Cargando…
Development of expression vectors based on pepino mosaic virus
BACKGROUND: Plant viruses are useful expression vectors because they can mount systemic infections allowing large amounts of recombinant protein to be produced rapidly in differentiated plant tissues. Pepino mosaic virus (PepMV) (genus Potexvirus, family Flexiviridae), a widespread plant virus, is a...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065447/ https://www.ncbi.nlm.nih.gov/pubmed/21396092 http://dx.doi.org/10.1186/1746-4811-7-6 |
_version_ | 1782200983502192640 |
---|---|
author | Sempere, Raquel N Gómez, Pedro Truniger, Verónica Aranda, Miguel A |
author_facet | Sempere, Raquel N Gómez, Pedro Truniger, Verónica Aranda, Miguel A |
author_sort | Sempere, Raquel N |
collection | PubMed |
description | BACKGROUND: Plant viruses are useful expression vectors because they can mount systemic infections allowing large amounts of recombinant protein to be produced rapidly in differentiated plant tissues. Pepino mosaic virus (PepMV) (genus Potexvirus, family Flexiviridae), a widespread plant virus, is a promising candidate expression vector for plants because of its high level of accumulation in its hosts and the absence of severe infection symptoms. We report here the construction of a stable and efficient expression vector for plants based on PepMV. RESULTS: Agroinfectious clones were produced from two different PepMV genotypes (European and Chilean), and these were able to initiate typical PepMV infections. We explored several strategies for vector development including coat protein (CP) replacement, duplication of the CP subgenomic promoter (SGP) and the creation of a fusion protein using the foot-and-mouth disease virus (FMDV) 2A catalytic peptide. We found that CP replacement vectors were unable to move systemically and that vectors with duplicated SGPs (even heterologous SGPs) suffered from significant transgene instability. The fusion protein incorporating the FMDV 2A catalytic peptide gave by far the best results, maintaining stability through serial passages and allowing the accumulation of GFP to 0.2-0.4 g per kg of leaf tissue. The possible use of PepMV as a virus-induced gene silencing vector to study gene function was also demonstrated. Protocols for the use of this vector are described. CONCLUSIONS: A stable PepMV vector was generated by expressing the transgene as a CP fusion using the sequence encoding the foot-and-mouth disease virus (FMDV) 2A catalytic peptide to separate them. We have generated a novel tool for the expression of recombinant proteins in plants and for the functional analysis of virus and plant genes. Our experiments have also highlighted virus requirements for replication in single cells as well as intercellular and long-distance movement. |
format | Text |
id | pubmed-3065447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30654472011-03-29 Development of expression vectors based on pepino mosaic virus Sempere, Raquel N Gómez, Pedro Truniger, Verónica Aranda, Miguel A Plant Methods Methodology BACKGROUND: Plant viruses are useful expression vectors because they can mount systemic infections allowing large amounts of recombinant protein to be produced rapidly in differentiated plant tissues. Pepino mosaic virus (PepMV) (genus Potexvirus, family Flexiviridae), a widespread plant virus, is a promising candidate expression vector for plants because of its high level of accumulation in its hosts and the absence of severe infection symptoms. We report here the construction of a stable and efficient expression vector for plants based on PepMV. RESULTS: Agroinfectious clones were produced from two different PepMV genotypes (European and Chilean), and these were able to initiate typical PepMV infections. We explored several strategies for vector development including coat protein (CP) replacement, duplication of the CP subgenomic promoter (SGP) and the creation of a fusion protein using the foot-and-mouth disease virus (FMDV) 2A catalytic peptide. We found that CP replacement vectors were unable to move systemically and that vectors with duplicated SGPs (even heterologous SGPs) suffered from significant transgene instability. The fusion protein incorporating the FMDV 2A catalytic peptide gave by far the best results, maintaining stability through serial passages and allowing the accumulation of GFP to 0.2-0.4 g per kg of leaf tissue. The possible use of PepMV as a virus-induced gene silencing vector to study gene function was also demonstrated. Protocols for the use of this vector are described. CONCLUSIONS: A stable PepMV vector was generated by expressing the transgene as a CP fusion using the sequence encoding the foot-and-mouth disease virus (FMDV) 2A catalytic peptide to separate them. We have generated a novel tool for the expression of recombinant proteins in plants and for the functional analysis of virus and plant genes. Our experiments have also highlighted virus requirements for replication in single cells as well as intercellular and long-distance movement. BioMed Central 2011-03-11 /pmc/articles/PMC3065447/ /pubmed/21396092 http://dx.doi.org/10.1186/1746-4811-7-6 Text en Copyright ©2011 Sempere et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Sempere, Raquel N Gómez, Pedro Truniger, Verónica Aranda, Miguel A Development of expression vectors based on pepino mosaic virus |
title | Development of expression vectors based on pepino mosaic virus |
title_full | Development of expression vectors based on pepino mosaic virus |
title_fullStr | Development of expression vectors based on pepino mosaic virus |
title_full_unstemmed | Development of expression vectors based on pepino mosaic virus |
title_short | Development of expression vectors based on pepino mosaic virus |
title_sort | development of expression vectors based on pepino mosaic virus |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065447/ https://www.ncbi.nlm.nih.gov/pubmed/21396092 http://dx.doi.org/10.1186/1746-4811-7-6 |
work_keys_str_mv | AT sempereraqueln developmentofexpressionvectorsbasedonpepinomosaicvirus AT gomezpedro developmentofexpressionvectorsbasedonpepinomosaicvirus AT trunigerveronica developmentofexpressionvectorsbasedonpepinomosaicvirus AT arandamiguela developmentofexpressionvectorsbasedonpepinomosaicvirus |