Composite

Part:BBa_K3017065:Design

Designed by: Luk Hau Ching   Group: iGEM19_Hong_Kong_HKUST   (2019-10-17)


Construct for testing CRISPRi sgRNA suppression on fluorescence protein production


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 3147
    Illegal PstI site found at 4569
    Illegal PstI site found at 4773
    Illegal PstI site found at 4803
    Illegal PstI site found at 6015
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 2131
    Illegal NheI site found at 2303
    Illegal NheI site found at 2326
    Illegal PstI site found at 3147
    Illegal PstI site found at 4569
    Illegal PstI site found at 4773
    Illegal PstI site found at 4803
    Illegal PstI site found at 6015
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2608
    Illegal BamHI site found at 2070
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 3147
    Illegal PstI site found at 4569
    Illegal PstI site found at 4773
    Illegal PstI site found at 4803
    Illegal PstI site found at 6015
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 3147
    Illegal PstI site found at 4569
    Illegal PstI site found at 4773
    Illegal PstI site found at 4803
    Illegal PstI site found at 6015
    Illegal NgoMIV site found at 3435
    Illegal NgoMIV site found at 4539
    Illegal NgoMIV site found at 4612
    Illegal NgoMIV site found at 5097
    Illegal NgoMIV site found at 6006
    Illegal AgeI site found at 1905
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 705
    Illegal SapI site found at 1887


Design Notes

Source

dCas9 gene comes from Streptococcus pyogenes

References

Y. J. Lee, A. Hoynes-Oconnor, M. C. Leong, and T. S. Moon, “Programmable control of bacterial gene expression with the combined CRISPR and antisense RNA system,” Nucleic Acids Research, vol. 44, no. 5, pp. 2462–2473, Feb. 2016.

C. Anders, O. Niewoehner, A. Duerst, and M. Jinek, “Structural basis of PAM-dependent target DNA recognition by the Cas9 endonuclease,” Nature, vol. 513, no. 7519, pp. 569–573, 2014.

S. H. Sternberg, S. Redding, M. Jinek, E. C. Greene, and J. A. Doudna, “DNA Interrogation by the CRISPR RNA-Guided Endonuclease Cas9,” Biophysical Journal, vol. 106, no. 2, 2014.

T. Karvelis, G. Gasiunas, A. Miksys, R. Barrangou, P. Horvath, and V. Siksnys, “crRNA and tracrRNA guide Cas9-mediated DNA interference inStreptococcus thermophilus,” RNA Biology, vol. 10, no. 5, pp. 841–851, 2013.

T. Møller, T. Franch, P. Højrup, D. R. Keene, H. P. Bächinger, R. G. Brennan, and P. Valentin-Hansen, “Hfq,” Molecular Cell, vol. 9, no. 1, pp. 23–30, 2002.

G. M. Cech, A. Szalewska-Pałasz, K. Kubiak, A. Malabirade, W. Grange, V. Arluison, and G. Węgrzyn, “The Escherichia Coli Hfq Protein: An Unattended DNA-Transactions Regulator,” Frontiers in Molecular Biosciences, vol. 3, 2016.