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A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins

BACKGROUND: Transient gene expression is a powerful tool to study gene function in plants. In citrus, Agrobacterium transformation is the method of choice for transient expression studies, but this method does not work efficiently with many gene constructs, and there is a need for a more robust tran...

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Autores principales: Levy, Amit, El-Mochtar, Choaa, Wang, Chunxia, Goodin, Michael, Orbovic, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759842/
https://www.ncbi.nlm.nih.gov/pubmed/29339969
http://dx.doi.org/10.1186/s13007-017-0270-7
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author Levy, Amit
El-Mochtar, Choaa
Wang, Chunxia
Goodin, Michael
Orbovic, Vladimir
author_facet Levy, Amit
El-Mochtar, Choaa
Wang, Chunxia
Goodin, Michael
Orbovic, Vladimir
author_sort Levy, Amit
collection PubMed
description BACKGROUND: Transient gene expression is a powerful tool to study gene function in plants. In citrus, Agrobacterium transformation is the method of choice for transient expression studies, but this method does not work efficiently with many gene constructs, and there is a need for a more robust transient expression system in citrus leaves. Biolistic particle delivery is an alternative to Agrobacterium transformation, and in some plants, such as Arabidopsis, gives higher transformation rates in leaf tissues than Agrobacterium. RESULTS: Here we describe an improved method for gene expression in epidermal cells of citrus leaves, using the Bio-Rad Helios gene-gun. Gene-gun bombardment of GFP-HDEL produced highly efficient gene expression in large number of cells and in different citrus varieties. We show here that transiently expressed proteins have maintained their functions in plants, and this is demonstrated by the subcellular localization of different organelle markers, and by a functional assay of Xanthomonas citri effector AvrGF1. To further expand the available tools for subcellular localization studies in citrus, we also generated a new set of transgenic citrus plants that contain organelle markers labelling the nuclei, actin and endoplasmic reticulum. Using these new tools, we were able to show that the coat protein of citrus tristeza virus localizes to the cytoplasm and nuclei when expressed in epidermal cells fused to GFP. CONCLUSION: We have optimized a new method for transient expression in citrus leaves, to give highly reproducible and efficient transformation without producing a high level of injury or artifacts to the bombarded tissue. We also generated the first set organelle markers for use in citrus. These fluorescent protein markers label the nucleus and the actin. With these new resources, protein activity and subcellular localization can be studied in citrus rapidly and in high throughput. The handheld gene-gun device can also be used in the grove to deliver therapies for citrus diseases, such as canker and Huanglongbing, into trees. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-017-0270-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-57598422018-01-16 A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins Levy, Amit El-Mochtar, Choaa Wang, Chunxia Goodin, Michael Orbovic, Vladimir Plant Methods Methodology BACKGROUND: Transient gene expression is a powerful tool to study gene function in plants. In citrus, Agrobacterium transformation is the method of choice for transient expression studies, but this method does not work efficiently with many gene constructs, and there is a need for a more robust transient expression system in citrus leaves. Biolistic particle delivery is an alternative to Agrobacterium transformation, and in some plants, such as Arabidopsis, gives higher transformation rates in leaf tissues than Agrobacterium. RESULTS: Here we describe an improved method for gene expression in epidermal cells of citrus leaves, using the Bio-Rad Helios gene-gun. Gene-gun bombardment of GFP-HDEL produced highly efficient gene expression in large number of cells and in different citrus varieties. We show here that transiently expressed proteins have maintained their functions in plants, and this is demonstrated by the subcellular localization of different organelle markers, and by a functional assay of Xanthomonas citri effector AvrGF1. To further expand the available tools for subcellular localization studies in citrus, we also generated a new set of transgenic citrus plants that contain organelle markers labelling the nuclei, actin and endoplasmic reticulum. Using these new tools, we were able to show that the coat protein of citrus tristeza virus localizes to the cytoplasm and nuclei when expressed in epidermal cells fused to GFP. CONCLUSION: We have optimized a new method for transient expression in citrus leaves, to give highly reproducible and efficient transformation without producing a high level of injury or artifacts to the bombarded tissue. We also generated the first set organelle markers for use in citrus. These fluorescent protein markers label the nucleus and the actin. With these new resources, protein activity and subcellular localization can be studied in citrus rapidly and in high throughput. The handheld gene-gun device can also be used in the grove to deliver therapies for citrus diseases, such as canker and Huanglongbing, into trees. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-017-0270-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-09 /pmc/articles/PMC5759842/ /pubmed/29339969 http://dx.doi.org/10.1186/s13007-017-0270-7 Text en © The Author(s) 2018 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
Levy, Amit
El-Mochtar, Choaa
Wang, Chunxia
Goodin, Michael
Orbovic, Vladimir
A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins
title A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins
title_full A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins
title_fullStr A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins
title_full_unstemmed A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins
title_short A new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins
title_sort new toolset for protein expression and subcellular localization studies in citrus and its application to citrus tristeza virus proteins
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5759842/
https://www.ncbi.nlm.nih.gov/pubmed/29339969
http://dx.doi.org/10.1186/s13007-017-0270-7
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