Team:MIT/Cas9-VP16

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Revision as of 02:48, 26 September 2013

iGEM 2012

Overview

  • Project Overview

miRNA Signal

  • Overview
  • siRNA Characterization
  • Exosome Isolation and Co-Culturing
  • Cell-Cell Co-Culturing

Protein Signals

  • Overview
  • GFP
  • rtTA3
  • Cre
  • L7Ae
  • Cas9-VP16

Novel DNA Sensor: Cas9 Split Venus Fusion

  • Overview
  • Leucine Zipper Fusion
  • DNA Sensing

Our BioBricks

  • Favorites
  • All BioBricks

Attributions

  • Attributions

Overview of Cas9

Cas9 is one of the proteins involved in the adaptive immune system (CRISPR system) of some bacteria and most archaea. In simple terms, the Cas9 functions by binding to a small hairpin RNA called a guide RNA. The Cas9-gRNA complex then scans the DNA for a sequence complementary to the 5' amino acids of the complexed guide RNA. Once a complementary region has been found, the Cas9 cuts the DNA at that location. The Cas9 we use has been mutated such that it still complexes with the guide RNA and targets the sequence complementary to the guide RNA, but the Cas9's nuclease activity has been eliminated. Once the Cas9 finds its target site, it simply stays put.

Cas9-VP16 Characterization

Here, we describe the creation and testing of a Cas9-VP16 fusion protein. Current transcriptional level activators/repressors function by binding DNA at certain conserved sequences and influencing the transcriptional abilities of some nearby promoter. The issue with these current activators/repressors is that each one binds one unique DNA sequence. The GAL protein binds UAS sites, TetR binds TetO sites, LacI binds LacO sites, and so on. By using Cas9 as the DNA binding portion of a trans-activator, we can eliminate the need for specific binding sites by taking advantage of Cas9's unique ability to target most any DNA sequence as determined by its complexed guide RNA. The technology could be used to either target and activate endogenous sequences by creating a guide RNA which targets a sequence upstream of the promoter in question, or one could create many different guide RNAs which target different inducible promoters and activate multiple genes with one single trans-activator. Our project looks into creating a Cas9-VP16 protein and testing its ability to activate a minimal CMV promoter by targeting the fusion to two upstream binding sites using a complementary guide RNA.

The Circuit



The U6_gRNA(Cr9) produces guide RNAs to target Cas9-VP16 to the Cr9 binding sites upstream of the minimal CMV promoter. When the Cas9-VP16 activator binds to the Cr9 sites, the minimal CMV promoter can be activated and eYFP is produced. TagBFP functions as our transfection marker.

The Data


The experimental procedure involved cotransfecting the genetic circuit shown above while varying the amount of transfected guide RNA (and using a dummy construct to keep a constant transfected DNA amount) to determine when we achieve optimal activation. The circuit was transfected into 200,000 HEK293 cells using Invitrogen Lipofectamine 2000 transfection reagent. The following set of data was gathered 72 hours post transfection via flow cytometry. The data is presented as median fluorescence values for subpopulations of cells grouped by intensity of transfection marker (normalizing fluorescence via plasmid count).