.ncbi.nlm.nih.gov/pubmed/34093628
http://dx.doi.org/10.3389/fpls.2021.672232
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