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Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots
AIM: We report the construction of a Virus-Induced Gene Silencing (VIGS) vector and an agroinoculation protocol for gene silencing in cassava (Manihot esculenta Crantz) leaves and roots. The African cassava mosaic virus isolate from Nigeria (ACMV-[NOg]), which was initially cloned in a binary vector...
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/PMC6109987/ https://www.ncbi.nlm.nih.gov/pubmed/30154909 http://dx.doi.org/10.1186/s13007-018-0340-5 |
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author | Lentz, Ezequiel Matias Kuon, Joel-Elias Alder, Adrian Mangel, Nathalie Zainuddin, Ima M. McCallum, Emily Jane Anjanappa, Ravi Bodampalli Gruissem, Wilhelm Vanderschuren, Hervé |
author_facet | Lentz, Ezequiel Matias Kuon, Joel-Elias Alder, Adrian Mangel, Nathalie Zainuddin, Ima M. McCallum, Emily Jane Anjanappa, Ravi Bodampalli Gruissem, Wilhelm Vanderschuren, Hervé |
author_sort | Lentz, Ezequiel Matias |
collection | PubMed |
description | AIM: We report the construction of a Virus-Induced Gene Silencing (VIGS) vector and an agroinoculation protocol for gene silencing in cassava (Manihot esculenta Crantz) leaves and roots. The African cassava mosaic virus isolate from Nigeria (ACMV-[NOg]), which was initially cloned in a binary vector for agroinoculation assays, was modified for application as VIGS vector. The functionality of the VIGS vector was validated in Nicotiana benthamiana and subsequently applied in wild-type and transgenic cassava plants expressing the uidA gene under the control of the CaMV 35S promoter in order to facilitate the visualization of gene silencing in root tissues. VIGS vectors were targeted to the Mg2+-chelatase gene in wild type plants and both the coding and promoter sequences of the 35S::uidA transgene in transgenic plants to induce silencing. We established an efficient agro-inoculation method with the hyper-virulent Agrobacterium tumefaciens strain AGL1, which allows high virus infection rates. The method can be used as a low-cost and rapid high-throughput evaluation of gene function in cassava leaves, fibrous roots and storage roots. BACKGROUND: VIGS is a powerful tool to trigger transient sequence-specific gene silencing in planta. Gene silencing in different organs of cassava plants, including leaves, fibrous and storage roots, is useful for the analysis of gene function. RESULTS: We developed an African cassava mosaic virus—based VIGS vector as well as a rapid and efficient agro-inoculation protocol to inoculate cassava plants. The VIGS vector was validated by targeting endogenous genes from Nicotiana benthamiana and cassava as well as the uidA marker gene in transgenic cassava for visualization of gene silencing in cassava leaves and roots. CONCLUSIONS: The African cassava mosaic virus—based VIGS vector allows efficient and cost-effective inoculation of cassava for high-throughput analysis of gene function in cassava leaves and roots. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0340-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6109987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61099872018-08-28 Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots Lentz, Ezequiel Matias Kuon, Joel-Elias Alder, Adrian Mangel, Nathalie Zainuddin, Ima M. McCallum, Emily Jane Anjanappa, Ravi Bodampalli Gruissem, Wilhelm Vanderschuren, Hervé Plant Methods Methodology AIM: We report the construction of a Virus-Induced Gene Silencing (VIGS) vector and an agroinoculation protocol for gene silencing in cassava (Manihot esculenta Crantz) leaves and roots. The African cassava mosaic virus isolate from Nigeria (ACMV-[NOg]), which was initially cloned in a binary vector for agroinoculation assays, was modified for application as VIGS vector. The functionality of the VIGS vector was validated in Nicotiana benthamiana and subsequently applied in wild-type and transgenic cassava plants expressing the uidA gene under the control of the CaMV 35S promoter in order to facilitate the visualization of gene silencing in root tissues. VIGS vectors were targeted to the Mg2+-chelatase gene in wild type plants and both the coding and promoter sequences of the 35S::uidA transgene in transgenic plants to induce silencing. We established an efficient agro-inoculation method with the hyper-virulent Agrobacterium tumefaciens strain AGL1, which allows high virus infection rates. The method can be used as a low-cost and rapid high-throughput evaluation of gene function in cassava leaves, fibrous roots and storage roots. BACKGROUND: VIGS is a powerful tool to trigger transient sequence-specific gene silencing in planta. Gene silencing in different organs of cassava plants, including leaves, fibrous and storage roots, is useful for the analysis of gene function. RESULTS: We developed an African cassava mosaic virus—based VIGS vector as well as a rapid and efficient agro-inoculation protocol to inoculate cassava plants. The VIGS vector was validated by targeting endogenous genes from Nicotiana benthamiana and cassava as well as the uidA marker gene in transgenic cassava for visualization of gene silencing in cassava leaves and roots. CONCLUSIONS: The African cassava mosaic virus—based VIGS vector allows efficient and cost-effective inoculation of cassava for high-throughput analysis of gene function in cassava leaves and roots. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0340-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-27 /pmc/articles/PMC6109987/ /pubmed/30154909 http://dx.doi.org/10.1186/s13007-018-0340-5 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 Lentz, Ezequiel Matias Kuon, Joel-Elias Alder, Adrian Mangel, Nathalie Zainuddin, Ima M. McCallum, Emily Jane Anjanappa, Ravi Bodampalli Gruissem, Wilhelm Vanderschuren, Hervé Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots |
title | Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots |
title_full | Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots |
title_fullStr | Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots |
title_full_unstemmed | Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots |
title_short | Cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots |
title_sort | cassava geminivirus agroclones for virus-induced gene silencing in cassava leaves and roots |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109987/ https://www.ncbi.nlm.nih.gov/pubmed/30154909 http://dx.doi.org/10.1186/s13007-018-0340-5 |
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