Team:DTU-Denmark/Vision

From 2011.igem.org

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== The idea ==
== The idea ==
[[File:swiss_army_knife.jpg|400px|thumb|right|middle|]]
[[File:swiss_army_knife.jpg|400px|thumb|right|middle|]]
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The chitobiose system in ''E. coli'' is regulated in a highly interesting way: A small RNA regulates the expression in a manner that is conceptually similar to the highly versatile miRNAs of Eukaryotes. The RNA selectively targets and facilitates the degradation of the mRNA of its target gene. The region used for targeting is easily identified upon inspection of the small RNA sequence, as it is highly similar to the targeted Shine-Dalgarno.
 
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We believe it is possible use this system as an engineering framework for trans-acting RNA regulation. Since previous work on small RNAs in bacteria show that it is possible control the target of a small RNA by changing its sequence ???CITE???, this system could act as a universal tool for easy and specific gene silencing, both outside and within the Biobrick standard.
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We believe it is possible use a system found in ''E. coli'', namely the chitobiose system, as an engineering framework for trans-acting RNA regulation. Since previous work on small RNAs in bacteria show that it is possible control the target of a small RNA by changing its sequence ???CITE???, this system could act as a universal tool for easy and specific gene silencing, both outside and within the Biobrick standard.
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The chitobiose system in ''E. coli'' is regulated in a highly interesting way: A small RNA regulates the expression in a manner that is conceptually similar to the highly versatile miRNAs of Eukaryotes. The RNA selectively targets and facilitates the degradation of the mRNA of its target gene. The region used for targeting is easily identified upon inspection of the small RNA sequence, as it is highly similar to the targeted Shine-Dalgarno.
As an added bonus this system would work in addition to any previously employed promoter based regulation, and due to the existence of a second small RNA to regulate the first, highly advanced schemes of regulation such as pulses can be achieved.
As an added bonus this system would work in addition to any previously employed promoter based regulation, and due to the existence of a second small RNA to regulate the first, highly advanced schemes of regulation such as pulses can be achieved.

Revision as of 13:44, 20 September 2011

Vision

Contents

The idea

Swiss army knife.jpg

We believe it is possible use a system found in E. coli, namely the chitobiose system, as an engineering framework for trans-acting RNA regulation. Since previous work on small RNAs in bacteria show that it is possible control the target of a small RNA by changing its sequence ???CITE???, this system could act as a universal tool for easy and specific gene silencing, both outside and within the Biobrick standard.

The chitobiose system in E. coli is regulated in a highly interesting way: A small RNA regulates the expression in a manner that is conceptually similar to the highly versatile miRNAs of Eukaryotes. The RNA selectively targets and facilitates the degradation of the mRNA of its target gene. The region used for targeting is easily identified upon inspection of the small RNA sequence, as it is highly similar to the targeted Shine-Dalgarno.

As an added bonus this system would work in addition to any previously employed promoter based regulation, and due to the existence of a second small RNA to regulate the first, highly advanced schemes of regulation such as pulses can be achieved.

In short we believe this to be a "Swiss army knife" of gene silencing.

The advantages

There are many reasons for using our system instead of, or in addition to, the more commonly used solutions. Here are a few:

The biggest reason is ease of use: Design the system in silico, order it and transform it. Done... You have now knocked down a gene. Since the small RNA, as indicated by the name, is small this is not a big expense.

The second big reason is area of applicability. Any organism that is:

  • Sequenced
  • Has known stable plasmids
  • Has hfq
  • Is transformable

Is a potential target for our system. This includes many organisms that are difficult or impossible to chromosomally engineer.

For the scientists there are a few more advantages: You can easily knock down genes in the middle of a gene,

The problem(s) we solve

But why would one even want a transacting RNA system for regulating gene expression?

Apart from being easy to use, it lets you


The trap-RNA system can target any gene

The trap-RNA system provides unique flexibility for gene silencing in prokaryotes enabling control and tuning of gene expression. The specificity of the system depends on base pair complementarity. Therefore it can be designed to target any gene of interest by simply altering the sequences to match the target gene. Furthermore multiple trap-RNA systems can applied to the same biological circuit without interfering. Implementing sRNA and the trap-RNA into biological constructs they can be introduced by constitutive promoters or inducible promoters.