Team:TUDelft/Temperature overview

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===Bacterial Thermometer===
===Bacterial Thermometer===
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====ROSE====
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''R''epressor ''O''f heat-''S''hock gene ''E''xpression (ROSE) is the (conserved) mRNA sequence found in front of some prokaryotic heat-shock proteins.[http://www.nature.com/emboj/journal/v25/n11/pdf/7601128a.pdf] Turning this into a biobrick should allow induction of translation by heating to 42 °C.
''R''epressor ''O''f heat-''S''hock gene ''E''xpression (ROSE) is the (conserved) mRNA sequence found in front of some prokaryotic heat-shock proteins.[http://www.nature.com/emboj/journal/v25/n11/pdf/7601128a.pdf] Turning this into a biobrick should allow induction of translation by heating to 42 °C.
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Revision as of 15:58, 25 August 2008

Contents

Bacterial Thermometer

We want to create an RNA-based system that is able to have differential gene expression when temperature changes take place (kind of similar to the Berkeley iGEM 2006 - riboregulator lock/key part [http://parts.mit.edu/wiki/index.php/Berkeley2006-RiboregulatorsMain]).

There are several systems suggested in literature that are based on RNA secondary structure. The idea in general is that if the temperature drops below a certain temperature, the RNA will form stable base-pairs on the Shine-Dalgarno sequence, disabling the ribosome to bind. The base-pairing of the RNA will impair the ability of the cell to express the protein encoded behind it. In this way gene expression can be regulated on the RNA level by temperature. The different ways that are described in literature are:

Virulence derived expression

Various pathogenic microorganisms express virulence proteins only inside a host. It has been shown in the 90's this is induced by the increased temperature having effect on translation but not on transcription [http://jb.asm.org/cgi/reprint/175/24/7901]. Examples of microorganisms using this temperature induced virulence are Salmonella [http://www3.interscience.wiley.com/cgi-bin/fulltext/118542064/PDFSTART], Yersinia pestis or Listeria monocytogenes. Of course we won't work with these virulent genes, only with the regulating mRNA sequences in front of them or their TF. An induction temperature of 37 °C seems logical.

(Designed)G-Quadruplex structures

As described by Wieland et al. [http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRP-4P8YWVM-7-8&_cdi=6240&_user=499885&_orig=search&_coverDate=07%2F30%2F2007&_sk=999859992&view=c&wchp=dGLbVzz-zSkzS&md5=97741390ae4ff0d9a8c4d5f41beb0f1d&ie=/sdarticle.pdf] it is possible to design sequences that form tertiary structures occluding the RBS. A temperature range of 30 - 35 °C has been achieved.

ROSE

Repressor Of heat-Shock gene Expression (ROSE) is the (conserved) mRNA sequence found in front of some prokaryotic heat-shock proteins.[http://www.nature.com/emboj/journal/v25/n11/pdf/7601128a.pdf] Turning this into a biobrick should allow induction of translation by heating to 42 °C.