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Composite
Const gR4m

Part:BBa_K1026002

Designed by: Hongyi WU   Group: iGEM13_SJTU-BioX-Shanghai   (2013-09-16)
Revision as of 18:02, 27 September 2013 by Xuanguangzhulin (Talk | contribs)

Constitutively Expressed gRNA targeting mRFP

This Constitutively Expressed gRNA targeting mRFP is a no-BioBrick-scars assembly of the constitutive promoter BBa_J23100, DNA sequence of a gRNA that targets mRFP reporter and a reliable terminator BBa_B0015.


This gRNA sequence comes from the following literature: QI, LEI S., LARSON, MATTHEW H., GILBERT, LUKE A., DOUDNA, JENNIFER A., WEISSMAN, JONATHAN S., ARKIN, ADAM P. & LIM, WENDELL A. 2013. Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression. Cell, 152, 1173-1183.


In CRISPRi system, when dCas9 and gRNA bind together, they will bind to the specific DNA that has the complementary sequence of gRNA. We test this system using mRFP as a reporter gene.


There are two experimenting groups: e.coli in control group only expresses dCas9 and mRFP, and in case group it expresses dCas9, sgRNA and mRFP. And the result is shown as follows:


图片1.jpg


In case group, dCas9 did not affect the expression of mRFP; in control group, there is a significant knock down effect of mRFP.


All of these results are in consistent with our expectation.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


[edit]
Categories
//function/crispr
Parameters
None