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Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin

BACKGROUND: Lupins are promising protein crops with an increasing amount of genomic and transcriptomic resources. The new resources facilitate the in silico identification of candidate genes controlling important agronomic traits. However, a major bottleneck for lupin research and crop improvement i...

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Autores principales: Mancinotti, Davide, Rodriguez, Maria Cecilia, Frick, Karen Michiko, Dueholm, Bjørn, Jepsen, Ditte Goldschmidt, Agerbirk, Niels, Geu-Flores, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8714437/
https://www.ncbi.nlm.nih.gov/pubmed/34963500
http://dx.doi.org/10.1186/s13007-021-00832-4
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author Mancinotti, Davide
Rodriguez, Maria Cecilia
Frick, Karen Michiko
Dueholm, Bjørn
Jepsen, Ditte Goldschmidt
Agerbirk, Niels
Geu-Flores, Fernando
author_facet Mancinotti, Davide
Rodriguez, Maria Cecilia
Frick, Karen Michiko
Dueholm, Bjørn
Jepsen, Ditte Goldschmidt
Agerbirk, Niels
Geu-Flores, Fernando
author_sort Mancinotti, Davide
collection PubMed
description BACKGROUND: Lupins are promising protein crops with an increasing amount of genomic and transcriptomic resources. The new resources facilitate the in silico identification of candidate genes controlling important agronomic traits. However, a major bottleneck for lupin research and crop improvement is the in planta characterization of gene function. Here, we present an efficient protocol for virus-induced gene silencing (VIGS) to down-regulate endogenous genes in narrow-leafed lupin (NLL) using the apple latent spherical virus (ALSV). RESULTS: We identified ALSV as an appropriate VIGS vector able to infect NLL without causing a discernible phenotype. We created improved ALSV vectors to allow for efficient cloning of gene fragments into the viral genome and for easier viral propagation via agroinfiltration of Nicotiana benthamiana. Using this system, we silenced the visual marker gene phytoene desaturase (PDS), which resulted in systemic, homogenous silencing as indicated by bleaching of newly produced tissues. Furthermore, by silencing lysine decarboxylase (LaLDC)—a gene likely to be involved in toxic alkaloid biosynthesis—we demonstrate the applicability of our VIGS method to silence a target gene alone or alongside PDS in a ‘PDS co-silencing’ approach. The co-silencing approach allows the visual identification of tissues where silencing is actively occurring, which eases tissue harvesting and downstream analysis, and is useful where the trait under study is not affected by PDS silencing. Silencing LaLDC resulted in a ~ 61% or ~ 67% decrease in transcript level, depending on whether LaLDC was silenced alone or alongside PDS. Overall, the silencing of LaLDC resulted in reduced alkaloid levels, providing direct evidence of its involvement in alkaloid biosynthesis in NLL. CONCLUSIONS: We provide a rapid and efficient VIGS method for validating gene function in NLL. This will accelerate the research and improvement of this underutilized crop. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-021-00832-4.
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spelling pubmed-87144372022-01-05 Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin Mancinotti, Davide Rodriguez, Maria Cecilia Frick, Karen Michiko Dueholm, Bjørn Jepsen, Ditte Goldschmidt Agerbirk, Niels Geu-Flores, Fernando Plant Methods Research BACKGROUND: Lupins are promising protein crops with an increasing amount of genomic and transcriptomic resources. The new resources facilitate the in silico identification of candidate genes controlling important agronomic traits. However, a major bottleneck for lupin research and crop improvement is the in planta characterization of gene function. Here, we present an efficient protocol for virus-induced gene silencing (VIGS) to down-regulate endogenous genes in narrow-leafed lupin (NLL) using the apple latent spherical virus (ALSV). RESULTS: We identified ALSV as an appropriate VIGS vector able to infect NLL without causing a discernible phenotype. We created improved ALSV vectors to allow for efficient cloning of gene fragments into the viral genome and for easier viral propagation via agroinfiltration of Nicotiana benthamiana. Using this system, we silenced the visual marker gene phytoene desaturase (PDS), which resulted in systemic, homogenous silencing as indicated by bleaching of newly produced tissues. Furthermore, by silencing lysine decarboxylase (LaLDC)—a gene likely to be involved in toxic alkaloid biosynthesis—we demonstrate the applicability of our VIGS method to silence a target gene alone or alongside PDS in a ‘PDS co-silencing’ approach. The co-silencing approach allows the visual identification of tissues where silencing is actively occurring, which eases tissue harvesting and downstream analysis, and is useful where the trait under study is not affected by PDS silencing. Silencing LaLDC resulted in a ~ 61% or ~ 67% decrease in transcript level, depending on whether LaLDC was silenced alone or alongside PDS. Overall, the silencing of LaLDC resulted in reduced alkaloid levels, providing direct evidence of its involvement in alkaloid biosynthesis in NLL. CONCLUSIONS: We provide a rapid and efficient VIGS method for validating gene function in NLL. This will accelerate the research and improvement of this underutilized crop. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-021-00832-4. BioMed Central 2021-12-28 /pmc/articles/PMC8714437/ /pubmed/34963500 http://dx.doi.org/10.1186/s13007-021-00832-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mancinotti, Davide
Rodriguez, Maria Cecilia
Frick, Karen Michiko
Dueholm, Bjørn
Jepsen, Ditte Goldschmidt
Agerbirk, Niels
Geu-Flores, Fernando
Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin
title Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin
title_full Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin
title_fullStr Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin
title_full_unstemmed Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin
title_short Development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin
title_sort development and application of a virus-induced gene silencing protocol for the study of gene function in narrow-leafed lupin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8714437/
https://www.ncbi.nlm.nih.gov/pubmed/34963500
http://dx.doi.org/10.1186/s13007-021-00832-4
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