Difference between revisions of "Part:BBa K5047026"
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<partinfo>BBa_K5047026 short</partinfo> | <partinfo>BBa_K5047026 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 | + | 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 | + | The specific target sequence spans from positions 19925852 to 19925877. This shRNA has been designed to keep GC content intermediate approx. 30 - 50% with 44% in this variant to avoid strong secondary structure. This sequence has off-targets in Vespa mandarinia Dolichoris vasculosae and Gananspis Brasilliensis with one mismatch in each and in Vespa crabro with one INDEL. |
+ | 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 CCUCUCAACACUGG 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 -50.91 kcalmol. The frequency of the minimum free energy structure in the ensemble is 51.19%. The ensemble diversity is 0.77. | Through secondary structure analysis performed by ViennaRNA the free energy of the thermodynamic ensemble is -50.91 kcalmol. The frequency of the minimum free energy structure in the ensemble is 51.19%. The ensemble diversity is 0.77. | ||
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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 18:12, 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 19925852 to 19925877. This shRNA has been designed to keep GC content intermediate approx. 30 - 50% with 44% in this variant to avoid strong secondary structure. This sequence has off-targets in Vespa mandarinia Dolichoris vasculosae and Gananspis Brasilliensis with one mismatch in each and in Vespa crabro with one INDEL.
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 CCUCUCAACACUGG 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 -50.91 kcalmol. The frequency of the minimum free energy structure in the ensemble is 51.19%. The ensemble diversity is 0.77.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]