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− | <div style='background: #808080; margin: 0px | + | <div style='background: #808080; margin: 0px 14% 20px 14%; height:1px;></div> |
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− | <div style='background: #808080; margin: 0px | + | <div style='background: #808080; margin: 0px 14% 20px 14%; height:1px;></div> |
<div style='padding-top: 0px;'></div> | <div style='padding-top: 0px;'></div> | ||
− | <div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | + | <div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' >A simple example of a dynamical circuit is the incoherent feed forward loop (IFFL), which consists of three proteins X, Y, and Z which regulate each other such that X activates Y and Z, and Y represses Z. This circuit architecture can generate a pulsatile response upon activation of X (Figure 1). |
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<img src='https://static.igem.org/mediawiki/2017/3/31/T--William_and_Mary--IFFL-Pulse-example.png' width = "50%"/> | <img src='https://static.igem.org/mediawiki/2017/3/31/T--William_and_Mary--IFFL-Pulse-example.png' width = "50%"/> | ||
− | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: | + | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: 14px;'>Figure 1: Schematic of an Incoherent Feedforward Loop (IFFL) circuit. X, Y, and Z represent arbitrary transcription factors. At t=0, the production of X is activated. In region (1), the molecules of X activate the production of both Z and Y. However, the concentration of Y is insufficient to significantly repress the production of Z, so its concentration increases. In region (2), the concentration of Y has grown sufficiently large that it now exerts a significant repressive effect on the production of Z. This causes the concentration of Z to decrease. In region (3), the repressive effect from Y and the activating effect from X have balanced and the circuit has reached its steady state. |
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<div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | <div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | ||
− | By tuning the properties of the different interactions within the circuit, one can control the overall dynamics of its response. For example, there are several ways to control the sharpness of the pulse in the circuit’s temporal response. One approach is to increase the strength of Y’s repression of Z (Figure 2, red arrow). This will cause the circuit’s relaxation to | + | By tuning the properties of the different interactions within the circuit, one can control the overall dynamics of its response. For example, there are several ways to control the sharpness of the pulse in the circuit’s temporal response. One approach is to increase the strength of Y’s repression of Z (Figure 2, red arrow). This will cause the circuit’s relaxation to steady state to occur more quickly, narrowing the width of the pulse. One could also increase the speed of X’s activation of Z (Figure 2, green arrow), which increases the slope of the circuit’s initial rise to its peak. |
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− | <img src='https://static.igem.org/mediawiki/2017/9/9c/T--William_and_Mary--IFFL-Figure2.png' width = " | + | <img src='https://static.igem.org/mediawiki/2017/9/9c/T--William_and_Mary--IFFL-Figure2.png' width = "45%"/> |
− | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: | + | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: 14px;'>Figure 2: Tuning dynamical properties of the pulsatile response of the IFFL circuit. (Red Arrow) Increasing the strength of the repression of Z by Y causes the width of the pulse to decrease, as the speed of the transition from the pulse peak to the steady state is set by Y’s repression of Z. (Green Arrow) Increasing the speed of the activation of Z by X causes the circuit to rise faster to its peak. The result of these effects is a sharpening of the pulse. |
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<div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | <div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | ||
− | Using the Lon-pdt system, we constructed a minimal IFFL circuit which relies on Lon’s proteolytic degradation of a pdt-tagged reporter as the circuit’s inhibition step (Figure 3). By choosing to use Lon as the middle Y protein in the IFFL, we place both the Y-Z inhibition strength and the X-Z activation strengths under the control of the same property— the strength of the pdt on Z. Because the sharpness of the pulse is now driven by the strength of Lon’s activity, we predict that by swapping out different choices of pdt on the tagged reporter we will be able to control the sharpness of the circuit’s pulse | + | Using the Lon-pdt system, we constructed a minimal IFFL circuit which relies on Lon’s proteolytic degradation of a pdt-tagged reporter as the circuit’s inhibition step (Figure 3). By choosing to use Lon as the middle inhibitor (Y) protein in the IFFL, we place both the Y-Z inhibition strength and the X-Z activation strengths under the control of the same property— the strength of the pdt on Z. Because the sharpness of the pulse is now driven by the strength of Lon’s activity, we predict that by swapping out different choices of pdt on the tagged reporter we will be able to control the sharpness of the circuit’s pulse.. </div> |
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− | <img src='https://static.igem.org/mediawiki/2017/c/c6/T--William_and_Mary--Lon_IFFL_structure.png' width = " | + | <img src='https://static.igem.org/mediawiki/2017/c/c6/T--William_and_Mary--Lon_IFFL_structure.png' width = "50%"/> |
− | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: | + | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: 14px;'>Figure 3: Schematic of the Lon-based IFFL. The simultaneous induction of the circuit with ATC and IPTG serves as a proxy for the activation of the single protein X in the canonical IFFL circuit. mf-Lon is under basal repression by lacI and mScarlet is under basal respression by tetR, so neither protein is produced until the inducers are present. As long as ATC and IPTG are introduced into the cell at the same time, the fundamental structure of the IFFL is preserved. |
</div></figcaption> | </div></figcaption> | ||
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<div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | <div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | ||
− | However, we were concerned that our Lon-based circuit might be too unorthodox to function effectively as a pulse-generating IFFL. Although we can diagram our circuit in a way that takes the form of an IFFL’s structure, both the fact that we are including small-molecule inducers as a node in the circuit and the fact that our Y-Z inhibition step is realized by post-translational degradation | + | However, we were concerned that our Lon-based circuit might be too unorthodox to function effectively as a pulse-generating IFFL. Although we can diagram our circuit in a way that takes the form of an IFFL’s structure, both the fact that we are including small-molecule inducers as a node in the circuit and the fact that our Y-Z inhibition step is realized by post-translational degradation rather than transcriptional repression, are unconventional choices which are not often seen in the canonical descriptions of IFFL circuits. Therefore, to confirm our intuition that our Lon-based circuit would function as a valid IFFL, we simulated an ODE model of our circuit over a wide range of parameters to investigate the types of responses which the circuit can generate (Figure 4). We found that our circuit can exhibit a wide range of responses, all of which are characteristic of an IFFL circuit’s behavior. With this result, we were confident that the design of our circuit was sound, and we moved on to experimentally measure its behavior. |
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<figure style='padding-left: px;'> | <figure style='padding-left: px;'> | ||
<img src='https://static.igem.org/mediawiki/2017/9/93/T--William_and_Mary--IFFL-Model-Trace.png' width = "60%"/> | <img src='https://static.igem.org/mediawiki/2017/9/93/T--William_and_Mary--IFFL-Model-Trace.png' width = "60%"/> | ||
− | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: | + | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: 14px;'>Figure 4: Some example timecourses from our ODE model of the Lon-based IFFL circuit. Our circuit is able to generate pulses of various sharpness, as well as more standard relaxation responses, all of which correspond to the behavior of a canonical IFFL. The simulations were performed by taking our protease complexing model [see <a href='https://2017.igem.org/Team:William_and_Mary/Model' style='color: #808080; text-decoration: underline;'>Modeling</a> section] and setting the initial conditions so that Lon and the reporter are activated simultaneously. |
</div></figcaption> | </div></figcaption> | ||
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− | <img src='https://static.igem.org/mediawiki/2017/8/8b/T--William_and_Mary--IFFL-pdtA.png' width = " | + | <img src='https://static.igem.org/mediawiki/2017/8/8b/T--William_and_Mary--IFFL-pdtA.png' width = "50%"/> |
− | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: | + | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: 14px;'>Figure 5: The Lon-based IFFL circuit can exhibit a pulsatile response. The pulsatile response should only be present in the simultaneous induction condition, as otherwise the circuit does not satisfy the structure of an IFFL. The circuit was constructed using ATC-activatable mScarlet tagged with pdt A (BBa_K2333428) on pSB1C3 and IPTG-activatable mf-Lon (BBa_K2333434) on pSB3K3. NEB 10-beta cells in M9 media with 0.4% glucose and 0.1% casamino acids were induced with 50 ng/mL ATC at t=0, along with 0.1 mM IPTG at t=0 (simultaneous Lon induction) or t= -4 hrs (pre-induced Lon) and their absolute fluorescence levels were measured with FACS at 20 minute intervals. These fluorescence values were then normalized by their maxima. Shaded regions represent one geometric SD factor above and below the geometric mean of 3 biological replicates. |
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<figure style='padding-left: px;'> | <figure style='padding-left: px;'> | ||
<img src='https://static.igem.org/mediawiki/2017/3/3d/T--William_and_Mary--speed_is_preserved.png' width = "70%"/> | <img src='https://static.igem.org/mediawiki/2017/3/3d/T--William_and_Mary--speed_is_preserved.png' width = "70%"/> | ||
− | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: | + | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: 14px;'>Figure 6: The increased speed from the pdt system is preserved in the simultaneous induction case. (A) Pre-inducing Lon to steady state before the activation of mScarlet allows one to observe a faster speed to steady state, as expected. (B) The pdt-tagged circuit is faster than the untagged circuit even in the case of simultaneous Lon induction. Experimental conditions and data processing procedures are as in Figure 5. |
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− | <img src='https://static.igem.org/mediawiki/2017/4/4f/T--William_and_Mary--mScarlet-I_Speed_Normalized_Full.png' width = " | + | <img src='https://static.igem.org/mediawiki/2017/4/4f/T--William_and_Mary--mScarlet-I_Speed_Normalized_Full.png' width = "50%"/> |
− | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: | + | <figcaption><div style='padding-left: 20%;padding-right:20%; padding-top: 15px; color: #808080; font-size: 14px;'>Fig 7: The IFFL’s pulse sharpens with increasing pdt strength. All experimental and data processing conditions are as in Fig 5. |
</figure> | </figure> | ||
</center> | </center> | ||
<div style="padding-top: 40px;"></div> | <div style="padding-top: 40px;"></div> | ||
− | <div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' > | + | <div style = 'padding-right: 14%; padding-left: 14%; text-indent: 50px;line-height: 25px;' >We have demonstrated that by using the pdt system’s control over a single gene’s expression speed, we can exert predictable control over an emergent dynamical property of a genetic circuit simply through the modular swapping of a single genetic part. We anticipate that additional dynamical properties such as the period and amplitude of oscillations, the threshold and duration of temporal buffering, the properties of a signal integrator, and many more will all be amenable to predictable control through the pdt system. |
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Latest revision as of 03:39, 2 November 2017