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Team:Imperial College London/Software
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<p><i>Figure 1: </i>Arabidopsis<i> plant grown in soil during our <a href="https://2011.igem.org/Team:Imperial_College_London/Project_Auxin_Testing"><b>soil erosion experiment</b></a>. (Picture by Imperial College iGEM team 2011.)</i></p> | <p><i>Figure 1: </i>Arabidopsis<i> plant grown in soil during our <a href="https://2011.igem.org/Team:Imperial_College_London/Project_Auxin_Testing"><b>soil erosion experiment</b></a>. (Picture by Imperial College iGEM team 2011.)</i></p> | ||
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<h2>Future Work:</h2> | <h2>Future Work:</h2> | ||
Revision as of 02:36, 22 September 2011
Software
Motivation:
We wanted the flexibility to express the genes responsible for auxin production in both B.subtilis and E.coli. To achieve this, we decided to joint codon optimise the IaaM and IaaH coding sequences. Unfortunately, we could not find any software for this task and so wrote our own.
Theory:
The genetic code is redundant which means that multiple codons can encode the same amino acid. Synonymous codons are circumstantially decoded by the cellular machinery at different speeds. This phenomenon means that it is possible to increase protein yields by optimising codon usage. It is tempting to think that one could codon optimise a sequence by selectively using an organism’s preferred codons. This is commonly referred to as the "one amino acid-one codon" method. Unfortunately it does not work. Recent optimisation studies have highlighted the importance of maintaining a diverse codon population in a given coding sequence. This said, the inclusion of ‘rare codons’ has also been shown to dramatically reduce protein expression E.coli.
Solution:
In our approach to codon optimisation, we attempted to maintain codon diversity while simultaneously limiting rare codon inclusion. This was achieved by randomly selecting codons weighted by codon usage bias and then pruning the sequence of rare codons. The codon bias table used for this process was generated by combining those of E.coli and B.subtilis. Rare codon pruning was achieved by re-sampling synonymous codons to maintain sequence diversity. The script used for codon optimisation was written in R and can be downloaded below.
In-silico Testing:
To test our codon optimisation software, we ran the protein Dendra2 (BBa_K515007) through our software. The resultant DNA sequences were then fed into Genscript’s Codon Adaptation Index (CAI) analyser. This online tool measures the suitability of a sequence for expression in E.coli. Genscript’s own codon optimisation claims to be able to generate sequences with a CAI > 0.8. We were able to match this.
[[File:https://2011.igem.org/File:ICL_2011_CodonOptimisation.png]]
Figure 1: Arabidopsis plant grown in soil during our soil erosion experiment. (Picture by Imperial College iGEM team 2011.)
Future Work:
Recent work has suggested that rather than using codon frequency tables, it is better to use codons that are read by a subset of tRNAs that the most frequently charged during amino acid starvation. http://www.plosone.org/article/info:doi/10.1371/journal.pone.0007002 Once enough data is available for both E.coli and B.subtilis this data could be incorporated into the program.
http://www.microbialcellfactories.com/content/10/1/15/abstract
