IDEA!
Place sgRNAs under control of different light sensors. One light one sgRNA.
Our system operates like this:
1. light sensors regulates sgRNAs;
2. then sgRNAs regulate their corresponding genes, which is the final targets in the pathway to be optimized.
Therefore, we are able to:
In the past, researchers seldom accomplishes the regulation of genomic genes since it is so difficult to change endogenous promoters to be regulated by outer signals.
- Simultaneously controlling several genes.
Each gene is regulated by a different light, respectively.
- Offer a easy-to-use platform.
Users of our Metabolic Gear Box can optimize their own desired pathway after making some minor changes to a vector of sgRNAs.
Testing CRISPRi
To test CRISPRi, we have constructed a constitutive dCas9 on pRSFDuet, a constitutive sgRNA targeting mRFP (gR4mRFP) on pCDFDuet and a constitutive mRFP on pETDuet.
Then we set up a strictly controlled experiment as follows:
- Case: constitutive dCas9 on pRSFDuet + a constitutive gR4mRFP on pCDFDuet + constitutive mRFP on pETDuet
- Controll: constitutive dCas9 on pRSFDuet + an empty pCDFDuet + constitutive mRFP on pETDuet
As expected, mRFP repressed by CRISPRi (dCas9 and gR4mRFP) is not as red as the control.
Testing the Interface of CRISPRi and Light Sensors
To assure that CRISPRi can be successfully combined with Light Sensors. We constructed sgRNAs targeting mRFP that are regulated by red, green and blue light sensors, respectively.
Gathering Quantitative Data -- sgRNA targeting luciferase
In order to know whether our system provides a wide enough range of continuous adjustment, we constructed sgRNAs targeting luciferase (gR4luciferase) gene. And again, these gR4luciferase are under controll of red, green and blue light, respectively.
Designing a sgRNA targeting luciferase
Since we do not know the sequence of a working sgRNA that targets luciferase, so we designed two gR4mRFP ourselves according to those design criteria: one is closer to the start codon, whereas the other is relatively further.
However it is necessary for us to test these sgRNA. So we again inserted these two sgRNAs into a constitutive operon. After conducting a luciferase reporter assay with a Beyotime kit, it comes out that the repression effect of these two sgRNAs are 80% and 60%, respectively
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