Team:UNAM Genomics Mexico/Modeling/Cross Talk

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Revision as of 21:15, 26 September 2012


UNAM-Genomics_Mexico

=Cross Talk=

<img src="Unamgenomicsnanotubes.jpg" alt="some_text" height="200"/>

Nanotubes

<img src="Unamgenomicsnanotubes1.jpg" alt="some_text" height="200"/>

The logic

Random info




Due to the fact that our construction introduces exogenous transcription factors to the cell, we wanted to make sure that there would be no crosstalk, meaning that they wouldn’t recognize other promoters and create noise in the system. For this purpose, we downloaded weight matrixes for the sequences recognized by our transcription factors from PRODORIC database, and we downloaded the sequences for promoters (-200, +50 parting from the TSS) using retrieve sequence from RSA-tools. We chose Bacillus subtilis strain 168 because our strain is a derivative of this strain (I like the word strain…strain, strain, strain yay!). After that, we used quick matrix-scan in RSA-tools (Regulation Sequence Analysis-tools) to compare the sequences of the promoters to the weight matrixes to see if any of our transcription factors could bind in a troublesome place. We soon found out that this was not the case. Satisfied with our new-found self-confidence, we proceeded undauntedly to explore the more obscure parts of our project as our doubts wore away in the computational demonstration that they were, in fact, unworthy of being called truths. Here are the boring details of the deed: Details summary:

Tf

Sequence

Matches

AraC belonging to E. coli

Bacillus subtilis promoters

0

AraR belonging to B. subtilis

Pbad/Pxyl promoter

0

LasR belonging to P. aeruginosa

Bacillus subtilis promoters

0

XylR belonging to B. subtilits

Pbad promoter

0

XylR belonging to E. coli

Bacillus subtilis promoters

0