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An efficient transient expression system for gene function analysis in rose

BACKGROUND: Roses are widely used as garden ornamental plants and cut flowers. Rosa chinensis cv ‘Old Blush’ has been used as a model genotype in rose studies due to its contribution to recurrent flowering and tea scent traits of modern roses. The deficiency of efficient genetic transformation syste...

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Autores principales: Lu, Jun, Bai, Mengjuan, Ren, Haoran, Liu, Jinyi, Wang, Changquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740963/
https://www.ncbi.nlm.nih.gov/pubmed/29299050
http://dx.doi.org/10.1186/s13007-017-0268-1
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author Lu, Jun
Bai, Mengjuan
Ren, Haoran
Liu, Jinyi
Wang, Changquan
author_facet Lu, Jun
Bai, Mengjuan
Ren, Haoran
Liu, Jinyi
Wang, Changquan
author_sort Lu, Jun
collection PubMed
description BACKGROUND: Roses are widely used as garden ornamental plants and cut flowers. Rosa chinensis cv ‘Old Blush’ has been used as a model genotype in rose studies due to its contribution to recurrent flowering and tea scent traits of modern roses. The deficiency of efficient genetic transformation systems is a handicap limiting functional genetics studies of roses. Agrobacterium-mediated transient transformation offers a powerful tool for the characterization of gene function in plants. RESULTS: A convenient and highly efficient Agrobacterium mediated genetic transformation protocol using R. chinensis cv ‘Old Blush’ seedlings in vitro as an expression system is described in this paper. The most important factor affecting transformation efficiency in this system is seedling age; 3/4-week-old rose shoots with or without roots from sub-culturing are optimal for transformation, requiring no complicated inoculation media, supplements, or carefully tuned plant growth conditions. This transient expression system was successfully applied to analysis of the gene promoter activities, DNA binding capacity of transcription factors, protein–protein interaction in physiological contexts using luciferase as a reporter gene. CONCLUSIONS: This transient transformation system was validated as a robust and efficient platform, thus providing a new option for gene function and signaling pathway investigation in roses and further extending the utility of R. chinensis cv ‘Old Blush’ as a model plant to study diverse gene function and signaling pathways in Rosaceae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-017-0268-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-57409632018-01-03 An efficient transient expression system for gene function analysis in rose Lu, Jun Bai, Mengjuan Ren, Haoran Liu, Jinyi Wang, Changquan Plant Methods Methodology BACKGROUND: Roses are widely used as garden ornamental plants and cut flowers. Rosa chinensis cv ‘Old Blush’ has been used as a model genotype in rose studies due to its contribution to recurrent flowering and tea scent traits of modern roses. The deficiency of efficient genetic transformation systems is a handicap limiting functional genetics studies of roses. Agrobacterium-mediated transient transformation offers a powerful tool for the characterization of gene function in plants. RESULTS: A convenient and highly efficient Agrobacterium mediated genetic transformation protocol using R. chinensis cv ‘Old Blush’ seedlings in vitro as an expression system is described in this paper. The most important factor affecting transformation efficiency in this system is seedling age; 3/4-week-old rose shoots with or without roots from sub-culturing are optimal for transformation, requiring no complicated inoculation media, supplements, or carefully tuned plant growth conditions. This transient expression system was successfully applied to analysis of the gene promoter activities, DNA binding capacity of transcription factors, protein–protein interaction in physiological contexts using luciferase as a reporter gene. CONCLUSIONS: This transient transformation system was validated as a robust and efficient platform, thus providing a new option for gene function and signaling pathway investigation in roses and further extending the utility of R. chinensis cv ‘Old Blush’ as a model plant to study diverse gene function and signaling pathways in Rosaceae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-017-0268-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-22 /pmc/articles/PMC5740963/ /pubmed/29299050 http://dx.doi.org/10.1186/s13007-017-0268-1 Text en © The Author(s) 2017 Open AccessThis 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 Methodology
Lu, Jun
Bai, Mengjuan
Ren, Haoran
Liu, Jinyi
Wang, Changquan
An efficient transient expression system for gene function analysis in rose
title An efficient transient expression system for gene function analysis in rose
title_full An efficient transient expression system for gene function analysis in rose
title_fullStr An efficient transient expression system for gene function analysis in rose
title_full_unstemmed An efficient transient expression system for gene function analysis in rose
title_short An efficient transient expression system for gene function analysis in rose
title_sort efficient transient expression system for gene function analysis in rose
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740963/
https://www.ncbi.nlm.nih.gov/pubmed/29299050
http://dx.doi.org/10.1186/s13007-017-0268-1
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