Difference between revisions of "Part:BBa K1062000:Design"

(→‎Design Notes)
(→‎Design Notes)
Line 15: Line 15:
 
An image show a general picture of a gRNA.
 
An image show a general picture of a gRNA.
  
−
The gRNA contains a CSY4 cut site that is essential to create the gRNA. Including in the part is a 20 nucleotide sequence that is targets specifically the RFP gene itself.
+
The CSY4 cut site is a sequence that is essential to the creation of the gRNA.
  
 
===Sources===
 
===Sources===

Revision as of 18:56, 10 September 2013


Guide RNA (gRNA) target for RFP


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Part:BBa_K1062000 is a gRNA containing a CSY4 cut site and specifically targets the RFP gene.

A gRNA is a 102 nt sequence in which contains: a 20 nt sequence which will contain the sequence of the intended target, a 42 nt Cas9-binding hairping, and a 40 nt transcription terminator.

GRNA-crop.png An image show a general picture of a gRNA.

The CSY4 cut site is a sequence that is essential to the creation of the gRNA.

Sources

The RFP gRNA was retrieved from Stanley Qi's Lab at UCSF.

References

Currently Stanley Qi's lab is doing research in which hopes to use the CRISPR system in new applications.

[http://www.ncbi.nlm.nih.gov/pubmed/23452860 Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression ]

In the paper in the link provided, Stanley had shown to control gene expression using the CRISPR system using GFP and RFP as proof of concept. The RFP gRNA being used in our project is the same gRNA Stanley used in this paper.