Cambridge University 2006
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Position dependent gene expression is a critical aspect of the behaviour of multi-cellular organisms and requires a complex series of interactions to occur between cell types. Cells adopt a particular fate in response to a combination of chemical signals. The development of body axes in multi-cellular organisms is a case in point illustrating the importance of cellular communication for developing complex patterns. <br> | Position dependent gene expression is a critical aspect of the behaviour of multi-cellular organisms and requires a complex series of interactions to occur between cell types. Cells adopt a particular fate in response to a combination of chemical signals. The development of body axes in multi-cellular organisms is a case in point illustrating the importance of cellular communication for developing complex patterns. <br> | ||
We used Escherichia coli as the organism of choice for our experiments and observed how differential cell motility can in itself lead to complex pattern formation (Figure 1???). | We used Escherichia coli as the organism of choice for our experiments and observed how differential cell motility can in itself lead to complex pattern formation (Figure 1???). | ||
| - | Transforming E. coli strains with fluorescent proteins allowed us to observe more vivid patterns (Figure 2???). | + | Transforming E. coli strains with fluorescent proteins allowed us to observe more vivid patterns (Figure 2???). We genetically engineered an E. coli cell population to render it capable of producing an acyl-homoserine lactone signal (sender cells). We verified that the cells were producing lactones using the CVO26 plate assay described by McClean et al. (Figure 3???). A second E. coli population was rendered capable of responding to this acyl homoserine lactone signal(receiver cells). Adapting the experiments of Weiss et al., using cell motility, rather than a differential response to AHL concentrations as a way to define zones of response we noted how the interaction of sender and receiver cell populations on a swimming plate leads to complex pattern formation (Figure 2???). <br> |
| - | We genetically engineered an E. coli cell population to render it capable of producing an acyl-homoserine lactone signal (sender cells). We verified that the cells were producing lactones using the CVO26 plate assay described by McClean et al. (Figure 3???). | + | |
| - | A second E. coli population was rendered capable of responding to this acyl homoserine lactone signal(receiver cells). Adapting the experiments of Weiss et al., using cell motility, rather than a differential response to AHL concentrations as a way to define zones of response we noted how the interaction of sender and receiver cell populations on a swimming plate leads to complex pattern formation (Figure 2???). <br> | + | |
For both experiments mentioned above we used parts from the MIT Registry of Standard Biological Parts, thus characterizing their function in this novel fashion. Thereafter, we proceeded to make the genetic constructs described in “Biological Parts” below. Equipping highly motile strains such as E. coli MC1000 with AHL-mediated autoinducing systems based on Vibrio fischeri luxI/luxR and Pseudomonas aeruginosa lasI/lasR cassettes would allow the amplification of a response to an AHL signal and its propagation. Exploiting the uncoupled nature of sender and receiver entities, both AHL systems can be combined to give two-way communication pathways. The recursive behaviour of cells being both sender and receiver at the same time has the potential to create patterns that are robust and more complex in nature. In order to allow a detailed study of ensuing interactions at microscopic and macroscopic levels, two populations of E. coli can be endowed with the genetic circuits necessary for this reciprocal behaviour. These genetic circuits are described in “Biological Parts” below. <br> | For both experiments mentioned above we used parts from the MIT Registry of Standard Biological Parts, thus characterizing their function in this novel fashion. Thereafter, we proceeded to make the genetic constructs described in “Biological Parts” below. Equipping highly motile strains such as E. coli MC1000 with AHL-mediated autoinducing systems based on Vibrio fischeri luxI/luxR and Pseudomonas aeruginosa lasI/lasR cassettes would allow the amplification of a response to an AHL signal and its propagation. Exploiting the uncoupled nature of sender and receiver entities, both AHL systems can be combined to give two-way communication pathways. The recursive behaviour of cells being both sender and receiver at the same time has the potential to create patterns that are robust and more complex in nature. In order to allow a detailed study of ensuing interactions at microscopic and macroscopic levels, two populations of E. coli can be endowed with the genetic circuits necessary for this reciprocal behaviour. These genetic circuits are described in “Biological Parts” below. <br> | ||
| - | Although we were unable to construct the complete system described below, we were able to construct auto-inducing luxI/R and lasI/R cassettes | + | Although we were unable to construct the complete system described below, we were able to construct auto-inducing luxI/R and lasI/R cassettes. We were also able to model the behaviour of cells within populations containing these systems. Further, we believe that in the future it may be possible to equip E. coli populations with more complex genetic circuits that would allow two interspersed subpopulations of isogenic bacteria to battle for dominance on a swimming plate. They would initially be either red or green; on encountering each other in sufficient numbers, defeated bacteria would defect to the opposing side by a switch mechanism. They would change colour and start producing a new battle signal to command the fight under the opposite banner. This is described in detail in “Future Directions”.(We have submitted some parts to the Registry that would make easier the engineering of these complex genetic circuits and the construction of such a population based bi-stable switch a more realistic goal). <br> |
| - | Further, we believe that in the future it may be possible to equip E. coli populations with more complex genetic circuits that would allow two interspersed subpopulations of isogenic bacteria to battle for dominance on a swimming plate. They would initially be either red or green; on encountering each other in sufficient numbers, defeated bacteria would defect to the opposing side by a switch mechanism. They would change colour and start producing a new battle signal to command the fight under the opposite banner. This is described in detail in “Future Directions”.(We have submitted some parts to the Registry that would make easier the engineering of these complex genetic circuits and the construction of such a population based bi-stable switch a more realistic goal). <br> | + | |
For some of our constructions we used the method of 3-Antibiotic assembly, described by Tom Knight et al. We were able to purify standard plasmid backbone vectors for this assembly method and also to get it to work for some of the constructions as evidenced by the parts submitted. <br> | For some of our constructions we used the method of 3-Antibiotic assembly, described by Tom Knight et al. We were able to purify standard plasmid backbone vectors for this assembly method and also to get it to work for some of the constructions as evidenced by the parts submitted. <br> | ||
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Revision as of 16:12, 21 October 2006
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| - Autonomous Pattern Formation between Bacterial Populations by Reciprocal Communication - |
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Project Summary
Our entry for the iGEM 2006 competition sought to genetically engineer two types of bacteria such that they would autonomously form patterns in swimming agar. We studied the dynamics of pattern formation between bacterial populations. In particular, we investigated the interaction of genetically engineered E. coli sender cells, producing an acyl homoserine lactone signal, and receiver cells in swimming agar. We then attempted to render these cells capable of reciprocal communication and sought to construct biological parts that would render possible the construction of a population based bi-stable switch. Furthermore, we modelled the behaviour of single cells as well as the interactive behaviour of populations of cells containing these genetic circuits. Our experiments verified that differential cell motility in combination with position-dependent gene expression has the potential to generate complex patterns.
Introduction
Position dependent gene expression is a critical aspect of the behaviour of multi-cellular organisms and requires a complex series of interactions to occur between cell types. Cells adopt a particular fate in response to a combination of chemical signals. The development of body axes in multi-cellular organisms is a case in point illustrating the importance of cellular communication for developing complex patterns.
We used Escherichia coli as the organism of choice for our experiments and observed how differential cell motility can in itself lead to complex pattern formation (Figure 1???). Transforming E. coli strains with fluorescent proteins allowed us to observe more vivid patterns (Figure 2???). We genetically engineered an E. coli cell population to render it capable of producing an acyl-homoserine lactone signal (sender cells). We verified that the cells were producing lactones using the CVO26 plate assay described by McClean et al. (Figure 3???). A second E. coli population was rendered capable of responding to this acyl homoserine lactone signal(receiver cells). Adapting the experiments of Weiss et al., using cell motility, rather than a differential response to AHL concentrations as a way to define zones of response we noted how the interaction of sender and receiver cell populations on a swimming plate leads to complex pattern formation (Figure 2???).
For both experiments mentioned above we used parts from the MIT Registry of Standard Biological Parts, thus characterizing their function in this novel fashion. Thereafter, we proceeded to make the genetic constructs described in “Biological Parts” below. Equipping highly motile strains such as E. coli MC1000 with AHL-mediated autoinducing systems based on Vibrio fischeri luxI/luxR and Pseudomonas aeruginosa lasI/lasR cassettes would allow the amplification of a response to an AHL signal and its propagation. Exploiting the uncoupled nature of sender and receiver entities, both AHL systems can be combined to give two-way communication pathways. The recursive behaviour of cells being both sender and receiver at the same time has the potential to create patterns that are robust and more complex in nature. In order to allow a detailed study of ensuing interactions at microscopic and macroscopic levels, two populations of E. coli can be endowed with the genetic circuits necessary for this reciprocal behaviour. These genetic circuits are described in “Biological Parts” below.
Although we were unable to construct the complete system described below, we were able to construct auto-inducing luxI/R and lasI/R cassettes. We were also able to model the behaviour of cells within populations containing these systems. Further, we believe that in the future it may be possible to equip E. coli populations with more complex genetic circuits that would allow two interspersed subpopulations of isogenic bacteria to battle for dominance on a swimming plate. They would initially be either red or green; on encountering each other in sufficient numbers, defeated bacteria would defect to the opposing side by a switch mechanism. They would change colour and start producing a new battle signal to command the fight under the opposite banner. This is described in detail in “Future Directions”.(We have submitted some parts to the Registry that would make easier the engineering of these complex genetic circuits and the construction of such a population based bi-stable switch a more realistic goal).
For some of our constructions we used the method of 3-Antibiotic assembly, described by Tom Knight et al. We were able to purify standard plasmid backbone vectors for this assembly method and also to get it to work for some of the constructions as evidenced by the parts submitted.
