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PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1

Bud dormancy, which enables damage from cold temperatures to be avoided during winter and early spring, is an important adaptive mechanism of deciduous fruit trees to cope with seasonal environmental changes and temperate climates. Understanding the regulatory mechanism of bud break in fruit trees i...

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Autores principales: Zhang, Yuzheng, Tan, Qiuping, Wang, Ning, Meng, Xiangguang, He, Huajie, Wen, Binbin, Xiao, Wei, Chen, Xiude, Li, Dongmei, Fu, Xiling, Li, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413399/
https://www.ncbi.nlm.nih.gov/pubmed/36035719
http://dx.doi.org/10.3389/fpls.2022.971482
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author Zhang, Yuzheng
Tan, Qiuping
Wang, Ning
Meng, Xiangguang
He, Huajie
Wen, Binbin
Xiao, Wei
Chen, Xiude
Li, Dongmei
Fu, Xiling
Li, Ling
author_facet Zhang, Yuzheng
Tan, Qiuping
Wang, Ning
Meng, Xiangguang
He, Huajie
Wen, Binbin
Xiao, Wei
Chen, Xiude
Li, Dongmei
Fu, Xiling
Li, Ling
author_sort Zhang, Yuzheng
collection PubMed
description Bud dormancy, which enables damage from cold temperatures to be avoided during winter and early spring, is an important adaptive mechanism of deciduous fruit trees to cope with seasonal environmental changes and temperate climates. Understanding the regulatory mechanism of bud break in fruit trees is highly important for the artificial control of bud break and the prevention of spring frost damage. However, the molecular mechanism underlying the involvement of MYB TFs during the bud break of peach is still unclear. In this study, we isolated and identified the PpMYB52 (Prupe.5G240000.1) gene from peach; this gene is downregulated in the process of bud break, upregulated in response to ABA and downregulated in response to GA. Overexpression of PpMYB52 suppresses the germination of transgenic tomato seeds. In addition, Y2H, Bimolecular fluorescence complementation (BiFC) assays verified that PpMYB52 interacts with a RING-type E3 ubiquitin ligase, PpMIEL1, which is upregulated during bud break may positively regulate peach bud break by ubiquitination-mediated degradation of PpMYB52. Our findings are the first to characterize the molecular mechanisms underlying the involvement of MYB TFs in peach bud break, increasing awareness of dormancy-related molecules to avoid bud damage in perennial deciduous fruit trees.
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spelling pubmed-94133992022-08-27 PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1 Zhang, Yuzheng Tan, Qiuping Wang, Ning Meng, Xiangguang He, Huajie Wen, Binbin Xiao, Wei Chen, Xiude Li, Dongmei Fu, Xiling Li, Ling Front Plant Sci Plant Science Bud dormancy, which enables damage from cold temperatures to be avoided during winter and early spring, is an important adaptive mechanism of deciduous fruit trees to cope with seasonal environmental changes and temperate climates. Understanding the regulatory mechanism of bud break in fruit trees is highly important for the artificial control of bud break and the prevention of spring frost damage. However, the molecular mechanism underlying the involvement of MYB TFs during the bud break of peach is still unclear. In this study, we isolated and identified the PpMYB52 (Prupe.5G240000.1) gene from peach; this gene is downregulated in the process of bud break, upregulated in response to ABA and downregulated in response to GA. Overexpression of PpMYB52 suppresses the germination of transgenic tomato seeds. In addition, Y2H, Bimolecular fluorescence complementation (BiFC) assays verified that PpMYB52 interacts with a RING-type E3 ubiquitin ligase, PpMIEL1, which is upregulated during bud break may positively regulate peach bud break by ubiquitination-mediated degradation of PpMYB52. Our findings are the first to characterize the molecular mechanisms underlying the involvement of MYB TFs in peach bud break, increasing awareness of dormancy-related molecules to avoid bud damage in perennial deciduous fruit trees. Frontiers Media S.A. 2022-08-10 /pmc/articles/PMC9413399/ /pubmed/36035719 http://dx.doi.org/10.3389/fpls.2022.971482 Text en Copyright © 2022 Zhang, Tan, Wang, Meng, He, Wen, Xiao, Chen, Li, Fu and Li. 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
Zhang, Yuzheng
Tan, Qiuping
Wang, Ning
Meng, Xiangguang
He, Huajie
Wen, Binbin
Xiao, Wei
Chen, Xiude
Li, Dongmei
Fu, Xiling
Li, Ling
PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1
title PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1
title_full PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1
title_fullStr PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1
title_full_unstemmed PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1
title_short PpMYB52 negatively regulates peach bud break through the gibberellin pathway and through interactions with PpMIEL1
title_sort ppmyb52 negatively regulates peach bud break through the gibberellin pathway and through interactions with ppmiel1
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413399/
https://www.ncbi.nlm.nih.gov/pubmed/36035719
http://dx.doi.org/10.3389/fpls.2022.971482
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