Team:LCG-UNAM-Mexico:WTM

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* <h2>Insertion and translocation of T7 DNA at different times</h2>
* <h2>Insertion and translocation of T7 DNA at different times</h2>
<br>Entry of T7 DNA into the host cell occurs in several distinct stages.
<br>Entry of T7 DNA into the host cell occurs in several distinct stages.
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<br>Phage's DNA is arranged in three classes of genes depending on their positions, it is translocated into the cell between 6 to 10 minutes after attachment, so this order and timing drives the phage's development. This phenomenon of DNA translocation is modeled here taking into account reported insertion speeds [REFERENCE].  
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<br>Phage's DNA is arranged in three classes of genes depending on their positions, it is translocated into the cell between 6 to 10 minutes after attachment, so this order and timing drives the phage's development. This phenomenon of DNA translocation is modeled here taking into account reported insertion speeds F. Buchholtz et al. 1987[1].  
* <h2>Transcription of different T7 DNA segments into polycistronic mRNAs</h2>
* <h2>Transcription of different T7 DNA segments into polycistronic mRNAs</h2>
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* <h2>Degradation of phage mRNAs</h2>
* <h2>Degradation of phage mRNAs</h2>
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<br>We assume the same degradation rate for all T7 polycistronic mRNAs. Until now impact of this phenomenon had not been studied. It has been found that phage messengers are stabler than Bacterial mRNAs [REFERENCE].   
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<br>We assume the same degradation rate for all T7 polycistronic mRNAs. Until now impact of this phenomenon had not been studied. It has been found that phage messengers are stabler than Bacterial mRNAs .Yoshihiko Yamada et al 1975 [2].   
* <h2>Translation of phage mRNAs into proteins</h2>
* <h2>Translation of phage mRNAs into proteins</h2>
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* <h2>Procapsid Assembly</h2>
* <h2>Procapsid Assembly</h2>
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<br>This phenomenon is simulated in almost the same way as Drew Endy et al. 1996 using mass action kinetics.  
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<br>This phenomenon is simulated in almost the same way as Drew Endy et al. 1996 [3] using mass action kinetics.  
* <h2>DNA packaging and final assembly</h2>
* <h2>DNA packaging and final assembly</h2>
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<h2>References</h2>
<h2>References</h2>
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<br>[1] F. Buchholtz and F.W. Schneider. 1987. '''Computer simulation of T3/T7 phage infection using lag times''' 
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<br>[2] Yoshihiko Yamada, Patricia A. Whitaker and Dai Nakada. 1975. '''Chemical Stability of Bacteriophage T7 Early mRNA'''
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<br>[3] Drew Endy, Deyu Kong, John Yin. 1996. '''Intracellular Kinetics of a Growing Virus: A Genetically Structured Simulation for Bacteriophage T7'''
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Latest revision as of 01:08, 22 October 2009

WILD-TYPE MOLECULAR MODEL (WTM)

WTM Simbiology ® diagram

WTM is a stochastic molecular model of bacteriophage T7 life cycle, it was constructed to simulate wild-type development of this phage in E Coli.
Both models, WTM and KZM, were constructed to monitor the evolution and abundance of molecular species in the systems. For the purpose of this project we are particularly concerned in the abundance of phage T7 (burst size) at the end of the cycle (720 seconds) in each infection event.
Ensembles of runs of WTM and KZM will provide us with data to build Burst Size Distributions for each model. BSDs are next utilized by the population models to recreate the impact of phage infections at the population level.

See also KZM, BSD, Population Model, Cellular Automata.

Contents

The following critical processes are accounted in this model:

  • Insertion and translocation of T7 DNA at different times


Entry of T7 DNA into the host cell occurs in several distinct stages.
Phage's DNA is arranged in three classes of genes depending on their positions, it is translocated into the cell between 6 to 10 minutes after attachment, so this order and timing drives the phage's development. This phenomenon of DNA translocation is modeled here taking into account reported insertion speeds F. Buchholtz et al. 1987[1].

  • Transcription of different T7 DNA segments into polycistronic mRNAs


It has been shown that T7 genes are expressed in overlapped polycistronic mRNAs.
Transcription of T7 polycistronic mRNAs occurs if and only if its coding DNA segment is available in the cell. Transcription is dependent of the set of genes inserted at a time.
We define a set of transcription rates for every polycistronic mRNA taking into account constant bacterial or T7 RNA polymerase elongation rates and the length of the polycistronic mRNA, these transcription rates will be our rate limiting steps at the transcriptional level.

  • Degradation of phage mRNAs


We assume the same degradation rate for all T7 polycistronic mRNAs. Until now impact of this phenomenon had not been studied. It has been found that phage messengers are stabler than Bacterial mRNAs .Yoshihiko Yamada et al 1975 [2].

  • Translation of phage mRNAs into proteins


In this model, translation is simulated assuming an environment of unlimited amino acids and ribosomes. We also assume that the rate at which ribosomes incorporate amino acids is constant over all T7 mRNA.
As it has been done for transcription we define a set of translation rates for every protein taking into account a constant ribosome elongation rate and the length of the protein, these translation rates will be our rate limiting steps at the translational level.

  • T7 DNA replication


DNA synthesis is simulated by taking elongation of T7 DNA polymerase as the rate-limiting step.
We assume an environment of limited free nucleotides so we can set a maximum number of T7 genomes produced in a single infection taking into account the size of the host genome (and this includes bacterial chromosomes, plasmids and other sources of free nucleotides).

  • Procapsid Assembly


This phenomenon is simulated in almost the same way as Drew Endy et al. 1996 [3] using mass action kinetics.

  • DNA packaging and final assembly


Both processes are modeled using mass action kinetics as well. This last step requires complete procapsids, T7 DNA, and enough of each structural protein to complete the phage. The simulation assumes that packaging of DNA into the procapsid is the rate-limiting step for T7 progeny formation.

  • Simulation, performance and BSD construction


The next video has been recorded from a single simulation of WTM, with this algorithm we can monitor the evolution and abundance of molecular species in time.


For the purpose of our project we're just concerned in the burst size an infected cell could produce in each infection process, as we said above BSDs for WTM and KZM can be assembled with many runs of each model so we can compare the performance of our synthetic kamikaze and the wild-type systems at molecular and population levels.
Generated BSDs are next used by Cellular Automaton to choose the burst size an infected cell (with and without our kamikaze system) is going to release into the medium.
BSDs are also use by the agent-based model, in both cases BZDs drives the fate of the population.

In this video there are two molecular species plotted, ABproteins or Major head proteins, this protein is the main component of T7 procapsids, it is evident the upper limit of molecules at which a procapsid assembly occurs. Production of this protein grows faster at late stages when polycistronic mRNAs responsible for them become more and more abundant in the cell. T7 plotted in red grows until it reach a burst size of about 250 phages at the end of the cycle/simulation (lysis time 720 seconds).

References


[1] F. Buchholtz and F.W. Schneider. 1987. Computer simulation of T3/T7 phage infection using lag times
[2] Yoshihiko Yamada, Patricia A. Whitaker and Dai Nakada. 1975. Chemical Stability of Bacteriophage T7 Early mRNA
[3] Drew Endy, Deyu Kong, John Yin. 1996. Intracellular Kinetics of a Growing Virus: A Genetically Structured Simulation for Bacteriophage T7


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