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Progress

CloningTransfectionDoxCytometryData Analyis
LRs transformed    

 

Procedure

TRE

Doxycycline00.1nM1nM10nM100nM1000nM
LacIIPTG00.1mM0.5mM1mM5mM10mM
CumateCumate      
EGSHPonasterone A00.1uM0.5uM1uM5uM10uM

 

Notes: 

Glucose in the media may be a problem with the lac system (glucose is a weak anti-inducer of the lac repressor). A paper found a two fold decrease in induction in cells cultured in glucose containing media compared to galactose substituted media. 

Background 

To determine the optimal level of expression of BCR components and Syk-TEVp, we are placing them under the control of inducible/repressible promoters. This experiment aims to characterize the activity of the promoters we are going to use: TREt and pLac. 

The pLac system may not be ideal to modulate expression given it's quick on/off response. We looked into other inducible expression systems:

EGSH promoter: http://parts.igem.org/Part:BBa_K415507

Cumate promoter: 

http://parts.igem.org/Part:BBa_K875001

RheoSwitch: 

http://66.155.211.155/nebecomm/products_Intl/productE3000.asp

RheoSwitch uses a Gal4 activator and the gene to be expressed is under control of a Gal4 response element. We can't use that because we are already using  gal4 transcriptional activation to mediate receptor activation response. 

Approach

We are going to investigate the expression of mKate driven by each of the promoters with varying concentrations of inducer (dox) and repressor (IPTG).

Parts

PartStatus
hEF1a:rtTA 
TRE:mKate 
pLac:mKate 
hEF1a:LacI 
hEF1a:CymR 
hEF1a-Cuo:mKate 
CMV5-CuO:mKate 
EGSH:mKate 
hEf1a:VgEcR-2A-RXR 

References

Ecsydone responsive promoter:

http://www.biotechniques.com/multimedia/archive/00011/01312rr03_11591a.pdf

other paper

Lac repression system: 

this paper

Cumate induction system:

this one

this link

Data 

Discussion

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