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A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy
The shoot structure of cultivated grapevine Vitis vinifera L. typically exhibits a three-node modular repetitive pattern, two sequential leaf-opposed tendrils followed by a tendril-free node. In this study, we investigated the molecular basis of this pattern by characterizing differentially expresse...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506248/ https://www.ncbi.nlm.nih.gov/pubmed/28713572 http://dx.doi.org/10.1038/hortres.2017.32 |
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author | Arro, Jie Cuenca, Jose Yang, Yingzhen Liang, Zhenchang Cousins, Peter Zhong, Gan-Yuan |
author_facet | Arro, Jie Cuenca, Jose Yang, Yingzhen Liang, Zhenchang Cousins, Peter Zhong, Gan-Yuan |
author_sort | Arro, Jie |
collection | PubMed |
description | The shoot structure of cultivated grapevine Vitis vinifera L. typically exhibits a three-node modular repetitive pattern, two sequential leaf-opposed tendrils followed by a tendril-free node. In this study, we investigated the molecular basis of this pattern by characterizing differentially expressed genes in 10 bulk samples of young tendril tissue from two grapevine populations showing segregation of mutant or wild-type shoot/tendril phyllotaxy. One population was the selfed progeny and the other one, an outcrossed progeny of a Vitis hybrid, ‘Roger’s Red’. We analyzed 13 375 expressed genes and carried out in-depth analyses of 324 of them, which were differentially expressed with a minimum of 1.5-fold changes between the mutant and wild-type bulk samples in both selfed and cross populations. A significant portion of these genes were direct cis-binding targets of 14 transcription factor families that were themselves differentially expressed. Network-based dependency analysis further revealed that most of the significantly rewired connections among the 10 most connected hub genes involved at least one transcription factor. TCP3 and MYB12, which were known important for plant-form development, were among these transcription factors. More importantly, TCP3 and MYB12 were found in this study to be involved in regulating the lignin gene PRX52, which is important to plant-form development. A further support evidence for the roles of TCP3-MYB12-PRX52 in contributing to tendril phyllotaxy was the findings of two other lignin-related genes uniquely expressed in the mutant phyllotaxy background. |
format | Online Article Text |
id | pubmed-5506248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55062482017-07-14 A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy Arro, Jie Cuenca, Jose Yang, Yingzhen Liang, Zhenchang Cousins, Peter Zhong, Gan-Yuan Hortic Res Article The shoot structure of cultivated grapevine Vitis vinifera L. typically exhibits a three-node modular repetitive pattern, two sequential leaf-opposed tendrils followed by a tendril-free node. In this study, we investigated the molecular basis of this pattern by characterizing differentially expressed genes in 10 bulk samples of young tendril tissue from two grapevine populations showing segregation of mutant or wild-type shoot/tendril phyllotaxy. One population was the selfed progeny and the other one, an outcrossed progeny of a Vitis hybrid, ‘Roger’s Red’. We analyzed 13 375 expressed genes and carried out in-depth analyses of 324 of them, which were differentially expressed with a minimum of 1.5-fold changes between the mutant and wild-type bulk samples in both selfed and cross populations. A significant portion of these genes were direct cis-binding targets of 14 transcription factor families that were themselves differentially expressed. Network-based dependency analysis further revealed that most of the significantly rewired connections among the 10 most connected hub genes involved at least one transcription factor. TCP3 and MYB12, which were known important for plant-form development, were among these transcription factors. More importantly, TCP3 and MYB12 were found in this study to be involved in regulating the lignin gene PRX52, which is important to plant-form development. A further support evidence for the roles of TCP3-MYB12-PRX52 in contributing to tendril phyllotaxy was the findings of two other lignin-related genes uniquely expressed in the mutant phyllotaxy background. Nature Publishing Group 2017-07-12 /pmc/articles/PMC5506248/ /pubmed/28713572 http://dx.doi.org/10.1038/hortres.2017.32 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Arro, Jie Cuenca, Jose Yang, Yingzhen Liang, Zhenchang Cousins, Peter Zhong, Gan-Yuan A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy |
title | A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy |
title_full | A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy |
title_fullStr | A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy |
title_full_unstemmed | A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy |
title_short | A transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy |
title_sort | transcriptome analysis of two grapevine populations segregating for tendril phyllotaxy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5506248/ https://www.ncbi.nlm.nih.gov/pubmed/28713572 http://dx.doi.org/10.1038/hortres.2017.32 |
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