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NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development
The transcription factor Woolly (Wo) and its downstream gene CycB2 have been shown to regulate trichome development in tomato (Solanum lycopersicum). It has been demonstrated that only the gain-of-function allele of Slwo (SlWo(V), the Slwo woolly motif mutant allele) can increase the trichome densit...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242068/ https://www.ncbi.nlm.nih.gov/pubmed/31990970 http://dx.doi.org/10.1093/jxb/erz542 |
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author | Wu, Min-Liang Cui, Yu-Chao Ge, Li Cui, Li-Peng Xu, Zhi-Chao Zhang, Hong-Ying Wang, Zhao-Jun Zhou, Dan Wu, Shuang Chen, Liang Cui, Hong |
author_facet | Wu, Min-Liang Cui, Yu-Chao Ge, Li Cui, Li-Peng Xu, Zhi-Chao Zhang, Hong-Ying Wang, Zhao-Jun Zhou, Dan Wu, Shuang Chen, Liang Cui, Hong |
author_sort | Wu, Min-Liang |
collection | PubMed |
description | The transcription factor Woolly (Wo) and its downstream gene CycB2 have been shown to regulate trichome development in tomato (Solanum lycopersicum). It has been demonstrated that only the gain-of-function allele of Slwo (SlWo(V), the Slwo woolly motif mutant allele) can increase the trichome density; however, it remains unclear why the two alleles function differently in trichome development. In this study, we used Nicotiana benthamiana as a model and cloned the homologues of Slwo and SlCycB2 (named Nbwo and NbCycB2). We also constructed a Nbwo gain-of-function allele with the same mutation site as SlWo(V) (named NbWo(V)). We found that both Nbwo and NbWo(V) directly regulate NbCycB2 and their own expression by binding to the promoter of NbCycB2 and their own genomic sequences. As form of a feedback regulation, NbCycB2 negatively regulates trichome formation by repressing Nbwo activity at the protein level. We also found that mutations in the Nbwo woolly motif can prevent repression of NbWo(V) by NbCycB2, which results in a significant increase in the amount of active Nbwo proteins and in increases in trichome density and the number of branches. Our results reveal a novel reciprocal regulation mechanism between NbCycB2 and Nbwo during trichome formation in N. benthamiana. |
format | Online Article Text |
id | pubmed-7242068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72420682020-05-27 NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development Wu, Min-Liang Cui, Yu-Chao Ge, Li Cui, Li-Peng Xu, Zhi-Chao Zhang, Hong-Ying Wang, Zhao-Jun Zhou, Dan Wu, Shuang Chen, Liang Cui, Hong J Exp Bot Research Papers The transcription factor Woolly (Wo) and its downstream gene CycB2 have been shown to regulate trichome development in tomato (Solanum lycopersicum). It has been demonstrated that only the gain-of-function allele of Slwo (SlWo(V), the Slwo woolly motif mutant allele) can increase the trichome density; however, it remains unclear why the two alleles function differently in trichome development. In this study, we used Nicotiana benthamiana as a model and cloned the homologues of Slwo and SlCycB2 (named Nbwo and NbCycB2). We also constructed a Nbwo gain-of-function allele with the same mutation site as SlWo(V) (named NbWo(V)). We found that both Nbwo and NbWo(V) directly regulate NbCycB2 and their own expression by binding to the promoter of NbCycB2 and their own genomic sequences. As form of a feedback regulation, NbCycB2 negatively regulates trichome formation by repressing Nbwo activity at the protein level. We also found that mutations in the Nbwo woolly motif can prevent repression of NbWo(V) by NbCycB2, which results in a significant increase in the amount of active Nbwo proteins and in increases in trichome density and the number of branches. Our results reveal a novel reciprocal regulation mechanism between NbCycB2 and Nbwo during trichome formation in N. benthamiana. Oxford University Press 2020-03-25 2020-01-28 /pmc/articles/PMC7242068/ /pubmed/31990970 http://dx.doi.org/10.1093/jxb/erz542 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Wu, Min-Liang Cui, Yu-Chao Ge, Li Cui, Li-Peng Xu, Zhi-Chao Zhang, Hong-Ying Wang, Zhao-Jun Zhou, Dan Wu, Shuang Chen, Liang Cui, Hong NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development |
title | NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development |
title_full | NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development |
title_fullStr | NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development |
title_full_unstemmed | NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development |
title_short | NbCycB2 represses Nbwo activity via a negative feedback loop in tobacco trichome development |
title_sort | nbcycb2 represses nbwo activity via a negative feedback loop in tobacco trichome development |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242068/ https://www.ncbi.nlm.nih.gov/pubmed/31990970 http://dx.doi.org/10.1093/jxb/erz542 |
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