Codon Optimization: Engineering a More Useful Gene at the Codon Level

Project Summary

Codons are groups of three nucleotides that specify a single amino acid, which is then added to a growing polypeptide chain during translation. Even though each codon spefifies only one amino acid, some amino acids are coded by multiple codons. It has been demonstrated that the genome of E.coli shows statistical preference for some of these degenerate codons over others, and it is hypothesized that these codons translate more efficiently than non preferred degenerate codons. We constructed synthetic reporter genes entirely from codons hypothesized to be fast or slow,and characterized them in E.coli, demonstrating that...

Why is this important?

Numerous bioproducts are important in our lives. Examples include medicines, fuels, and industrial chemicals. All of these are derived from biological sources, and the ability to engineer their production is vital to a wide variety of industries. Codon optimization is an important area of research because it has the potential to give engineers an additional point of control over protein synthesis, and proteins(a broad class of macromolecules that includes enzymes)are vital components of countless bioproducts.

Our codon optimization research is important for the additional reason that it will help future researchers to develop more comprehensive models of translation. A better understanding of translation is an example of a foundational advance in biology that will lead to faster, more efficient research in many areas of biology. If, for example, our research shows clearly that certain degenerate codons are preferred because they can be translated more efficiently this will allow scientists to search for a mechanism that predicts these effects, and will invite engineers to redesign genes to be translated more efficiently.

Background

Codon optimization refers to the idea that the individual codons of a gene in a specific organism can be changed in order to alter the behavior of that organism. This relies on an understanding of the central dogma of biology, which states that any organism produces proteins by first transcribing genetic material in the form of DNA to RNA, which is then “read” by ribosomes which produce proteins based on the sequence of amino acids in that RNA. The reading of the RNA is done three nucleotides at a time, and these three letter series of nucleotides are called codons. Codons specify to the ribosome which amino acid to add to a growing amino acid chain.

There are 4 nucleotides, thus 43, or 64 codons are possible. Since there are only 20 amino acids, there is redundancy in the codons, that is, some amino acids are specified by multiple codons. There is no ambiguity, however, meaning that each codon specifies only one amino acid. Codons that code for the same amino acid are called degenerate codons, and even though these degenerate codons code for the same amino acid, they do not necessarily lead to the same expression levels of that amino acid.

Our Objectives

1) Find Criteria for Optimizing Genes in E. coli

Previous researchers have determined through a statistical analysis of the entire genome that some degenerate codons occur more often in protein coding sequences and some are more infrequent. These are referred to as common and rare codons. The importance of this is that protein expression in cells is limited either by either translation initiation rate (TIR) or translation elongation rate, and it is theorized that commonly occurring codons will have faster elongation rates than degenerate rare codons. Translation initiation rate can be artificially controlled by varying the strength of the ribosome binding site (RBS), which consists of the genetic sequence that precedes the protein coding sequences (CDS) of a gene. This is accomplished through the use of the RBS calculator, and in previous research was used to steadily increase the RBS strength of a gene, GFP mut3b, the expression of which was then characterized. Unexpectedly, expression level of proteins plateaued even as the RBS strength (and thus TIR) was increased. By using the RBS Calculator to increase the translation initiation rate, we can detect when the plateau occurs, which is called the "maximum translation rate capacity." Since this plateau occurs independently of TIR, it is theorized that it is due solely to translation elongation becoming a rate limiting step

In another recent project, all the genes (coding DNA sequences) of E. coli are divided into five groups based on the naturally occurring TIR, from lowest to highest. Then, the codon usage profile of each group of genes is statistically analyzed to determine whether a codon is slow or fast. A fast codon is defined as one with high correlation between TIR and its frequency. Otherwise, it is a slow codon. It is hypothesized that the groups of CDS with high TIR will hold more “fast” codons, which will lead to higher translation elongation rate and thus higher protein expression, whereas the slow regions will hold more “slow” codons leading to lower expression.

2) Apply These Criteria to a Reporter Gene (GFP)

3) Introduce the Synthetic Genes Optimized Using Our Criteria into E. coli

4) Characterize the GFPs by Measuring Fluorescence of the Cells

5) Compare Protein Expression Levels from the Various Genes

Design Methods

The figure below shows the vector pFTV that was altered using inverse PCR.

Inverse PCR

Caption

Bold heading: