Difference between revisions of "Part:BBa K3081042"
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<partinfo>BBa_K3081042 short</partinfo>
 
<partinfo>BBa_K3081042 short</partinfo>
  
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This composite part is the principal design of the inducible CRISPR-based DNA replication interference system, with the 20 bp sgRNA targeting to the initiation site on p15A origin. In this part, we add a degradation signal peptide "ssrA" to the dCas9 to alleviate its effect.  
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This composite part uses a CRISPR-based DNA replication interference system for the copy number control of the p15A plasmid. The dCas9 is expressed in an inducible manner with a ssrA degradation tag fused to its C-terminal to minimize the basal expression. The sgRNA has a 20-bp complementary sequence with the template strand of replication activator (RNA II) in p15A origin. However, it shows no effect for some unknown reasons.
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<center>
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https://2019.igem.org/wiki/images/c/ca/T--Peking--p15A_mechanism.png
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</center>
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<center>
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<b>Design of the p15A plasmid copy number control system</b>
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</center>
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<center>
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https://2019.igem.org/wiki/images/f/fa/T--Peking--p15A_result.png
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</center>
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<center>
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<b>The effect of 4 target sites on p15A origin</b>
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</center>
  
  

Revision as of 14:05, 21 October 2019

CRISPR-based replication interference system for p15A plasmid copy number control, RNA II site

This composite part uses a CRISPR-based DNA replication interference system for the copy number control of the p15A plasmid. The dCas9 is expressed in an inducible manner with a ssrA degradation tag fused to its C-terminal to minimize the basal expression. The sgRNA has a 20-bp complementary sequence with the template strand of replication activator (RNA II) in p15A origin. However, it shows no effect for some unknown reasons.

T--Peking--p15A_mechanism.png

Design of the p15A plasmid copy number control system

T--Peking--p15A_result.png

The effect of 4 target sites on p15A origin


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 1205
    Illegal NheI site found at 2321
    Illegal NheI site found at 5495
    Illegal NheI site found at 5518
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1144
    Illegal BamHI site found at 4600
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 979
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 961