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Turing meets synthetic biology

Introduction

The work of Turing

In 1952 Alan M. Turing in his classical paper called The chemical basis of morphogenesis he sugested that "...a system of chemical substances, called morphogens, reacting together and diffusing through a tissue, is adequate to account for the main phenomena of morphogenesis." This system is amazing by its simplicity. With only two morphogens it's possible to reproduce nontrivial patterns that are similar to those of zebras or leopards.

Although there is not enough evidence of the existence of these morphogens in living organisms, the likeliness of the patterns obtained by theoretical means using this model with the ones found in nature is astonishing.

Turing assumed that the morphogenes can react with each other and diffuse through cells. It is necessary that at the beginning there is a non-homogeneous distribuition of these morphogenes, which is often called chemical prepattern and can be given merely by random disturbances. An intuitive notion would tell us that the diffusion of the morphogenes starting from this chemical prepattern would led to a homogenous state of the system, but surprisingly the Turing proposal says that non-homgenous structures will arise, as a direct consequence of diffusion (the turing hyphotesis); reaching a stable state with regions with high concentrantions of one morphogen and regions with high concentration of the others. This non-homogeneous distribuition patterns of morphogens resembles those found in nature during some stages of morhpogenesis (from the gastrulation or the tentacle patterns on hydras to the jaguar spots).

Reaction-Diffusion equations

Turing formally described his proposal with a set of Partial Differential Equations where is possible to represent the chemical interactions of the morphogens and the way they move over the space. This kind of dynamics are commonly called reaction-diffusion mechanisms, and the equations that describe them are named Reaction-Diffusion equations. In section modeling we formally present them.

The Activator-Inhibitor

In 1972 A. Gierer and H. Meinhardt published his work called A theory of biological pattern formation presenting a network based in the interaction of at least two morphogenes acting as an activator and an inhibitor. The main qualitative dynamics of the morphogens is:

Short range activation, longer range inhibition and a conceptual distinction between effective concentrations of activator and inhibitor, on one hand, and the density of their sources on the other.

Schematically we can see this description as:

IMAGEN

J.D. Murray presented a good example of how patterns can arise from this kind of dynamics so we cite his text literally:

Consider a field of dry grass in which there is a large number of grasshoppers which can generate a lot of moisture by sweating if they get warm. Now suppose the grass is set alight at some point and a flame front starts to propagate. We can think of the grasshopper as an inhibitor and the fire as an activator. If there were no moisture to quench the flames the fire would simply spread over the whole field which would result in a uniform charred area. Suppose, however, that when the grasshoppers get warm enough they can generate enough moisture to dampen the grass so that when the flames reach such a pre-moistened area the grass will not burn. The scenario for spatial pattern is then as follows. The fire starts to spread it is one of the reactants, the activator, with a diffusion coefficient DF say. When the grasshoppers, the inhibitor reactant, ahead of the flame front feel it coming they move quickly well ahead of it; that is, they have a diffusion coefficient, DG say, which is much larger than DF . The grasshoppers then sweat profusely and generate enough moisture to prevent the fire spreading into the moistened area. In this way the charred area is restricted to a finite domain which depends on the diffusion coefficients of the reactants fire and grasshopperand various reaction parameters. If, instead of a single initial fire, there were a random scattering of them we can see how this process would result in a final spatially heterogeneous steady state distribution of charred and uncharred regions in the field and a spatial distribution of grasshoppers, since around each fire the above scenario would take place. If the grasshoppers and flame front diffused at the same speed no such spatial pattern could evolve.

Synthesizing, we can now represent the interactions between the activator and the inhibitor as follows:

The activator is autocathalyzed and it also triggers the formation of the inhibitor. Accordingly to its name, the inhibitor inhibits the production of the activator, leading to a simple but very rich dymamics (For more details on the acivator-inhibitor equations please go to modelling section). From the grass field and the fire analogy we can deduce that the diffusion coefficients of the fire should be slower than the grasshoppers one; if not the fire (activator) would spread completely in the area. This is an important fact that we mention again later.

GENERAL CONDITIONS FOR PATTERN GENERATION

Although this kind of conditions refers mainly to a mathematical analyses of the reaction-diffusion systems like the Activator-Inhibitor of J.D. Murray , we can qualitative simplify and establish according to this analyses the general conditions for pattern formation:

The existence of at least of two morphogenes with different nature that interacts chemically between them diffuse over the space
The coefficient rates of diffusion should be different.
The starting distribution of morphogenes should not be completely homogeneous over the space.
The Gierer and Mainhardt proposal: local activation and longe range inhibition.

TURING MEETS SYNTHETIC BIOLOGY

The Synthetic Biology has become in the last years an excellent tool to designe biological systems with particular purposes. In our team we decided to used it as a way to contribute not only with technological aspects but mainly with theoretical and foundational research.

The Turing's ideas about cellular differentiation in zygote according to gradients of morphogenes that react and diffuse through the cellular tissue have not been completely confirmed due to the lack of biological evidence. The main objective of this project is to give an example of a biological system that contains reaction-diffusion mechanisms and is able to reproduce spatiotemporal Turing-type patterns or another kind of nontrivial patterns.

The biobricks found in the [http://www.partsregistry.org Registry of Biological parts] are a good starting point to construct a synthetic network of genes that due to their interactions could be identified as an Activator-Inhibitor system. This genetic network inserted innto an E. coli' should respond to the concentration gradient of morphogens in the media and have the potential to differentiate accordingly.

The main challenge was to design a synthetic network that fulfill the general conditions for generating a spatiotemporal pattern (see above). But we must act carefully, since in Murray's book says literaly:

"...the genes, however, themselves cannot create the pattern. They only provide a blueprint or recipe, for the pattern generation"

an advise that few teams in the past years' competitions may have considered considered.

Morphogenesis qualitative mechanisms

Reaction-Diffusion systems implemented on Biobricks

Inspired by the Gierer and Mainhardt work we designed a synthetic genetic network that acts as an Activator-Inhibitor with limiting substrates. We explain each particular characteristics of reaction, diffusion and substrates in the following subsections.

Reaction - Diffusion

We suppose the existence of two morphogenes, represented by Lux and Las , AI and PAI lactones respectively. This substances are very small and travel throw the membrane, and diffuse fast in the media.

We used two promoters, one inducible by LasR+PAI ([http://www.partsregistry.org/Part:Bba_R0079 Bba_R0079]) and the other double controlled ([http://www.partsregistry.org/Part:Bba_RK091146 Bba_K091146]), repressed by LuxR+AI and induced by LasR+PAI; in our genetic network we gave the cell the posibility of responde to a gradient of PAI and AI and express GFP.

We used too a constitutive Lac Inverter, to control the production of LasR with IPTG, a constitutive Tet inverter that controls LuxR with ATC. These inverters provides a good way to control the systems and make it more sensitive for parameters adjust.

For a complete description of the biobricks check parts section.

Lac inverter

Tet inverter

Lux AHL

Las AHL

Substrates

[http://openwetware.org/wiki/IPTG IPTG] & [http://openwetware.org/wiki/ATc ATC]

@@ Line 123: / Line 123: @@
 ===Reaction - Diffusion===
+We suppose the existence of two morphogenes, represented by ''Lux'' and ''Las'' , ''AI'' and ''PAI'' lactones respectively. This substances are very small and travel throw the membrane, and diffuse fast in the media.
-We suppose the existence of two morphogenes, represented by Lux and Las , AI and PAI lactones  respectively. This substances are very small and travel throw the membrane, and diffuse fast in the media.
+We used two promoters, one inducible by ''LasR''+''PAI'' ([http://www.partsregistry.org/Part:Bba_R0079 Bba_R0079]) and the other double controlled ([http://www.partsregistry.org/Part:Bba_RK091146 Bba_K091146]), repressed by ''LuxR''+''AI ''and induced by ''LasR''+''PAI''<nowiki>; in our genetic network we gave the cell the posibility of responde to a gradient of </nowiki>''PAI'' and ''AI ''and express ''GFP''.
-We used two promoters, one inducible by LasR+PAI (BBa_R0079) and the other double controlled (BBa_K091146),  repressed by LuxR+AI  and induced by LasR+PAI; in our genetic network to give the cell the posibility of responde to a gradient of PAI and AI.
+We used too a constitutive ''Lac'' Inverter, to control the production of ''LasR'' with ''IPTG'', a constitutive ''Tet'' inverter that controls ''LuxR'' with ''ATC. ''These inverters provides a good way to control the systems and make it more sensitive for parameters adjust.
-===Reaction===
+For a complete description of the biobricks check [[Team:IPN-UNAM-Mexico/Parts | parts section]].
 '''[[Team:IPN-UNAM-Mexico/Parts | Lac inverter]]'''
@@ Line 140: / Line 142: @@
 [[Image:AI Tet.jpg‎‎‎|500px|center|link=https://2009.igem.org/Team:IPN-UNAM-Mexico/Parts]]
-===Diffusion===
 '''[[Team:IPN-UNAM-Mexico/Parts | Lux AHL]]'''
@@ Line 150: / Line 150: @@
 [[Image:AI LasI.jpg‎‎‎|400px|center|Las AHL]]

Team:IPN-UNAM-Mexico/Project

From 2009.igem.org

Revision as of 20:24, 21 October 2009

Turing meets synthetic biology

Introduction

The work of Turing

Reaction-Diffusion equations

The Activator-Inhibitor

GENERAL CONDITIONS FOR PATTERN GENERATION

TURING MEETS SYNTHETIC BIOLOGY

Morphogenesis qualitative mechanisms

Reaction-Diffusion systems implemented on Biobricks

Reaction - Diffusion

Substrates

The Activator-Inhibitor system on biobricks: The dynamics

Autocatalisis

Activation

Inhibition

Diffusion

Substrates

Complete system