Highly inducible dual-promoter lentiviral TET-ON system
The invention relates to expression systems useful for regulated expression of a gene of interest based on the constitutive expression of the original TetR repressor and the expression of the polynucleotide driven by a constitutive promoter operably linked to an operator sequence for a tetracycline operator sequence. The system can be provided as two different polynucleotides or as an all-in-one vector. The invention also relates to vectors, host cells and viral particles according to the invention as well as to the uses thereof for in vitro and in vivo production of products of interest or for therapy.
1. A polynucleotide comprising
(i) a transcriptional regulatory sequence comprising a first promoter and at least one binding site for a transcriptional repressor wherein said first promoter and said at least one binding site for a transcriptional repressor are arranged so that the binding of a transcriptional repressor to said at least one binding site inhibits a transcriptional activity of the promoter and
(ii) an expression cassette comprising a polynucleotide encoding a regulatable transcriptional repressor under the operative control of a second promoter wherein said regulatable transcriptional repressor is capable of specifically binding to the at least one binding site in the transcriptional regulatory sequence in the absence but not in the presence of a ligand thereof
wherein the second promoter is an elongation factor 1α (EF1α) promoter, and wherein the first promoter is a cytomegalovirus (CMV) intermediate early promoter.
2. The polynucleotide according to claim 1 wherein the at least one binding site for a transcriptional repressor comprises at least a TetO operator sequence and wherein the regulatabie transcriptional repressor k a tetracycline repressor.
3. The polynucleotide according to claim 1 wherein the at least one binding site for the transcriptional repressor is downstream of the first promoter.
4. The polynucleotide according to claim 1 wherein the regulatable transcriptional repressor further comprises a nuclear localization signal.
5. The polynucleotide according to claim 1 further comprising a polynucleotide of interest under operative control of the transcriptional regulatory sequence.
6. An expression vector comprising the polynucleotide according to claim 1 .
7. A lentiviral particle comprising the vector of claim 6 .
8. A host cell comprising the vector of claim 6 .
9. A method for regulating the expression of a nucleic add sequence of interest comprising the steps of
(i) providing a host cell comprising the polynucleotide according to claim 1 wherein the nucleic add sequence of interest is operatively linked to the first promoter in said polynucleotide, and
(ii) contacting said host cell which with a ligand for the transcriptional repressor wherein said ligand is capable of binding to the transcriptional repressor producing an inactive repressor which is released from its binding site in the transcriptional regulatory sequence thereby allowing the transcription of the nucleic acid sequence of interest driven by the first promoter.
10. A method for the treatment of a disease which requires the expression of a polynucleotide of interest in a subject in need thereof which comprises administering to said subject the polynucleotide according to claim 1 wherein the polynucleotide of interest is under operative control of the transcriptional regulatory sequence.
11. A composition or kit-of-parts comprising
(i) a first polynucleotide comprising transcriptional regulatory sequence comprising a first promoter and at least one binding site for a transcriptional repressor wherein said first promoter and said at least one binding site are arranged so that the binding of a transcriptional repressor to said at least one binding site inhibits a transcriptional activity of the promoter, and
(ii) a second polynucleotide comprising an expression cassette comprising a polynucleotide encoding a regulatable transcriptional repressor under the operative control of a second promoter wherein said regulatable transcriptional repressor is capable of specifically binding to the at least one binding site in the transcriptional regulatory sequence in the absence but not in the presence of a ligand thereof
wherein the second promoter is an elongation factor 1α (EF1α) promoter, and wherein the first promoter is a cytomegalovirus (CMV) intermediate early promoter.
12. The composition or kit-of-parts according to claim 11 wherein the at least one binding site for a transcriptional repressor is a binding site for a tetracycline repressor and wherein the regulatable transcriptional repressor is the tetracycline repressor.
13. The composition or kit-of-parts according to claim 12 wherein the at least one binding site for the tetracycline repressor k a TetO operator sequence.
14. The composition or kit-of-parts according to claim 11 further comprising a ligand of the transcriptional repressor capable which, when bound to the repressor, results in an inactive repressor which is no longer capable of binding to its binding site in the transcriptional regulatory sequence.
15. A method for regulating the expression of a nucleic acid sequence of interest comprising the steps of
(i) providing a host cell comprising the first and second polynucleotides of the composition according to claim 11 wherein the nucleic acid is operatively linked to the first promoter of the first polynucleotide, and
(ii) contacting said host cell which with a ligand for the transcriptional repressor wherein said ligand is capable of binding to the transcriptional repressor producing an inactive repressor which is released from its binding site in the transcriptional regulatory sequence thereby allowing the transcription of the nucleic acid sequence of interest driven by the first promoter.
16. A method for the treatment of a disease which requires the expression of a polynucleotide of interest in a subject in need thereof which comprises administering to said subject the composition according to claim 11 wherein the polynucleotide of interest k under operative control of the transcriptional regulatory sequence.