McGill

From 2007.igem.org

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== The Team ==
== The Team ==
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[[McGill/Team Roster| Team Roster]]<br>
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[[McGill/Team Roster| The Team]]<br>
[[McGill/Mailing List|Mailing List]]
[[McGill/Mailing List|Mailing List]]
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== Pictures ==
== Pictures ==
[http://www.flickr.com/photos/cumbers/archives/date-posted/2007/08/21/ Brown University Meetup]  (External) <br>
[http://www.flickr.com/photos/cumbers/archives/date-posted/2007/08/21/ Brown University Meetup]  (External) <br>
[[McGill/Team pics|Team Awesome Oscillators]]<br>
[[McGill/Team pics|Team Awesome Oscillators]]<br>
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Revision as of 00:50, 14 October 2007

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The official wiki of the McGill University iGEM 2007 team of Montreal, Quebec, Canada

Contents

Project Overview

Quorum-sensing coupled with the Repressilator

Our project is a continuation of one of the projects we presented last year: a two-gene oscillator, with an 'On' switch - LuxI gene, and an 'Off' switch - LacI, expressing a Cyan fluorescent protein when turned on for visualization. This simple relaxation oscillator makes a robust system of oscillations that can act as a 'pace maker' for more complicated oscillating systems. Quorum-sensing coupling between the systems is achieved with a diffusible artificial inducer (AI) protein made from LuxI which couples when produced, to a constitutively expressed gene in the system LuxR which can turn 'on' the system by promoting the synthesis of Lac from pLux. As Lac accumulates, it acts to turn 'off' the system by repressing the pLac controlling the synthesis of LuxI itself. Also, once AI is produced, it can easily diffuse to other cells and continue this 'On'-'Off' oscillator in other neighbouring cells, and hence increasing synchronization across a population of oscillating cells.

This year we've taken this system even further by adding several elements of control to see how they affect oscillations:

  1. Using Lac- Elowitz cells to make cleaner oscillations.
  2. Synthesizing a new I15004 brick to meet our needs.
  3. By changing cell densities and observing their effect on the oscillator.
  4. Adding an AI Analog (AHL) into the system.
  5. Adding Tetracycline (DOX), an inhibitor of the LuxR promoter, to the system and observing its effect.
  6. Adding an AI inhibitor (Aiia) into the system to control the levels of AI produced.
  7. Experimenting with cell divisions through an assay of optical density.


A major enhancement to the system this year is that we plan on actually coupling the Ojalvo, Elowitz et al. - 'Represillator' system to the two-gene oscillator in a single cell. The Repressilator is a 3-gene repressing network, where each gene represses the other, and so on. In turn, this system produces very clear oscillations but is hindered by noise and instability. It is theorized that this system can become highly stabilized if coupled with the 2-gene quorum-sensing oscillator, and once working side-by-side, the 2 systems will produce highly stable, smooth, sinusoidal oscillations.

Fullsystem.jpg

2-genesystem.jpg



Both the quorum-sensing Oscillator and the Repressilator, though observed in a cellular scale in our system, are important in helping understand time-varying conditions in the form of extrinsic driving forces from the environment and intrinsic rhythms generated within an organism itself. This includes specialized rhythm generators functioning in a coherent oscillatory state such as the cardiac pacemaker, also known as the sinoatrial node in mammalian hearts, and the circadian clock residing at the suprachiasmatic nuclei in mammalian brains.

Project Description
How Our System Works
Background Papers


Please feel free to check out our work from last year at iGEM McGill 2006

In the Lab

Lab Notebook
Lab Protocols
Parts/Biobricks
Project Evaluation

The Team

The Team
Mailing List

Pictures

Brown University Meetup (External)
Team Awesome Oscillators