sh-mir designer2013.igem.org › files › poster › amu-poznan.pdf · 2013-11-18 · 1.structure...

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Input: One strand or two strands in 5'-3' orientation of siRNA of known efficiency Concatenation of both given siRNA strands (or one given strand and one added) with flanking sequences and loop sequence of pri-miRNA (caps) taken from created pri-miRNA database. Analysis of sh-miRNA structure with mfold program. Comparison with structure of endogenous pri-miRNAs aggcaagaugcuggcauagcu ugcuaugccaacauauugccau CAUAACAACGAAGAGGGAUGGUAUUGCUCCUGUAACUCGGAACUGG AGAGGaggcaagaugcuggcauagcuGUUGAACUGGGAACCugcuaugccaacaua uugccauCUUUCCUGUCUGACAGCAGCUUGGCUACCUCCGUCCUGUUC CUCCUUGUCUU sh-miR Designer is a soware aimed for fast and efficient design of effecve RNA interference (RNAi) reagents - sh-miRs, also known as arficial miRNAs. sh-miRs are RNA parcles whose structure is based on miRNA precursor pri-miRNA, but sequence interacng with transcript is changed depending on research purpose. Maintenance of structure of pri-miRNA is very important to enable cellular processing (performed mainly by endonucleases Drosha and Dicer) and therefore ensure funconality of arficial parcles. sh- miRs delivered to cells on genec vectors - plasmids or viral vectors - enter natural RNAi pathway and silence target mRNA. They can be used in genec therapies and basic biomedical research. pri-miRNA database Scoring: 1.Structure 2.Same first nucleotides of siRNA and miRNA sequence 3.Endogenous pri-miRNA product homogeneity (isomirs) Output: 2-3 sh-miRs with best scoring results ordered from the best one pdf with 2D structure web link to miRbase site of pri-miRNA, which flanking sequences where used 'name': name, 'flanks3_s': flanks3_s, 'flanks3_a': flanks3_a, 'flanks5_s': flanks5_s, 'flanks5_a': flanks5_a, 'loop_s': loop_s, 'loop_a': loop_a, 'miRNA_s': miRNA_s, 'miRNA_a': miRNA_a, 'miRNA_length': miRNA_length, 'miRNA_min': miRNA_min, 'miRNA_max': miRNA_max, 'miRNA_end_5': miRNA_end_5, 'miRNA_end_3': miRNA_end_3, 'structure': structure, 'homogeneity': homogeneity, 'miRBase_link': miRBase_link 155 pri-miRNA A G G C U U G C U G U A G G C U G U A U G C U G U U U G U A U U C A G C C C A U A G C G C U U U U G C C U C C A A C U G G C G C U A U G G C G A A U A C A A A C A G U G U A U G A U G C C U G U U A C U A G C A U U C A C A U G G A A C A A A U U G C U G C C G U G G G A G G A U G A C A A A G A 5’ 3’ 20 40 60 80 100 120 140 A G G C U U G C U G U A G G C U G U A U G C U G U U A A U G C U A A U C G U G A U A G G G G U U U U G C C U C C A A C U G A C U C C U A C A U A U U A G C A U U A A C A G U G U A U G A U G C C U G U U A C U A G C A U U C A C A U G G A A C A A A U U G C U G C C G U G G G A G G A U G A C A A A G A 5’ 3’ 20 40 60 80 100 120 140 Drosha cut sh-miR designer Dicer cut tool for construction of RNA interference reagents: sh-miRs sh-miRNA with siRNA targeted on luciferase transcript in 155 pri-miRNA flansking sequence

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Page 1: sh-miR designer2013.igem.org › files › poster › AMU-Poznan.pdf · 2013-11-18 · 1.Structure 2.Same first nucleotides of siRNA and miRNA sequence 3.Endogenous pri-miRNA product

Input:One strand or two strands in 5'-3' orientation of siRNA of known efficiency

Concatenation of both given siRNA strands (or one given strand and one added) with flanking sequences and loop sequence of pri-miRNA (caps) taken from created pri-miRNA database.

Analysis of sh-miRNA structure with mfold program. Comparison with structure of endogenous pri-miRNAs

aggcaagaugcuggcauagcuugcuaugccaacauauugccau

CAUAACAACGAAGAGGGAUGGUAUUGCUCCUGUAACUCGGAACUGGAGAGGaggcaagaugcuggcauagcuGUUGAACUGGGAACCugcuaugccaacauauugccauCUUUCCUGUCUGACAGCAGCUUGGCUACCUCCGUCCUGUUCCUCCUUGUCUU

sh-miR Designer is a so�ware aimed for fast and efficient design of effec�ve RNA interference (RNAi) reagents - sh-miRs, also known as ar�ficial miRNAs. sh-miRs are RNA par�cles whose structure is based on miRNA precursor pri-miRNA, but sequence interac�ng with transcript is changed depending on research purpose. Maintenance of structure of pri-miRNA is very important to enable cellular processing (performed mainly by endonucleases Drosha and Dicer) and therefore ensure func�onality of ar�ficial par�cles. sh-miRs delivered to cells on gene�c vectors - plasmids or viral vectors - enter natural RNAi pathway and silence target mRNA. They can be used in gene�c therapies and basic biomedical research.

pri-miRNAdatabase

Scoring:1.Structure2.Same first nucleotides of siRNA and miRNA sequence3.Endogenous pri-miRNA product homogeneity (isomirs)

Output:2-3 sh-miRs with best scoring results ordered from the best onepdf with 2D structureweb link to miRbase site of pri-miRNA, which flanking sequences where used

'name': name, 'flanks3_s': flanks3_s, 'flanks3_a': flanks3_a, 'flanks5_s': flanks5_s, 'flanks5_a': flanks5_a, 'loop_s': loop_s, 'loop_a': loop_a, 'miRNA_s': miRNA_s, 'miRNA_a': miRNA_a, 'miRNA_length': miRNA_length, 'miRNA_min': miRNA_min, 'miRNA_max': miRNA_max, 'miRNA_end_5': miRNA_end_5, 'miRNA_end_3': miRNA_end_3, 'structure': structure, 'homogeneity': homogeneity, 'miRBase_link': miRBase_link

155 pri-miRNA

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Drosha cut

sh-miR designer

Dicer cut

tool for construction of RNA interference reagents: sh-miRs

sh-miRNA with siRNA targeted on luciferase transcriptin 155 pri-miRNA flansking sequence