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ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber)
BACKGROUND: Gene activity is largely controlled by transcriptional regulation through the action of transcription factors and other regulators. QsMYB1 is a member of the R2R3-MYB transcription factor family related to secondary growth, and in particular, with the cork development process. In order t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142680/ https://www.ncbi.nlm.nih.gov/pubmed/30223777 http://dx.doi.org/10.1186/s12870-018-1403-5 |
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author | Capote, Tiago Barbosa, Pedro Usié, Ana Ramos, António Marcos Inácio, Vera Ordás, Ricardo Gonçalves, Sónia Morais-Cecílio, Leonor |
author_facet | Capote, Tiago Barbosa, Pedro Usié, Ana Ramos, António Marcos Inácio, Vera Ordás, Ricardo Gonçalves, Sónia Morais-Cecílio, Leonor |
author_sort | Capote, Tiago |
collection | PubMed |
description | BACKGROUND: Gene activity is largely controlled by transcriptional regulation through the action of transcription factors and other regulators. QsMYB1 is a member of the R2R3-MYB transcription factor family related to secondary growth, and in particular, with the cork development process. In order to identify the putative gene targets of QsMYB1 across the cork oak genome we developed a ChIP-Seq strategy. RESULTS: Results provide direct evidence that QsMY1B targets genes encoding for enzymes involved in the lignin and suberin pathways as well as gene encoding for ABCG transporters and LTPs implicated in the transport of monomeric suberin units across the cellular membrane. These results highlight the role of QsMYB1 as a regulator of lignin and suberin biosynthesis, transport and assembly. CONCLUSION: To our knowledge, this work constitutes the first ChIP-Seq experiment performed in cork oak, a non-model plant species with a long-life cycle, and these results will contribute to deepen the knowledge about the molecular mechanisms of cork formation and differentiation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1403-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6142680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61426802018-09-21 ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber) Capote, Tiago Barbosa, Pedro Usié, Ana Ramos, António Marcos Inácio, Vera Ordás, Ricardo Gonçalves, Sónia Morais-Cecílio, Leonor BMC Plant Biol Research Article BACKGROUND: Gene activity is largely controlled by transcriptional regulation through the action of transcription factors and other regulators. QsMYB1 is a member of the R2R3-MYB transcription factor family related to secondary growth, and in particular, with the cork development process. In order to identify the putative gene targets of QsMYB1 across the cork oak genome we developed a ChIP-Seq strategy. RESULTS: Results provide direct evidence that QsMY1B targets genes encoding for enzymes involved in the lignin and suberin pathways as well as gene encoding for ABCG transporters and LTPs implicated in the transport of monomeric suberin units across the cellular membrane. These results highlight the role of QsMYB1 as a regulator of lignin and suberin biosynthesis, transport and assembly. CONCLUSION: To our knowledge, this work constitutes the first ChIP-Seq experiment performed in cork oak, a non-model plant species with a long-life cycle, and these results will contribute to deepen the knowledge about the molecular mechanisms of cork formation and differentiation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-018-1403-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-17 /pmc/articles/PMC6142680/ /pubmed/30223777 http://dx.doi.org/10.1186/s12870-018-1403-5 Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Capote, Tiago Barbosa, Pedro Usié, Ana Ramos, António Marcos Inácio, Vera Ordás, Ricardo Gonçalves, Sónia Morais-Cecílio, Leonor ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber) |
title | ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber) |
title_full | ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber) |
title_fullStr | ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber) |
title_full_unstemmed | ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber) |
title_short | ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber) |
title_sort | chip-seq reveals that qsmyb1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (quercus suber) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6142680/ https://www.ncbi.nlm.nih.gov/pubmed/30223777 http://dx.doi.org/10.1186/s12870-018-1403-5 |
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