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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...

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Detalles Bibliográficos
Autores principales: Kang, Kang, Huang, Lian, Li, Qing, Liao, Xiaoyun, Dang, Quanjin, Yang, Yi, Luo, Jun, Zeng, Yan, Li, Li, Gou, Deming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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
Descripción
Sumario: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.