Difference between revisions of "Part:BBa K5047028"

 
 
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<partinfo>BBa_K5047028 short</partinfo>
 
<partinfo>BBa_K5047028 short</partinfo>
  
This DNA sequence encodes a short hairpin RNA shRNA designed to target a specific region within the chitin synthase gene of the Asian hornet Vespa velutina. The target region is located on an exon common to all isoforms of the chitin synthase gene GeneID 124951980 Genbank XM_047501172.1 within the genomic coordinates NC_062188.1 19915311-19930067 iVesVel2.1 genome GCF_912470025.1. The specific target sequence spans from positions 19920482 to 19920507.  
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This DNA sequence encodes a short hairpin RNA shRNA designed to target a specific region within the chitin synthase gene of the Asian hornet Vespa velutina. The target region is located on an exon common to all isoforms of the chitin synthase gene GeneID 124951980 Genbank XM_047501172.1 within the genomic coordinates NC_062188.1 19915311-19930067 iVesVel2.1 genome GCF_912470025.1.  
  
This shRNA has been designed to keep GC content intermediate approx. 30 - 50% with 36% in this variant to avoid strong secondary structure. This sequence has off-targets in Vespa mandarinia and Vespa crabro with one mismatch INDEL and in Cerceris rybyensis and Anoplius nigerrimus with two mismatches in each.
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The specific target sequence spans from positions 19920482 to 19920507. This shRNA has been designed to keep GC content intermediate approx. 30 - 50% with 36% in this variant to avoid strong secondary structure. This sequence has off-targets in Vespa mandarinia and Vespa crabro with one mismatch INDEL and in Cerceris rybyensis and Anoplius nigerrimus with two mismatches in each.
  
This shRNA contains the optimized UGAUAUGUGCA loop Schopman Nick C T et al. Optimization of shRNA inhibitors by variation of the terminal loop sequence Antiviral research vol 86.2 2010 204-11 doi 101016jantiviral201002320.
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Upon testing in human embryonic kidney 293T cells using a luciferase assay, Schopman Nick C T et al. “Optimization of shRNA inhibitors by variation of the terminal loop sequence.” Antiviral Research vol. 86.2 (2010): 204-11. doi: 10.1016/j.antiviral.2010.02.320 reported that shRNAs based on the mir-17 and mir-25 loops exhibited the strongest target repression, approximately 10-fold stronger than the 9-nt loop.
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This shRNA contains the optimized UGAUAUGUGCA loop Schopman Nick C T et al. Optimization of shRNA inhibitors by variation of the terminal loop sequence Antiviral research vol 86.2 2010 204-11 doi: 10.1016/j.antiviral.2010.02.320.
 
Through secondary structure analysis performed by ViennaRNA the free energy of the thermodynamic ensemble is -42.40 kcalmol. The frequency of the minimum free energy structure in the ensemble is 51.90%. The ensemble diversity is 0.78.
 
Through secondary structure analysis performed by ViennaRNA the free energy of the thermodynamic ensemble is -42.40 kcalmol. The frequency of the minimum free energy structure in the ensemble is 51.90%. The ensemble diversity is 0.78.
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 18:15, 30 September 2024


DNA encodes a shRNA binds to chitin synthase gene of V. velutina.

This DNA sequence encodes a short hairpin RNA shRNA designed to target a specific region within the chitin synthase gene of the Asian hornet Vespa velutina. The target region is located on an exon common to all isoforms of the chitin synthase gene GeneID 124951980 Genbank XM_047501172.1 within the genomic coordinates NC_062188.1 19915311-19930067 iVesVel2.1 genome GCF_912470025.1.

The specific target sequence spans from positions 19920482 to 19920507. This shRNA has been designed to keep GC content intermediate approx. 30 - 50% with 36% in this variant to avoid strong secondary structure. This sequence has off-targets in Vespa mandarinia and Vespa crabro with one mismatch INDEL and in Cerceris rybyensis and Anoplius nigerrimus with two mismatches in each.

Upon testing in human embryonic kidney 293T cells using a luciferase assay, Schopman Nick C T et al. “Optimization of shRNA inhibitors by variation of the terminal loop sequence.” Antiviral Research vol. 86.2 (2010): 204-11. doi: 10.1016/j.antiviral.2010.02.320 reported that shRNAs based on the mir-17 and mir-25 loops exhibited the strongest target repression, approximately 10-fold stronger than the 9-nt loop.

This shRNA contains the optimized UGAUAUGUGCA loop Schopman Nick C T et al. Optimization of shRNA inhibitors by variation of the terminal loop sequence Antiviral research vol 86.2 2010 204-11 doi: 10.1016/j.antiviral.2010.02.320. Through secondary structure analysis performed by ViennaRNA the free energy of the thermodynamic ensemble is -42.40 kcalmol. The frequency of the minimum free energy structure in the ensemble is 51.90%. The ensemble diversity is 0.78.


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]