Team:Evry/auxin detection
From 2012.igem.org
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<td>µM.min<sup>-1</sup></td> | <td>µM.min<sup>-1</sup></td> | ||
<td>Transcription rate for <i>tir1</i> and <i>gfp-aid-nls</i></td> | <td>Transcription rate for <i>tir1</i> and <i>gfp-aid-nls</i></td> | ||
- | <td>[ | + | <td>[1]</td> |
</tr> | </tr> | ||
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<td>min<sup>-1</sup></td> | <td>min<sup>-1</sup></td> | ||
<td>Degradation rate of mRNA for TIR1 and GFP-AID</td> | <td>Degradation rate of mRNA for TIR1 and GFP-AID</td> | ||
- | <td>[ | + | <td>[1]</td> |
</tr> | </tr> | ||
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<td>min<sup>-1</sup></td> | <td>min<sup>-1</sup></td> | ||
<td>Translation rate constant for mRNA-TIR1 and mRNA-GFP-AID</td> | <td>Translation rate constant for mRNA-TIR1 and mRNA-GFP-AID</td> | ||
- | <td>[ | + | <td>[1]</td> |
</tr> | </tr> | ||
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<td>min<sup>-1</sup></td> | <td>min<sup>-1</sup></td> | ||
<td>Degradation rate for TIR1 </td> | <td>Degradation rate for TIR1 </td> | ||
- | <td>[ | + | <td>[1]</td> |
</tr> | </tr> | ||
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<td>min<sup>-1</sup></td> | <td>min<sup>-1</sup></td> | ||
<td>Degradation rate for GFP-AID</td> | <td>Degradation rate for GFP-AID</td> | ||
- | <td>[ | + | <td>[2]</td> |
</tr> | </tr> | ||
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<td>min<sup>-1</sup></td> | <td>min<sup>-1</sup></td> | ||
<td>Degradation rate constant of compound IAA</td> | <td>Degradation rate constant of compound IAA</td> | ||
- | <td>[ | + | <td>[3]</td> |
</tr> | </tr> | ||
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<td>k<sub>A</sub></td> | <td>k<sub>A</sub></td> | ||
<td>100</td> | <td>100</td> | ||
- | <td>min<sup>-1</sup></td> | + | <td>µM.min<sup>-1</sup></td> |
<td>Association rate for auxin (IAA) and TIR1 </td> | <td>Association rate for auxin (IAA) and TIR1 </td> | ||
- | <td>[ | + | <td>[4]</td> |
</tr> | </tr> | ||
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<td>k<sub>-A</sub></td> | <td>k<sub>-A</sub></td> | ||
<td>1</td> | <td>1</td> | ||
- | <td> | + | <td>min<sup>-1</sup></td> |
<td>Dissociation rate for auxin (IAA) and TIR1</td> | <td>Dissociation rate for auxin (IAA) and TIR1</td> | ||
- | <td>[ | + | <td>[4]</td> |
</tr> | </tr> | ||
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<td>k<sub>G</sub></td> | <td>k<sub>G</sub></td> | ||
<td>0.5</td> | <td>0.5</td> | ||
- | <td>µM</td> | + | <td>µM.min<sup>-1</sup></td> |
<td>Association rate for IAA:TIR1 complex and GFP-AID</td> | <td>Association rate for IAA:TIR1 complex and GFP-AID</td> | ||
- | <td>[ | + | <td>[4]</td> |
</tr> | </tr> | ||
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<td>k<sub>-G</sub></td> | <td>k<sub>-G</sub></td> | ||
<td>0.1</td> | <td>0.1</td> | ||
- | <td> | + | <td>min<sup>-1</sup></td> |
<td>Dissociation rate for IAA:TIR1 complex and GFP-AID</td> | <td>Dissociation rate for IAA:TIR1 complex and GFP-AID</td> | ||
- | <td>[ | + | <td>[4]</td> |
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<td>min<sup>-1</sup></td> | <td>min<sup>-1</sup></td> | ||
<td>Ubiquitination rate of IAA:TIR1 complex to GFP-AID</td> | <td>Ubiquitination rate of IAA:TIR1 complex to GFP-AID</td> | ||
- | <td>[ | + | <td>[4]</td> |
</tr> | </tr> | ||
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<td>cm.min<sup>-1</sup></td> | <td>cm.min<sup>-1</sup></td> | ||
<td>Permeability of plasma membrane for IAA </td> | <td>Permeability of plasma membrane for IAA </td> | ||
- | <td>[ | + | <td>[3]</td> |
</tr> | </tr> | ||
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<td>cm</td> | <td>cm</td> | ||
<td>Thickness of plasma membrane in <i>Xenopus</i> cells </td> | <td>Thickness of plasma membrane in <i>Xenopus</i> cells </td> | ||
- | <td>[ | + | <td>[5]</td> |
</tr> | </tr> | ||
</table> | </table> | ||
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- | + | <p id="references">References:</p> | |
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- | < | + | <li>Paulsen, M., Legewie, S., Eils, R., Karaulanov, E. & Niehrs, C. 2011. Negative feedback in the bone morphogenetic protein 4 (BMP4) synexpression group governs its dynamic signaling range and canalizes development. PNAS 108, 10202-10207 (Supporting Information Appendixm ,SI Table 1. Kinetic parameters of the model).</li> |
- | + | <li>Nicolas Pollet's data </li> | |
- | + | <li>Urakami, M., Ano, R., Kimura, Y., Shima, M., Matsuno, R., Ueno, T. & Akamatsu, M. (2003). Relationship between structure and permeability of tryptophan derivatives across human intestinal epithelial (Caco-2) cells. Zeitschrift für Naturforschung C, Journal of biosciences 58c, 135-42.</li> | |
- | + | <li> </li> | |
- | + | <li>Schillers, H., Danker, T., Schnittler, H.-J., Lang, F. & Oberleithner, H. (2000). Plasma Membrane Plasticity of Xenopus laevis Oocyte Imaged with Atomic Force Microscopy. Cellular Physiol Biochem 10, 1-9.</li> | |
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Revision as of 02:48, 27 October 2012
Auxin detection
Overview
Now that we’ve managed to model auxin creation and transport, you may be asking yourself ; great, those guys have done all those models, but how can we link it to what we see ? That’s the aim of this model that will link the quantity of auxin transported into the cell to GFP degradation that we can observe in our tadpole’s cells. As for us, this model will also help our biologists to find the conditions upon which the reception can work and the help them guess the reasons of possible dysfunction in the auxin reception. Very schematically, this is what's happening during auxin detection:
Once TIR and GFP are produced and auxin has entered the cell, it binds with TIR and then this complex degrades GFP. This is what we're going to model.
Assumptions
In these reactions, we assimilate the complex Auxin-TIR to an enzyme that is able to degrade the GFP. Auxin would then be its activator.
The degradation rate of GFP is negligible; indeed a molecule of GFP takes 72 hours to degrade normally, whereas during auxin detection the complex auxin-TIR degrades it in less than an hour.
The Tir protein is continuously produced and degraded in the cell,
Model Description
Equations
- tir1: open reading frame encoding the protein TIR1 coming from the plantOryza sativa
- gfp-aid-nls: open reading frame encoding the protein GFP fused to auxin-inducible degron (AID) system followed by an SV40 nuclear localization signal
- mRNA-TIR1: mRNA coding the protein TIR1
- mRNA-GFP-AID-NLS: mRNA coding the fused protein GFP-AID-NLS
- TIR1: F-box transport inhibitor response 1 protein
- GFP-AID: Green fluorescence protein fused to auxin-inducible degron system
- degGFP-AID: degraded green fluorescence protein fused to auxin-inducible degron system
- dIAA: diffused indole-3-acetic acid (auxin)
- IAA: Indole-3-acetic acid or auxin
Parameters
Name | Value | Unit | Descrition | Reference |
---|---|---|---|---|
Pr | 1 | µM.min-1 | Transcription rate for tir1 and gfp-aid-nls | [1] |
dmRNA | 0.017 | min-1 | Degradation rate of mRNA for TIR1 and GFP-AID | [1] |
Kz | 1 | min-1 | Translation rate constant for mRNA-TIR1 and mRNA-GFP-AID | [1] |
dprotein | 0.0017 | min-1 | Degradation rate for TIR1 | [1] |
dGFP | 0.001 | min-1 | Degradation rate for GFP-AID | [2] |
dcompound | 0.0013 | min-1 | Degradation rate constant of compound IAA | [3] |
kA | 100 | µM.min-1 | Association rate for auxin (IAA) and TIR1 | [4] |
k-A | 1 | min-1 | Dissociation rate for auxin (IAA) and TIR1 | [4] |
kG | 0.5 | µM.min-1 | Association rate for IAA:TIR1 complex and GFP-AID | [4] |
k-G | 0.1 | min-1 | Dissociation rate for IAA:TIR1 complex and GFP-AID | [4] |
kcat | 5.10-4 | min-1 | Ubiquitination rate of IAA:TIR1 complex to GFP-AID | [4] |
p | 6.10-5 | cm.min-1 | Permeability of plasma membrane for IAA | [3] |
th | 5.10-7 | cm | Thickness of plasma membrane in Xenopus cells | [5] |
References:
- Paulsen, M., Legewie, S., Eils, R., Karaulanov, E. & Niehrs, C. 2011. Negative feedback in the bone morphogenetic protein 4 (BMP4) synexpression group governs its dynamic signaling range and canalizes development. PNAS 108, 10202-10207 (Supporting Information Appendixm ,SI Table 1. Kinetic parameters of the model).
- Nicolas Pollet's data
- Urakami, M., Ano, R., Kimura, Y., Shima, M., Matsuno, R., Ueno, T. & Akamatsu, M. (2003). Relationship between structure and permeability of tryptophan derivatives across human intestinal epithelial (Caco-2) cells. Zeitschrift für Naturforschung C, Journal of biosciences 58c, 135-42.
- Schillers, H., Danker, T., Schnittler, H.-J., Lang, F. & Oberleithner, H. (2000). Plasma Membrane Plasticity of Xenopus laevis Oocyte Imaged with Atomic Force Microscopy. Cellular Physiol Biochem 10, 1-9.