Team:Cambridge/Signalling
From 2008.igem.org
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=Introduction= | =Introduction= | ||
- | We | + | We designed a simple two-component Reaction-Diffusion system in the gram-positive model organism [[Team:Cambridge/Bacillus | ''Bacillus subtilis'']]. In 1952, Alan Turing famously described this system and suggested it as the basis for self-organization and pattern formation in biological systems. The simplest of these patterns, which we are planning to model in bacteria, mimic the spots and stripes seen on animal coats. |
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<center>http://www.uni-muenster.de/Physik.AP/Purwins/RD/2kgl.gif</center> | <center>http://www.uni-muenster.de/Physik.AP/Purwins/RD/2kgl.gif</center> | ||
#http://www.uni-muenster.de/Physik.AP/Purwins/RD/struktur-e.gif | #http://www.uni-muenster.de/Physik.AP/Purwins/RD/struktur-e.gif | ||
- | #http://www.rsc.org/ej/MB/2007/b701571b/b701571b-f1.gif | + | #http://www.rsc.org/ej/MB/2007/b701571b/b701571b-f1.gif |
(A) The model consists of two diffusible signals secreted by every cell. The activator, which is controlled by a stochastic bistable switch, turns on itself and its own inhibitor. (B) A field of cells can be stably patterned into two different zones, so long as the inhibitor diffuses faster than the activator. The activator and inhibitor are synthesized in the source at the center, and turned off by accumulation of the inhibitor in the periphery. | (A) The model consists of two diffusible signals secreted by every cell. The activator, which is controlled by a stochastic bistable switch, turns on itself and its own inhibitor. (B) A field of cells can be stably patterned into two different zones, so long as the inhibitor diffuses faster than the activator. The activator and inhibitor are synthesized in the source at the center, and turned off by accumulation of the inhibitor in the periphery. | ||
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http://parts.mit.edu/igem07/images/3/32/Cambridge_Agr_operon_and_biochemical_pathways.png | http://parts.mit.edu/igem07/images/3/32/Cambridge_Agr_operon_and_biochemical_pathways.png | ||
- | + | Our system uses two well-characterized bacterial communication systems to generate this behavior. The agr peptide signalling system from S. aureus serves as our activatory signal (pictured), while the lux system from V. fischeri serves as our inhibitor. Bacillus subtilis serves as an excellent chassis for this project because of the ease with which chromosomal integration can be performed. This project will focus on a tight integration of modeling and experiment; we will test different promoter strengths and other variables, feed these system parameters into our multi-cell models, and then use those models to tweak the regulatory machinery that will control signal production. | |
==Grasshopper Example== | ==Grasshopper Example== | ||
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=Objective= | =Objective= | ||
[[image:igem-whiteboard.jpg|thumb|right|Schematic of Activator/Inhibitor system in B. subtilis]] | [[image:igem-whiteboard.jpg|thumb|right|Schematic of Activator/Inhibitor system in B. subtilis]] | ||
- | This project seeks to generate [[Wikipedia:Turing Patterns|Turing Patterns]] by creating a [[Wikipedia:Reaction-Diffusion System|Reaction-Diffusion system]] in the [[Wikipedia:gram-positive bacteria|gram-positive bacteria]] [[Wikipedia:Bacillus subtilis|Bacillus subtilis]]. | + | This sub-project seeks to generate [[Wikipedia:Turing Patterns|Turing Patterns]] by creating a [[Wikipedia:Reaction-Diffusion System|Reaction-Diffusion system]] in the [[Wikipedia:gram-positive bacteria|gram-positive bacteria]] [[Wikipedia:Bacillus subtilis|Bacillus subtilis]]. Our goal was to integrate two signalling systems into this bacterium and use an autofeedback mechanism to generate self-organizing patterns from random noise. We planned to incorporate the ''agr'' peptide signalling system from ''S. aureus'' and the ''lux'' AHL system from ''V. fisheri''. |
== Materials == | == Materials == | ||
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=== [[Team:Cambridge/Signalling/Vectors | Vectors]] === | === [[Team:Cambridge/Signalling/Vectors | Vectors]] === | ||
- | * | + | * Details of vectors we used, including maps, sequences, and testing |
=== [[Team:Cambridge/Signalling/Primers | Primers]] === | === [[Team:Cambridge/Signalling/Primers | Primers]] === | ||
- | * | + | * List of primers we have ordered |
=== [[Team:Cambridge/Signalling/Constructs | Constructs]] === | === [[Team:Cambridge/Signalling/Constructs | Constructs]] === | ||
- | * | + | * Planning and organization of biobrick assemblies and recombinant plasmids |
- | == [[Team:Cambridge/ | + | === [[Team:Cambridge/Signalling/Lab Work| Lab Work Page]] === |
+ | * Main page detailing our day-to-day research activities | ||
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- | + | === [[Team:Cambridge/Signalling/Experiments| Experiments]] === | |
+ | * Main page detailing our planned and completed experiments | ||
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Revision as of 03:13, 30 October 2008
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IntroductionWe designed a simple two-component Reaction-Diffusion system in the gram-positive model organism Bacillus subtilis. In 1952, Alan Turing famously described this system and suggested it as the basis for self-organization and pattern formation in biological systems. The simplest of these patterns, which we are planning to model in bacteria, mimic the spots and stripes seen on animal coats.
(A) The model consists of two diffusible signals secreted by every cell. The activator, which is controlled by a stochastic bistable switch, turns on itself and its own inhibitor. (B) A field of cells can be stably patterned into two different zones, so long as the inhibitor diffuses faster than the activator. The activator and inhibitor are synthesized in the source at the center, and turned off by accumulation of the inhibitor in the periphery. http://parts.mit.edu/igem07/images/3/32/Cambridge_Agr_operon_and_biochemical_pathways.png Our system uses two well-characterized bacterial communication systems to generate this behavior. The agr peptide signalling system from S. aureus serves as our activatory signal (pictured), while the lux system from V. fischeri serves as our inhibitor. Bacillus subtilis serves as an excellent chassis for this project because of the ease with which chromosomal integration can be performed. This project will focus on a tight integration of modeling and experiment; we will test different promoter strengths and other variables, feed these system parameters into our multi-cell models, and then use those models to tweak the regulatory machinery that will control signal production. Grasshopper ExampleThe reaction-diffusion system depends on an activator and inhibitory signal that spread throughout the medium. The "grasshopper" example is quite intuitive: Imagine it is hot and there is a field of dry grass with grasshoppers. Suddenly, a fire starts burning at some point and spreads (the activator signal) so that the grasshoppers move away from that point to avoid the fire. However, the grasshoppers also generate moisture (the inhibitory signal) thus preventing the areas of dry grass the grasshoppers move to of catching fire. The initial patch will have burnt down. However, the surrounded area will be saturated by moisture generated by the grasshoppers thus preventing the fire from spreading. Imagine now that at the beginning, not a single patch, but numerous randomly distributed patches (resembling noise) of dry grass catch fire. The resulting patterning of charred grass and grasshoppers is called a Turing Pattern. It is important to note that the inhibitory signal (grasshoppers) must travel faster than the activation signal (fire) as to prevent the whole field from burning down which would result in no patterning at all. ObjectiveThis sub-project seeks to generate Turing Patterns by creating a Reaction-Diffusion system in the gram-positive bacteria Bacillus subtilis. Our goal was to integrate two signalling systems into this bacterium and use an autofeedback mechanism to generate self-organizing patterns from random noise. We planned to incorporate the agr peptide signalling system from S. aureus and the lux AHL system from V. fisheri. MaterialsBacillus StrainsBacillus strain 1A1 (derivative of standard strain 168)
Bacillus strain 1A771 (derivative of standard strain 168)
Bacillus strain 1A751 (derivative of standard strain 168)
Vectors
Primers
Constructs
Lab Work Page
Experiments
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