Project Description

	Synthetic biologists seek to control the behaviors, specifically those behaviors 
dictated by gene expression. To do this, they look to cells to provide a blueprint for their 
designs. However, scientists like Timothy Lu have noticed a distinct dichotomy in the field 
of synthetic biology surrounding cellular blue prints,

	“Living cells implement ... both analogue- and digital-like processing ... In contrast
to natural biological systems, synthetic biological systems have largely focused on either digital
or analogue computation separately.”

	Currently in the field, most methods of gene regulation are either digital (transcriptional
activators, repressors, and inducible circuits) or they are analog (oscillatory circuits). This 
summer our team desires to develop a synthetic promoter toolkit that can generate both digital and 
analog genetic expression.

	To do this, we have developed three main aims for our work this summer. The first aim is to 
develop a digital toolkit that is tunable, modular, and orthogonal. Tunable refers to a system with 
consistent replicable levels of gene expression similar across several activating complexes. Modular 
refers to a tolerance to several genes of interest and genetic architectures. Orthogonality refers a 
system that will not activate endogenous genes as well as produce cross talk over several activating 
complexes. The second aim is to develop the analog component of the toolkit by developing a grade
genetic expression. By this, we are referring to a system that can produce low, medium, and high levels 
of gene expression with the same level of accuracy as the digital component of the toolkit. Finally, our 
system must be able to function in the complex cellular environment of human cells to prepare it for 
ultimate use in therapies.

	To perform these task, we discussed the various methods by with gene expression can be 
modulated in cells. These techniques include Zinc Finger, TALEN, and CRISPR/dCas9. The decision was 
reached that CRISPR/dCas9 would be the tool of choice for our toolkit due to both its ease to engineer 
as well as its legacy in the foundational research category of iGEM (see Freiburg 2013).

	As a foundational advancement focused group, applications for our project are years off, however 
there are several speculative areas of interest. In many cases production of proteins harmful to host cells, 
like antibiotics, are difficult to do in large quantities due to the risk of death to host cells. By 
introducing a scalable response, scientists can increase efficiency without killing the host cell by properly 
finding the point at which the cells metabolism can no longer contend with the stress. In regards to 
therapeutics, this system could either allow doctors to properly dose a patient with gene expression in a 
similar way to how traditional pharmaceuticals functions. In addition, if this system was integrated with 
genetic logic circuits, the level of gene expression during a therapy could be theoretically modulated after
implantation to once again better address the needs of a patient.

Welcome to iGEM 2016!

Your team has been approved and you are ready to start the iGEM season!

Wiki template information

We have created these wiki template pages to help you get started and to help you think about how your team will be evaluated. You can find a list of all the pages tied to awards here at the Pages for awards link. You must edit these pages to be evaluated for medals and awards, but ultimately the design, layout, style and all other elements of your team wiki is up to you!