Team:Newcastle/Stochasticity

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===fimE switch===
===fimE switch===

Revision as of 10:38, 22 July 2009


Contents

Stochastic Modelling Tools

Matlab

Matlab can be used for stochastic modelling. Glasgow team used Matlab implementing Gillespie algorithm to incorporate noise among cells. They also used deterministic modelling using ODEs and compared their results. When the number of cells increase two approaches become similar since the noise is cancelled out.

Stocks 2

Stocks 2 is another stochastic simulation tool which also uses Gillespie’s direct method and supports SBML.

Stochastic Switch Examples

Natural switches

Sin (Sporulation Inhibition) operon

Sin (Sporulation Inhibition) operon can be used as the stochastic switch. It is a natural bistable switch.

File:SinOperon.jpg

During normal conditions, SinR is expressed constitutively from P3 and keeps its concentration at a constant level repressing promoter 1. When transcription of promoter1 is activated by phosphorylated Spo0A, both sinI and sinR are expressed from promoter 1. SinI inactivates SinR by forming a complex with sinR upregulating both proteins from promoter1. This cross repression, inhibition of SinR by SinI and the transcriptional represion of sinI by SinR, forms the basis of the bistability. While the positive feedback in the production of SinI enhances the bistability, it also causes increase in sinR levels because of the expression from promoter 1 hence causing oscillations.[1]

Sin operon controls the early stages of sporulation and has a key role to control the sporulation without disturbing its regulation. The threshold of this switch to progress into sporulation can be controlled by varying some parameters, hence providing population heterogeneity. Tight binding of SinR to the first promoter region with fewer sinR molecules increases this heterogeneity. By mutating the first promoter, the binding affinity of sinR the promoter can be increased. With variations on SinI:SinR interaction strength, transcription rate of sinR from the third promoter and the expression rate of SinR, dynamics of the system can be altered.[1]

SinI can be tuned with the paremeters. SinR and SinI can be used to regulate the heavy metal sequestration. Only in a sub population of the bacteria, sinI will be expressed at sufficient levels to trigger our system. Whereas sinR will be expressed in all cells. We can engineer the bacteria so that, when SinI is expressed, it binds to SinR which inhibits heavy metal intake. SinI levels will be sufficient to derepress the intake of heavy metals only in a small population of the cells since it is regulated by spo0A which is active only in a subset of the cells. Spo0A phosplation itself is also a bitsable switch so that a subset of the population will be on spo0A ON state. [2,3] So with this approach we can say that only a small population of the cells will get the heavy metals. If we want the other way we can switch the roles of SinI and sinR.With the normal conditions only 2% of the population express enough sinI.[2]


  1. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1449569
  2. http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=2430929&blobtype=pdf
  3. http://arjournals.annualreviews.org/doi/pdf/10.1146/annurev.micro.62.081307.163002
Sin operon details

Sin operon in GenBank

sinR: Positive regulation of comK; negative regulation of aprE, kinB, sigD, spo0A, spoIIA, spoIIE, spoIIG

http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=NC_000964.2&from=2551885&to=2552220&dopt=gb

sinI:Antagonist of SinR

http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?val=NC_000964.2&from=2551678&to=2551851&dopt=gb

ComK positive autoregulation

fimE switch

  1. fimE switch for DNA re-arrangement

A Tightly Regulated Inducible Expression System Utilising the fim Inversion Recombination Switch.(E. Coli) Timothy S. Ham, Sung Kuk Lee, Jay D. Keasling,Adam P. Arkin,Received 21 December 2005; accepted 2 March 2006 Published online 13 March 2006 in Wiley InterScience (www.interscience.wiley.com). DOI: 10.1002/bit.20916

We could use it switch off or on the production of a protein of our choice, such as the genes involved in germination.

The search for fimE equivalent in Bacillus subtilis

Gene list from BLAST search output in Subtilist web-server (7 matches)

Organism |No. | Gene |Bp | Putative Function | Score | E-value

B.subtilist|BS000101011332|RipX: 295 site specific integrase... 82 | 2.00E-17

B.subtilist|BS000101010965|CodV: 303 sitespecific integrase... 73 | 1.00E-14

B.subtilist|BS000101012099|YdcL: 367 unknown; similar to int... 30 | 0.13

B.subtilist|BS000101011909|AraM: 393 L arabinose operon 27 | 0.64

B.subtilist|BS000101013550|YoeC: 94 unknown; similar to unkn... 25 | 3.2

B.subtilist|BS000101013687|YorC: 125 unknown 24 | 7.1

B.subtilist|BS000101011532|IlvD: 557 dihydroxyacid dehydratase 24 | 7.1

B.subtilist|BS000101010010|YybT: 658 unknown similar to unk... 23 | 9.2


  1. Control of the Arabinose Regulon in Bacillus subtilis by AraR In Vivo: Crucial Roles of Operators, Cooperativity, and DNA Looping
  2. Binding of the Bacillus subtilis spoIVCA product to the recombination sites of the element interrupting the sigma K-encoding gene =>...DNA rearrangement that depends on the spoIVCA gene product...

Hin/Hix system

In 2006, Davidson team tried to solve the burnt pancake problem by using DNA rearrangement using Hin/Hix system from Salmonella typhimurium. (http://parts2.mit.edu/wiki/index.php/Davidson_2006.) Basically they tried to use the bacteria as a biomemory! They also have a paper published which is attached.

Their animation explains the process quite well. (http://www.bio.davidson.edu/people/kahaynes/FAMU_talk/Living_computer.swf)

The parts they submitted to the parts registry have "W" flag which means they are working. http://partsregistry.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2006&group=iGEM2006_Davidson




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