Team:Austin UTexas/Project/Problem
Problem: Genetic Instability
Background
One of the major issue facing genetic engineering is the overall longevity of genetic devices once inserted into organisms. An organism can be modified, but that does not ensure that the modification will last. Subsequent generations of modified organisms often lose or “break” the genetic device through mutations. Mutations that cause the inactivation of a plasmid or an inserted device decrease the metabolic load of that organism and allow the mutant and its descendants to replicate and grow faster than the originally modified organism, allowing the “broken” mutant to overtake a population. Previous research has determined several factors that contribute to the breaking of genetic devices. A major source is the level of expression and overall metabolic cost of the genetic insert to the organism. Strongly expressed devices will break faster than lower levels of expression; furthermore, a genetic device that leads to a more complex and resource costly protein is more prone to breakage. Another major factor that contributes to generational stability is sequence repeats and homology in the sequence of the genetic device. If a particular sequence contains many short sequence repeats or even large, similar regions, then that sequence risks instability in later generations.
The stability of the sequence is the focus of our research over the course of the summer. We wish to identify sequences that contribute to the relative instability of genetic devices so they can be used to predict device longevity, as well as be taken into account when creating and modifying such devices. In the spring of 2015, E. coli was transformed using various fluorescent genes and monitored for breakage, with varying results depending on the plasmid used. Three plasmids were selected from the spring experiment to be used. All three plasmids used the pSB1C3 backbone and the vector BioBrick BBa_K608006, composed of a medium promoter (J23110) and medium ribosome binding site (B0032). Each plasmid then differed by the fluorescent protein used: Yellow fluorescent protein (BBa_K592101), Super-folder Yellow fluorescent protein (BBa_K864100), and Engineered Yellow fluorescence protein (BBa_E0030). The YFP plasmid was to shown, during the spring, was shown to accumulate various insertions and deletions in the YFP gene that would lead to its breakage. The Super-folder YFP plasmid was broken by a large insertion after the promoter sequence that led the breakdown of expression. Finally, the engineered-YFP gene, which was codon optimized from the original YFP sequence, did not accumulate mutations or break over the course of ten days.
Over the summer, these three plasmids were used to transform four strains of bacteria (Top-10, MDS-42, BL-21 (DE3), BW-25113). Growing these transformed strains in culture and monitoring their fluorescence and stability will hopefully elucidate more regarding patterns in the sequences that contribute to the instability of genetic devices. Understanding this could lead to more stable devices and thus could increase the longevity of genetically modified organisms.