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A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean

BACKGROUND: Soybean gene functions cannot be easily interrogated through transgenic disruption (knock-out) of genes-of-interest, or transgenic overexpression of proteins-of-interest, because soybean transformation is time-consuming and technically challenging. An attractive alternative is to adminis...

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Autores principales: Zaulda, Fides Angeli, Yang, Seung Hyun, Han, Junping, Mlotshwa, Sizolwenkosi, Dorrance, Anne, Qu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617382/
https://www.ncbi.nlm.nih.gov/pubmed/36307846
http://dx.doi.org/10.1186/s13007-022-00950-7
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author Zaulda, Fides Angeli
Yang, Seung Hyun
Han, Junping
Mlotshwa, Sizolwenkosi
Dorrance, Anne
Qu, Feng
author_facet Zaulda, Fides Angeli
Yang, Seung Hyun
Han, Junping
Mlotshwa, Sizolwenkosi
Dorrance, Anne
Qu, Feng
author_sort Zaulda, Fides Angeli
collection PubMed
description BACKGROUND: Soybean gene functions cannot be easily interrogated through transgenic disruption (knock-out) of genes-of-interest, or transgenic overexpression of proteins-of-interest, because soybean transformation is time-consuming and technically challenging. An attractive alternative is to administer transient gene silencing or overexpression with a plant virus-based vector. However, existing virus-induced gene silencing (VIGS) and/or overexpression vectors suitable for soybean have various drawbacks that hinder their widespread adoption. RESULTS: We describe the development of a new vector based on cowpea severe mosaic virus (CPSMV), a plus-strand RNA virus with its genome divided into two RNA segments, RNA1 and RNA2. This vector, designated FZ, incorporates a cloning site in the RNA2 cDNA, permitting insertion of nonviral sequences. When paired with an optimized RNA1 construct, FZ readily infects both Nicotiana benthamiana and soybean. As a result, FZ constructs destined for soybean can be first delivered to N. benthamiana in order to propagate the modified viruses to high titers. FZ-based silencing constructs induced robust silencing of phytoene desaturase genes in N. benthamiana, multiple soybean accessions, and cowpea. Meanwhile, FZ supported systemic expression of fluorescent proteins mNeonGreen and mCherry in N. benthamiana and soybean. Finally, FZ-mediated expression of the Arabidopsis transcription factor MYB75 caused N. benthamiana to bear brown leaves and purple, twisted flowers, indicating that MYB75 retained the function of activating anthocyanin synthesis pathways in a different plant. CONCLUSIONS: The new CPSMV-derived FZ vector provides a convenient and versatile soybean functional genomics tool that is expected to accelerate the characterization of soybean genes controlling crucial productivity traits. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-022-00950-7.
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spelling pubmed-96173822022-10-30 A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean Zaulda, Fides Angeli Yang, Seung Hyun Han, Junping Mlotshwa, Sizolwenkosi Dorrance, Anne Qu, Feng Plant Methods Research BACKGROUND: Soybean gene functions cannot be easily interrogated through transgenic disruption (knock-out) of genes-of-interest, or transgenic overexpression of proteins-of-interest, because soybean transformation is time-consuming and technically challenging. An attractive alternative is to administer transient gene silencing or overexpression with a plant virus-based vector. However, existing virus-induced gene silencing (VIGS) and/or overexpression vectors suitable for soybean have various drawbacks that hinder their widespread adoption. RESULTS: We describe the development of a new vector based on cowpea severe mosaic virus (CPSMV), a plus-strand RNA virus with its genome divided into two RNA segments, RNA1 and RNA2. This vector, designated FZ, incorporates a cloning site in the RNA2 cDNA, permitting insertion of nonviral sequences. When paired with an optimized RNA1 construct, FZ readily infects both Nicotiana benthamiana and soybean. As a result, FZ constructs destined for soybean can be first delivered to N. benthamiana in order to propagate the modified viruses to high titers. FZ-based silencing constructs induced robust silencing of phytoene desaturase genes in N. benthamiana, multiple soybean accessions, and cowpea. Meanwhile, FZ supported systemic expression of fluorescent proteins mNeonGreen and mCherry in N. benthamiana and soybean. Finally, FZ-mediated expression of the Arabidopsis transcription factor MYB75 caused N. benthamiana to bear brown leaves and purple, twisted flowers, indicating that MYB75 retained the function of activating anthocyanin synthesis pathways in a different plant. CONCLUSIONS: The new CPSMV-derived FZ vector provides a convenient and versatile soybean functional genomics tool that is expected to accelerate the characterization of soybean genes controlling crucial productivity traits. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13007-022-00950-7. BioMed Central 2022-10-28 /pmc/articles/PMC9617382/ /pubmed/36307846 http://dx.doi.org/10.1186/s13007-022-00950-7 Text en © The Author(s) 2022 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
Zaulda, Fides Angeli
Yang, Seung Hyun
Han, Junping
Mlotshwa, Sizolwenkosi
Dorrance, Anne
Qu, Feng
A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean
title A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean
title_full A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean
title_fullStr A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean
title_full_unstemmed A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean
title_short A cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean
title_sort cowpea severe mosaic virus-based vector simplifies virus-induced gene silencing and foreign protein expression in soybean
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617382/
https://www.ncbi.nlm.nih.gov/pubmed/36307846
http://dx.doi.org/10.1186/s13007-022-00950-7
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