Difference between revisions of "Part:BBa K3861011"

Line 11: Line 11:
 
<html>
 
<html>
 
The sequence contains already an RBS, thus genes that aimed to be expressed from this promoter can be added directly downstream of the submitted sequence.
 
The sequence contains already an RBS, thus genes that aimed to be expressed from this promoter can be added directly downstream of the submitted sequence.
 +
The sequence is derived from Tn10<I>d</I>Tet transposon.
  
 
</html>
 
</html>

Revision as of 23:56, 21 October 2021


tetR-Ptet

Tetracycline inducer system based on the tetracycline resistance mechanism found in gram-negative bacteria.1 It is one of the most used transcriptional regulatory systems.2 We use the Tet-On system where the transcription is induced in the presence of a tetracycline or tetracycline derivates.3 The rtTA (reverse tetracycline transactivator) protein, a fusion of the TetR (tetracycline repressor) and VP16 ativation domain, can bind the TRE (tetracycline response element) only in the presence of tetracycline, thereby activating gene expression.3

Usage and Biology

The sequence contains already an RBS, thus genes that aimed to be expressed from this promoter can be added directly downstream of the submitted sequence. The sequence is derived from Tn10dTet transposon.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


References

1. Orth, P., Schnappinger, D., Hillen, W., Saenger, W. & Hinrichs, W. Structural basis of gene regulation by the tetracycline inducible Tet repressor–operator system. Nat. Struct. Biol. 7, 215–219 (2000).
2. Baron, U. & Bujard, H. Tet repressor-based system for regulated gene expression in eukaryotic cells: principles and advances. Methods Enzymol. 327, 401–421 (2000).
3. Gossen, M. et al. Transcriptional Activation by Tetracyclines in Mammalian Cells. Science 268, 1766–1769 (1995).