Part:BBa_I759019:Design
cis7-repressed, tet-regulated YFP
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 985
Illegal NheI site found at 1008 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This part is the YFP sequence down-regulated by the cis repressive element. The Ptet promoter and TetR gene, which is under the control of a constitutive promoter, establish an inducible system in which transcription can be activated by the addition of anhydrotetracycline (aTc).
Cis7 is a modified version of constructs made by the University of California Berkeley iGEM 2006 team. Modifications involve a change in the number of bulges and end-loop size which affect the free energy of interaction within the cis structure. The key principal in the design was to find a structure that offered tight repression of the gene of interest but also allowed for activation upon addition of a trans-activating element. A lower free energy indicates tighter binding and a decreased favorability for forming a compliment with the trans element. The cis7 construct was designed to be activated by trans4. Design specifics: free energy = -16.3kcal; 8bp loop, 4 bulges, 5bp toe-hold
Source
Caltech iGEM 2007. The cr element is a synthetic oligo which has been inserted into part I759009.
References
http://parts2.mit.edu/wiki/index.php/University_of_California_Berkeley_2006