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An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing
BACKGROUND: Tetracycline (Tet)-regulated expression system has become a widely applied tool to control gene activity. This study aimed to improve the Tet-on system with superior regulatory characteristics. RESULTS: By comprehensively comparing factors of transactivators, Tet-responsive elements (TRE...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556963/ https://www.ncbi.nlm.nih.gov/pubmed/31198556 http://dx.doi.org/10.1186/s40104-019-0354-5 |
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author | Kang, Kang Huang, Lian Li, Qing Liao, Xiaoyun Dang, Quanjin Yang, Yi Luo, Jun Zeng, Yan Li, Li Gou, Deming |
author_facet | Kang, Kang Huang, Lian Li, Qing Liao, Xiaoyun Dang, Quanjin Yang, Yi Luo, Jun Zeng, Yan Li, Li Gou, Deming |
author_sort | Kang, Kang |
collection | PubMed |
description | BACKGROUND: Tetracycline (Tet)-regulated expression system has become a widely applied tool to control gene activity. This study aimed to improve the Tet-on system with superior regulatory characteristics. RESULTS: By comprehensively comparing factors of transactivators, Tet-responsive elements (TREs), orientations of induced expression cassette, and promoters controlling the transactivator, we developed an optimal Tet-on system with enhanced inducible efficiency and lower leakiness. With the system, we successfully performed effective inducible and reversible expression of microRNA, and presented a more precise and easily reproducible fine-tuning for confirming the target of a miRNA. Finally, the system was applied in CRISPR/Cas9-mediated knockout of nuclear factor of activated T cells-5 (NFAT5), a protective transcription factor in cellular osmoregulation. CONCLUSIONS: This study established an improved Tet-on system for powerful and stringent gene regulation in functional genetic studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0354-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6556963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65569632019-06-13 An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing Kang, Kang Huang, Lian Li, Qing Liao, Xiaoyun Dang, Quanjin Yang, Yi Luo, Jun Zeng, Yan Li, Li Gou, Deming J Anim Sci Biotechnol Research BACKGROUND: Tetracycline (Tet)-regulated expression system has become a widely applied tool to control gene activity. This study aimed to improve the Tet-on system with superior regulatory characteristics. RESULTS: By comprehensively comparing factors of transactivators, Tet-responsive elements (TREs), orientations of induced expression cassette, and promoters controlling the transactivator, we developed an optimal Tet-on system with enhanced inducible efficiency and lower leakiness. With the system, we successfully performed effective inducible and reversible expression of microRNA, and presented a more precise and easily reproducible fine-tuning for confirming the target of a miRNA. Finally, the system was applied in CRISPR/Cas9-mediated knockout of nuclear factor of activated T cells-5 (NFAT5), a protective transcription factor in cellular osmoregulation. CONCLUSIONS: This study established an improved Tet-on system for powerful and stringent gene regulation in functional genetic studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40104-019-0354-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-10 /pmc/articles/PMC6556963/ /pubmed/31198556 http://dx.doi.org/10.1186/s40104-019-0354-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Kang, Kang Huang, Lian Li, Qing Liao, Xiaoyun Dang, Quanjin Yang, Yi Luo, Jun Zeng, Yan Li, Li Gou, Deming An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing |
title | An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing |
title_full | An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing |
title_fullStr | An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing |
title_full_unstemmed | An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing |
title_short | An improved Tet-on system in microRNA overexpression and CRISPR/Cas9-mediated gene editing |
title_sort | improved tet-on system in microrna overexpression and crispr/cas9-mediated gene editing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556963/ https://www.ncbi.nlm.nih.gov/pubmed/31198556 http://dx.doi.org/10.1186/s40104-019-0354-5 |
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