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Reporter Systems

The last step of our overall strategy is to characterize in vivo the affinity and specificity of our TetR mutants. To that end, we set up two reporter systems based on RFP fluorescence.

Skip to details about:

1. Ptet promoter characterization
2. Plac promoter characterization
3. Plasmids details

TetR - RFP system

Description

The first system is the simplest one; it is composed of TetR driven by a constitutive promoter with RFP (red fluorescent protein) under Ptet control. If TetR binds to Ptet, then RFP is repressed. By applying different concentrations of ATC (anhydrotetracycline) to the cells, RFP is expressed - the stronger the TetR mutant binds to Ptet, the higher the ATC concentration needed to have full expression of RFP.

The TetR and RFP genes were put on two different plasmids: pSB3K1 pConst-TetR and J61002 Ptet-RFP. For more details about them, please refer to the [add link once the new page has been created] page.

Experimental validation - with wild-type TetR

ATC induction

To validate our first readout system, we performed platereader experiments with different concentrations of anhydritetracycline (ATC). This molecule binds to the TetR dimers and induces conformational changes that make the transcription factor unable to bind to Ptet. As a result, RFP can be expressed.

Gene expression in the cell without ATC:

Gene expression in the cell with ATC:

Here are the results of our ATC induction experiment:

The induction curves show that RFP indeed increases with addition of TetR. Without any ATC in the medium, cells express about 2500 normalized RFUs when they reach a plateau, whereas with the highest values of ATC we have 25'000 normalized RFUs. There is a 10x difference between normal medium and addition of ATC, showing that our first readout system is effectively powerful. Moreover, expression of RFP in cells without ATC is 10-fold lower than the values obtained for Ptet characterization alone.

We can reasonably assume that this system can actually be used for in vivo screening: TetR mutants that would not recognize the consensus Ptet sequence would yield a lot more RFP expression than other mutants recognizing Ptet.

Dose-response

By looking at the dose-response graph, we can see a significant increase between 0 and 200 ng/microL ATC; then the RFUs are quite stable. The graph shows that the TetR-Ptet interaction has a strong impact on RFP expression. The highest RFUs measured here correspond to the levels of the Ptet-RFP construct alone (without the TetR plasmid), showing that we can get a complete TetR inactivation in our experiment.

TetR mutants characterization

With the wild-type TetR in our system, RFP is repressed because wt-TetR binds to Ptet. However, a mutant that would recognize a completely different sequence as Ptet would be unable to repress RFP, as you can see in the illustartions below:

Gene expression with wild-type TetR:

Gene expression with a TetR mutant not recognizing Ptet:

add platereader results asap

TetR - LacI - RFP system

Description

Our second system contains LacI in addition to TetR and RFP. TetR is still induced by a constitutive promoter, then LacI is under Ptet regulation and RFP is under Plac regulation. LacI plays here the role of an inverter, so that we can measure directly TetR-Ptet interactions: if TetR binds to Ptet, LacI is not expressed, so RFP is not repressed and is instead expressed. Here, the strongest a TetR mutant binds to Ptet, the highest RFP intensity we will get.

Here also we have a two-plasmid system; TetR and LacI are placed on the pSB3K1 Pconst-TetR Ptet-LacI plasmid whereas RFP is on the J61002 Plac-RFP plasmid. You can find more informations about these plasmids on the plasmids details page.

Experimental validation - with wild-type TetR

Our second readout system being based on TetR and LacI, we repressed both sequentially by using respectively ATC and IPTG.

ATC induction

Adding ATC in the medium of the co-transformed cells will inactivate TetR. As a consequence, LacI will be expressed and RFP will be repressed. We should then see a decrease of RFUs correlating with increasing concentrations of ATC.

Gene expression in the cells without ATC:

Gene expression in the cells with ATC:

Below you can see the induction curves with different ATC concentrations added in the cell's medium:

With no or low concentrations of IPTG in the cells' medium, RFP expression is quite weak; this can be explained by the fact that Ptet was mutated in our plasmids and thus TetR couldn't repress LacI very efficiently. In normal conditions, we should see RFP expression when TetR binds to Ptet - which is the case here, since we have the wild-type TetR gene. Here, LacI not well repressed by TetR, thus RFP is repressed even when TetR binds to Ptet. Nevertheless, there is a decrease in RFP expression when we add sufficient amounts of ATC. Even in our mutated system, TetR interaction to Ptet still has an effect on the output. There is a 2-fold difference between high ATC concentrations and no ATC; we believe that, by restoring Ptet sequence, this difference would be higher.

ATC dose-response curve

This data shows more clearly the difference of normalized RFUs for low or high concentrations of ATC - even if the intensities are low. As in our first readout system, the highest ATC efficiency seems to be reached with 200 ng/microL already.

IPTG induction

IPTG will inactivate LacI, so that RFP will be more expressed. The expected results are an increase of RFUs in parallel of an increase of IPTG concentration in the medium.

Gene expression in the cell without IPTG:

Gene expression in the cell with IPTG:

Below you can see the induction curves with different IPTG concentrations added in the cell's medium:

Indeed,RFUs increase 8-fold between no IPTG and the highest concentrations. Note that the RFU intensity for the curve with no IPTG matches the intensity of the curve with no ATC in the ATC induction experiment, showing that these two experiments are consistent. The curves with the highest IPTG concentrations are not overlapping, showing that perhaps we could repress LacI in a more efficient manner if we used higher IPTG concentrations.

You can compare these results with the characterization of Plac alone. Without IPTG, RFP expression is much lower than the real Plac strength; our system does react strongly to LacI expression.

IPTG dose-response curve

Even if the RFU range is small, there is a clear parallel between RFUs intensities and IPTG dosage. An 8-fold difference between the two extremes can be sufficient for an effective and reliable readout system; however we could use a stronger Plac promoter to get more RFP expression and perhaps a bigger difference.