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Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production
In the last decade polycistronic vectors have become essential tools for both basic science and gene therapy applications. In order to co-express heterologous polypeptides, different systems have been developed from Internal Ribosome Entry Site (IRES) based vectors to the use of the 2A peptide. Unfo...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777421/ https://www.ncbi.nlm.nih.gov/pubmed/19729510 http://dx.doi.org/10.1093/nar/gkp716 |
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author | Fallot, Stéphanie Ben Naya, Raouia Hieblot, Corinne Mondon, Philippe Lacazette, Eric Bouayadi, Khalil Kharrat, Abdelhakim Touriol, Christian Prats, Hervé |
author_facet | Fallot, Stéphanie Ben Naya, Raouia Hieblot, Corinne Mondon, Philippe Lacazette, Eric Bouayadi, Khalil Kharrat, Abdelhakim Touriol, Christian Prats, Hervé |
author_sort | Fallot, Stéphanie |
collection | PubMed |
description | In the last decade polycistronic vectors have become essential tools for both basic science and gene therapy applications. In order to co-express heterologous polypeptides, different systems have been developed from Internal Ribosome Entry Site (IRES) based vectors to the use of the 2A peptide. Unfortunately, these methods are not fully suitable for the efficient and reproducible modulation of the ratio between the proteins of interest. Here we describe a novel bicistronic vector type based on the use of alternative splicing. By modifying the consensus sequence that governs splicing, we demonstrate that the ratio between the synthesized proteins could easily vary from 1 : 10 to 10 : 1. We have established this system with luciferase genes and we extended its application to the production of recombinant monoclonal antibodies. We have shown that these vectors could be used in several typical cell lines with similar efficiencies. We also present an adaptation of these vectors to hybrid alternative splicing/IRES constructs that allow a ratio-controlled expression of proteins of interest in stably transfected cell lines. |
format | Text |
id | pubmed-2777421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27774212009-11-16 Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production Fallot, Stéphanie Ben Naya, Raouia Hieblot, Corinne Mondon, Philippe Lacazette, Eric Bouayadi, Khalil Kharrat, Abdelhakim Touriol, Christian Prats, Hervé Nucleic Acids Res Methods Online In the last decade polycistronic vectors have become essential tools for both basic science and gene therapy applications. In order to co-express heterologous polypeptides, different systems have been developed from Internal Ribosome Entry Site (IRES) based vectors to the use of the 2A peptide. Unfortunately, these methods are not fully suitable for the efficient and reproducible modulation of the ratio between the proteins of interest. Here we describe a novel bicistronic vector type based on the use of alternative splicing. By modifying the consensus sequence that governs splicing, we demonstrate that the ratio between the synthesized proteins could easily vary from 1 : 10 to 10 : 1. We have established this system with luciferase genes and we extended its application to the production of recombinant monoclonal antibodies. We have shown that these vectors could be used in several typical cell lines with similar efficiencies. We also present an adaptation of these vectors to hybrid alternative splicing/IRES constructs that allow a ratio-controlled expression of proteins of interest in stably transfected cell lines. Oxford University Press 2009-11 2009-09-03 /pmc/articles/PMC2777421/ /pubmed/19729510 http://dx.doi.org/10.1093/nar/gkp716 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Fallot, Stéphanie Ben Naya, Raouia Hieblot, Corinne Mondon, Philippe Lacazette, Eric Bouayadi, Khalil Kharrat, Abdelhakim Touriol, Christian Prats, Hervé Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production |
title | Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production |
title_full | Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production |
title_fullStr | Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production |
title_full_unstemmed | Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production |
title_short | Alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production |
title_sort | alternative-splicing-based bicistronic vectors for ratio-controlled protein expression and application to recombinant antibody production |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2777421/ https://www.ncbi.nlm.nih.gov/pubmed/19729510 http://dx.doi.org/10.1093/nar/gkp716 |
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