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Tet-On Systems For Doxycycline-inducible Gene Expression
The tetracycline-controlled Tet-Off and Tet-On gene expression systems are used to regulate the activity of genes in eukaryotic cells in diverse settings, varying from basic biological research to biotechnology and gene therapy applications. These systems are based on regulatory elements that contro...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070417/ https://www.ncbi.nlm.nih.gov/pubmed/27216914 http://dx.doi.org/10.2174/1566523216666160524144041 |
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author | Das, Atze T. Tenenbaum, Liliane Berkhout, Ben |
author_facet | Das, Atze T. Tenenbaum, Liliane Berkhout, Ben |
author_sort | Das, Atze T. |
collection | PubMed |
description | The tetracycline-controlled Tet-Off and Tet-On gene expression systems are used to regulate the activity of genes in eukaryotic cells in diverse settings, varying from basic biological research to biotechnology and gene therapy applications. These systems are based on regulatory elements that control the activity of the tetracycline-resistance operon in bacteria. The Tet-Off system allows silencing of gene expression by administration of tetracycline (Tc) or tetracycline-derivatives like doxycycline (dox), whereas the Tet-On system allows activation of gene expression by dox. Since the initial design and construction of the original Tet-system, these bacterium-derived systems have been significantly improved for their function in eukaryotic cells. We here review how a dox-controlled HIV-1 variant was designed and used to greatly improve the activity and dox-sensitivity of the rtTA transcriptional activator component of the Tet-On system. These optimized rtTA variants require less dox for activation, which will reduce side effects and allow gene control in tissues where a relatively low dox level can be reached, such as the brain. |
format | Online Article Text |
id | pubmed-5070417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-50704172016-11-14 Tet-On Systems For Doxycycline-inducible Gene Expression Das, Atze T. Tenenbaum, Liliane Berkhout, Ben Curr Gene Ther Article The tetracycline-controlled Tet-Off and Tet-On gene expression systems are used to regulate the activity of genes in eukaryotic cells in diverse settings, varying from basic biological research to biotechnology and gene therapy applications. These systems are based on regulatory elements that control the activity of the tetracycline-resistance operon in bacteria. The Tet-Off system allows silencing of gene expression by administration of tetracycline (Tc) or tetracycline-derivatives like doxycycline (dox), whereas the Tet-On system allows activation of gene expression by dox. Since the initial design and construction of the original Tet-system, these bacterium-derived systems have been significantly improved for their function in eukaryotic cells. We here review how a dox-controlled HIV-1 variant was designed and used to greatly improve the activity and dox-sensitivity of the rtTA transcriptional activator component of the Tet-On system. These optimized rtTA variants require less dox for activation, which will reduce side effects and allow gene control in tissues where a relatively low dox level can be reached, such as the brain. Bentham Science Publishers 2016-06 2016-06 /pmc/articles/PMC5070417/ /pubmed/27216914 http://dx.doi.org/10.2174/1566523216666160524144041 Text en © 2016 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) ( https://creativecommons.org/licenses/by-nc/4.0/legalcode ), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Das, Atze T. Tenenbaum, Liliane Berkhout, Ben Tet-On Systems For Doxycycline-inducible Gene Expression |
title | Tet-On Systems For Doxycycline-inducible Gene Expression |
title_full | Tet-On Systems For Doxycycline-inducible Gene Expression |
title_fullStr | Tet-On Systems For Doxycycline-inducible Gene Expression |
title_full_unstemmed | Tet-On Systems For Doxycycline-inducible Gene Expression |
title_short | Tet-On Systems For Doxycycline-inducible Gene Expression |
title_sort | tet-on systems for doxycycline-inducible gene expression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070417/ https://www.ncbi.nlm.nih.gov/pubmed/27216914 http://dx.doi.org/10.2174/1566523216666160524144041 |
work_keys_str_mv | AT dasatzet tetonsystemsfordoxycyclineinduciblegeneexpression AT tenenbaumliliane tetonsystemsfordoxycyclineinduciblegeneexpression AT berkhoutben tetonsystemsfordoxycyclineinduciblegeneexpression |