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Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors
BACKGROUND: The efficacy and biosafety of lentiviral gene transfer is influenced by the design of the vector. To this end, properties of lentiviral vectors can be modified by using cis-acting elements such as the modification of the U3 region of the LTR, the incorporation of the central flap (cPPT-C...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025823/ https://www.ncbi.nlm.nih.gov/pubmed/21205311 http://dx.doi.org/10.1186/1479-0556-9-1 |
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author | Grandchamp, Nicolas Henriot, Dorothée Philippe, Stéphanie Amar, Lahouari Ursulet, Suzanna Serguera, Che Mallet, Jacques Sarkis, Chamsy |
author_facet | Grandchamp, Nicolas Henriot, Dorothée Philippe, Stéphanie Amar, Lahouari Ursulet, Suzanna Serguera, Che Mallet, Jacques Sarkis, Chamsy |
author_sort | Grandchamp, Nicolas |
collection | PubMed |
description | BACKGROUND: The efficacy and biosafety of lentiviral gene transfer is influenced by the design of the vector. To this end, properties of lentiviral vectors can be modified by using cis-acting elements such as the modification of the U3 region of the LTR, the incorporation of the central flap (cPPT-CTS) element, or post-transcriptional regulatory elements such as the woodchuck post-transcriptional regulatory element (WPRE). Recently, several studies evaluated the influence of the incorporation of insulators into the integrating lentiviral vector genome on transgene expression level and position effects. METHODS: In the present study, the influence of the matrix attachment region (MAR) of the mouse immunoglobulin-κ (Ig-κ) or the chicken lysozyme (ChL) gene was studied on three types of HIV-1-derived lentiviral vectors: self-inactivating (SIN) lentiviral vectors (LV), double-copy lentiviral vectors (DC) and non-integrating lentiviral vectors (NILVs) in different cell types: HeLa, HEK293T, NIH-3T3, Raji, and T Jurkat cell lines and primary neural progenitors. RESULTS AND DISCUSSION: Our results demonstrate that the Ig-κ MAR in the context of LV slightly increases transduction efficiency only in Hela, NIH-3T3 and Jurkat cells. In the context of double-copy lentiviral vectors, the Ig-κ MAR has no effect or even negatively influences transduction efficiency. In the same way, in the context of non-integrating lentiviral vectors, the Ig-κ MAR has no effect or even negatively influences transduction efficiency, except in differentiated primary neural progenitor cells. The ChL MAR in the context of integrating and non-integrating lentiviral vectors shows no effect or a decrease of transgene expression in all tested conditions. CONCLUSIONS: This study demonstrates that MAR sequences not necessarily increase transgene expression and that the effect of these sequences is probably context dependent and/or vector dependent. Thus, this study highlights the importance to consider a MAR sequence in a given context. Moreover, other recent reports pointed out the potential effects of random integration of insulators on the expression level of endogenous genes. Taken together, these results show that the use of an insulator in a vector for gene therapy must be well assessed in the particular therapeutic context that it will be used for, and must be balanced with its potential genotoxic effects. |
format | Text |
id | pubmed-3025823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30258232011-01-25 Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors Grandchamp, Nicolas Henriot, Dorothée Philippe, Stéphanie Amar, Lahouari Ursulet, Suzanna Serguera, Che Mallet, Jacques Sarkis, Chamsy Genet Vaccines Ther Research BACKGROUND: The efficacy and biosafety of lentiviral gene transfer is influenced by the design of the vector. To this end, properties of lentiviral vectors can be modified by using cis-acting elements such as the modification of the U3 region of the LTR, the incorporation of the central flap (cPPT-CTS) element, or post-transcriptional regulatory elements such as the woodchuck post-transcriptional regulatory element (WPRE). Recently, several studies evaluated the influence of the incorporation of insulators into the integrating lentiviral vector genome on transgene expression level and position effects. METHODS: In the present study, the influence of the matrix attachment region (MAR) of the mouse immunoglobulin-κ (Ig-κ) or the chicken lysozyme (ChL) gene was studied on three types of HIV-1-derived lentiviral vectors: self-inactivating (SIN) lentiviral vectors (LV), double-copy lentiviral vectors (DC) and non-integrating lentiviral vectors (NILVs) in different cell types: HeLa, HEK293T, NIH-3T3, Raji, and T Jurkat cell lines and primary neural progenitors. RESULTS AND DISCUSSION: Our results demonstrate that the Ig-κ MAR in the context of LV slightly increases transduction efficiency only in Hela, NIH-3T3 and Jurkat cells. In the context of double-copy lentiviral vectors, the Ig-κ MAR has no effect or even negatively influences transduction efficiency. In the same way, in the context of non-integrating lentiviral vectors, the Ig-κ MAR has no effect or even negatively influences transduction efficiency, except in differentiated primary neural progenitor cells. The ChL MAR in the context of integrating and non-integrating lentiviral vectors shows no effect or a decrease of transgene expression in all tested conditions. CONCLUSIONS: This study demonstrates that MAR sequences not necessarily increase transgene expression and that the effect of these sequences is probably context dependent and/or vector dependent. Thus, this study highlights the importance to consider a MAR sequence in a given context. Moreover, other recent reports pointed out the potential effects of random integration of insulators on the expression level of endogenous genes. Taken together, these results show that the use of an insulator in a vector for gene therapy must be well assessed in the particular therapeutic context that it will be used for, and must be balanced with its potential genotoxic effects. BioMed Central 2011-01-04 /pmc/articles/PMC3025823/ /pubmed/21205311 http://dx.doi.org/10.1186/1479-0556-9-1 Text en Copyright ©2011 Grandchamp et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Grandchamp, Nicolas Henriot, Dorothée Philippe, Stéphanie Amar, Lahouari Ursulet, Suzanna Serguera, Che Mallet, Jacques Sarkis, Chamsy Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors |
title | Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors |
title_full | Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors |
title_fullStr | Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors |
title_full_unstemmed | Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors |
title_short | Influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors |
title_sort | influence of insulators on transgene expression from integrating and non-integrating lentiviral vectors |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025823/ https://www.ncbi.nlm.nih.gov/pubmed/21205311 http://dx.doi.org/10.1186/1479-0556-9-1 |
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