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Graded or threshold response of the tet-controlled gene expression: all depends on the concentration of the transactivator.
- Source :
-
BMC biotechnology [BMC Biotechnol] 2013 Jan 22; Vol. 13, pp. 5. Date of Electronic Publication: 2013 Jan 22. - Publication Year :
- 2013
-
Abstract
- Background: Currently, the step-wise integration of tet-dependent transactivator and tet-responsive expression unit is considered to be the most promising tool to achieve stable tet-controlled gene expression in cell populations. However, disadvantages of this strategy for integration into primary cells led us to develop an "All-In-One" vector system, enabling simultaneous integration of both components. The effect on tet-controlled gene expression was analyzed for retroviral "All-In-One" vectors expressing the M2-transactivator either under control of a constitutive or a new type of autoregulated promoter.<br />Results: Determination of luciferase activity in transduced cell populations indicated improvement of the dynamic range of gene expression for the autoregulated system. Further differences were observed regarding induction kinetics and dose-response. Most notably, introduction of the autoregulated system resulted in a threshold mode of induction, whereas the constitutive system exhibited pronounced effector-dose dependence.<br />Conclusion: Tet-regulated gene expression in the applied autoregulated system resembles a threshold mode, whereby full induction of the tet-unit can be achieved at otherwise limiting doxycycline concentrations.
- Subjects :
- Cell Line
Genetic Vectors genetics
HeLa Cells
Humans
Kinetics
Luciferases genetics
Luciferases metabolism
Promoter Regions, Genetic
Proviruses genetics
Trans-Activators genetics
Transduction, Genetic
Doxycycline pharmacology
Gene Expression drug effects
Genetic Vectors metabolism
Trans-Activators metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1472-6750
- Volume :
- 13
- Database :
- MEDLINE
- Journal :
- BMC biotechnology
- Publication Type :
- Academic Journal
- Accession number :
- 23336718
- Full Text :
- https://doi.org/10.1186/1472-6750-13-5