CRISPR/Cas9 has been extensively studied for its applications in eukaryotic genome editing and gene expression control. Last year, the Waterloo iGEM team created an ODE model of dCas9 binding and control of gene expression. This year, however, the modelling team chose to investigate the effects of CRISPR/Cas9 on an genomic rather than molecular level. Specifically, we wanted to model the accumulation of mutations in a target genome and eventual deactivation of target genes after cutting by CRISPR/Cas9 and repair by Non-Homologous End Joining (NHEJ).

The Cas9 nuclease creates double-stranded breaks (DSBs) 3-4 bp upstream of the PAM site adjacent to its sgRNA . In the absence of a template, the DSBs will be repaired by Non-Homologous End Joining (NHEJ), which is an error-prone process that sometimes creates indels at the site of repair . This effect has recently been exploited to target double-stranded viruses such as HBV . Though there have been extensive effort to characterize the factors that contribute to effective targeting and deactivation by CRISPR/Cas9 and NHEJ, they have not, to the best of our knowledge, been incorporated into a single tool. This model aims to synthesize the characterixa

Model Formation

Probability of Double-Stranded Cuts made by CRISPR/Cas9

Taking into account target effects

Possible Outcomes After a Double-Stranded Break

Error-Prone Repair by NHEJ

Indel Probabilities

Large Deletions

Other Model Parameters

Talk about where all the probabilities come from

Results

Model Validation

Include notes on how the model matches reality/our expectations of reality in this section.

Simulate w/ targets that mismatch to different extents.

Effect of sgRNA Strength

Matt visualizations for different sgRNAs.

Graph of 3 different sgRNA designs of different strengths, show % functional

Importance of Large Deletions

Include notes on how the model matches reality/our expectations of reality in this section.

Effect of Cas9 Concentration

Include notes on how the model matches reality/our expectations of reality in this section.

Predicting CRISPR Plant Defense

This model was applied to the CRISPR Plant Defense aspect of our project, investigating whether the P6 protein of Cauliflower Mosaic Virus (CaMV) could be deactivated by frameshift mutations. The P6 protein was chosen as a focus of the investigation because it suppresses natural plant RNAi defenses and trans-activates translation of other CaMV proteins . Details on P6 and the CaMV genome can be found on CaMV Biology page.

The model was run with HOW MANY targets in the P6 gene of the simulated CaMV genome described above. We tracked the percent of simulated genomes with functional P6 across 1000 runs fo the model, giving a general prediction of how long it will take before the P6 of a particular CaMV genome is rendered non-functional by our Plant Defense system.

PLOT % functional for P6/time over many simulations.

Discussion

References