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The project aim to study how bacterial (e.coli) DNA organization can influence gene expression. In order to answer our question, the team decide to create a new tool based on CRISPR-Cas9 to bring together two distant DNA regions. This new tool is expected to assess the effect of DNA structure on gene expression. As a results, we have designed a linking tool and a visualization tool.

Here, we will expose you our experimental strategy, as well as, the biobricks we have designed to do so.

Linking tool construction

Visualization tool construction

Every system need an efficient control, as a result, a new part of the project has been setting up and the team has designed the visualization tool.

To build this new tool, two other ortholog nuclease function deficient Cas9s (dCas9s) : N.meningitidis and S.thermophilus, will be fused to fluorescent proteins.

We also decide to use dCas9 system for this tool in order to have detection of a accurate and unique sequence in the genome. It will be fulfilling with a new and unreleased in the iGEM competition tripartite slip-GFP. The tripartit split-GFP is composed of two twenty amino-acids long GFP tags (GFP10 and GFP11) and a third complementary subsection (GFP1-9). The tags will be fused to the two dCas9 previously quoted. A functional GFP will be achieved when the tools would be close enought to allow the three slip-GFP parts reunion and the fluorescence emission.

This fluorescence system avoids poor folding and/or self-assembly background fluorescence. With this system, only two sgRNAs associate with their dCas9s fused to their specific GFP tags will be necessary instead of nearly 30 with mundane GFP due to background fluorescence.

The team has designed three biobricks to achieve this part of the project.

• N.meningitidis fused to GFP-10 expressed by a constitutive promoter, a RBS and a double terminator
• S.thermophilus fused to GFP-11 expressed by a constitutive promoter, a RBS and a double terminator
• The third part of the GFP 1-9 expressed by a constitutive promoter, a RBS and a double terminator

Then, the team has considered to establish a composite biobrick composed of the three biobricks in the same pSB1C3 plasmid.

Characterization strategy

Tripartit Split-GFP and FRB/FKBP12 dimerization systems

Assessment of the minimal distance to have fluorescence

One of the goal of our project is to assess the system linking tool with the tri-partite GFP. To assess the effect of the linking tool, we have to know the minimal distance needed to such fluorescence emission. This question was also the core of our modeling part which answer the question “what is the optimal distance between the two dCas9 for fluorescence?”

This question is essential because the distance between the dCas9 may cause major problem. First, the steric hindrance and the dCas9 footprint may avoid the GFP assembling for target sequence too close. Second, the proteins size we have chosen avoid GFP assembling if there are too far away. As a result, fluorescence emission would be detect only if the proteins, as well as, the DNA regions are distant between a precise range of distance.

To assess experimentally such distant, the team has decided to designed different plasmids containing the visualization target sequences separate from each other with different distances. To do so, the team has designed specific primers to carry out RT-PCR and obtain from a plasmid in which the target sequences are distant with 1kB, different plasmids. The target sequence would be separate from :

• 1kB
• 500pB
• 150pB
• 75pB
• 50pB

Assessment of the DNA regions brought closer

Gene expression tests