Difference between revisions of "Part:BBa K1062001"
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__NOTOC__
 
__NOTOC__
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<partinfo>BBa_K1062000 short</partinfo>
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<partinfo>BBa_K1062001 short</partinfo>
  
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This part is a guide RNA (gRNA) that targets GFP, when bound to Cas9. It also contains a cleavage site recognized by the Csy4 enzyme which allows it to be cleaved from neighboring DNA/RNA.  
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This part is a guide RNA (gRNA) that targets the GFP gene, when bound to Cas9. It also contains a cleavage site recognized by the Csy4 enzyme which allows it to be cleaved from neighboring DNA/RNA.  
 
   
 
   
  
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K1062001 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K1062001 SequenceAndFeatures</partinfo>
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==='''Usage and Biology'''===
 
==='''Usage and Biology'''===
 
In both of our projects, we used gRNAs and dCas9 as:  
 
In both of our projects, we used gRNAs and dCas9 as:  
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1) To specifically target and repress the "virulence gene" (we used flourescent proteins as a proof of concept) in our conjugation project
 
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2) Improve past circuits with better decision making by using dCas9 instead of traditional repressors.
 
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However, the gRNA for GFP is not used in the conjugation project since the green fluorescent protein is to represent the donor strain of the project.
 
  
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[[File:Synthetic Circuit.jpg]]
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1) To specifically target and repress the "virulence gene" (we used flourescent proteins as a proof of concept) in our conjugation project. However, the gRNA for GFP is not used in the conjugation project since the green fluorescent protein was used to represent our donor strain of the project.
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 +
2) Improve past circuits with better decision making by using dCas9 instead of traditional repressors.
  
 
=='''Conjugation Project'''==
 
=='''Conjugation Project'''==
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'''The GFP gRNA was not used in the Conjugation Project'''
  
 
=='''Synthetic Circuit'''==
 
=='''Synthetic Circuit'''==
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[[File:Synthetic Circuit.jpg]]
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In the Synthetic Circuit, the target is the GFP gene that would be located in the '''Low Concentration Pathway'''. The purpose of the gRNA is to prevent any possibility of the GFP gene expressing, due to a possible leaky promoter, when the '''High Concentration Pathway''' is being induced.
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  
 
===Functional Parameters===
 
===Functional Parameters===
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<partinfo>BBa_K1062000 parameters</partinfo>
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<partinfo>BBa_K1062001 parameters</partinfo>
 
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Latest revision as of 09:08, 24 September 2013

Guide RNA (gRNA) target for GFP

This part is a guide RNA (gRNA) that targets the GFP gene, when bound to Cas9. It also contains a cleavage site recognized by the Csy4 enzyme which allows it to be cleaved from neighboring DNA/RNA.


Sequence and Features


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]


Usage and Biology

In both of our projects, we used gRNAs and dCas9 as:

1) To specifically target and repress the "virulence gene" (we used flourescent proteins as a proof of concept) in our conjugation project. However, the gRNA for GFP is not used in the conjugation project since the green fluorescent protein was used to represent our donor strain of the project.

2) Improve past circuits with better decision making by using dCas9 instead of traditional repressors.

Conjugation Project

The GFP gRNA was not used in the Conjugation Project

Synthetic Circuit

Synthetic Circuit.jpg

In the Synthetic Circuit, the target is the GFP gene that would be located in the Low Concentration Pathway. The purpose of the gRNA is to prevent any possibility of the GFP gene expressing, due to a possible leaky promoter, when the High Concentration Pathway is being induced.