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Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules
OBJECTIVE: Here we report the improved results of a new siRNA design program and analysis tool called siRNA_profile that reveals an additional criterion for bioinformatic search of highly functional siRNA sequences. METHODS: We retrospectively analysed over 2400 siRNA sequences from 34 genes and wit...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2424050/ https://www.ncbi.nlm.nih.gov/pubmed/18495017 http://dx.doi.org/10.1186/1751-0473-3-8 |
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author | Muhonen, Pirkko Parthasarathy, Ranga N Janckila, Anthony J Büki, Kalman G Väänänen, H Kalervo |
author_facet | Muhonen, Pirkko Parthasarathy, Ranga N Janckila, Anthony J Büki, Kalman G Väänänen, H Kalervo |
author_sort | Muhonen, Pirkko |
collection | PubMed |
description | OBJECTIVE: Here we report the improved results of a new siRNA design program and analysis tool called siRNA_profile that reveals an additional criterion for bioinformatic search of highly functional siRNA sequences. METHODS: We retrospectively analysed over 2400 siRNA sequences from 34 genes and with known efficacies to categorize factors that differentiate highly, moderately and non-functional siRNA sequences in more detail. We tested the biological relevance of siRNA_profile in CHO cells stably expressing human TRACP. RESULTS: The highly functional siRNA molecules exhibited lower overall stabilities than non-functional siRNAs after taking into consideration all the nucleotides from 5'-terminus to the 3'-terminus along the siRNA molecule, in addition to the 5'-section of the antisense strand and the region between 9–14 nucleotides as previously has been acknowledged. Comparison of the siRNA_profile program to five other programs resulted in a wide range of selected siRNA sequences with diverse gene silencing capacities, even when the target was only 197 nucleotides long. Six siRNA design programs selected 24 different siRNA sequences, and only 6 of them were selected by two or more programs. The other 18 sequences were individually selected by these six programs. CONCLUSION: Low general stability of dsRNA plays a significant role in the RNAi pathway and is a recommended criterion to consider, in addition to 5'-instability, internal instability, nucleotide preferences and target mRNA position, when designing highly efficient siRNAs. |
format | Text |
id | pubmed-2424050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24240502008-06-11 Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules Muhonen, Pirkko Parthasarathy, Ranga N Janckila, Anthony J Büki, Kalman G Väänänen, H Kalervo Source Code Biol Med Brief Reports OBJECTIVE: Here we report the improved results of a new siRNA design program and analysis tool called siRNA_profile that reveals an additional criterion for bioinformatic search of highly functional siRNA sequences. METHODS: We retrospectively analysed over 2400 siRNA sequences from 34 genes and with known efficacies to categorize factors that differentiate highly, moderately and non-functional siRNA sequences in more detail. We tested the biological relevance of siRNA_profile in CHO cells stably expressing human TRACP. RESULTS: The highly functional siRNA molecules exhibited lower overall stabilities than non-functional siRNAs after taking into consideration all the nucleotides from 5'-terminus to the 3'-terminus along the siRNA molecule, in addition to the 5'-section of the antisense strand and the region between 9–14 nucleotides as previously has been acknowledged. Comparison of the siRNA_profile program to five other programs resulted in a wide range of selected siRNA sequences with diverse gene silencing capacities, even when the target was only 197 nucleotides long. Six siRNA design programs selected 24 different siRNA sequences, and only 6 of them were selected by two or more programs. The other 18 sequences were individually selected by these six programs. CONCLUSION: Low general stability of dsRNA plays a significant role in the RNAi pathway and is a recommended criterion to consider, in addition to 5'-instability, internal instability, nucleotide preferences and target mRNA position, when designing highly efficient siRNAs. BioMed Central 2008-05-21 /pmc/articles/PMC2424050/ /pubmed/18495017 http://dx.doi.org/10.1186/1751-0473-3-8 Text en Copyright © 2008 Muhonen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Reports Muhonen, Pirkko Parthasarathy, Ranga N Janckila, Anthony J Büki, Kalman G Väänänen, H Kalervo Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules |
title | Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules |
title_full | Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules |
title_fullStr | Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules |
title_full_unstemmed | Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules |
title_short | Analysis by siRNA_profile program displays novel thermodynamic characteristics of highly functional siRNA molecules |
title_sort | analysis by sirna_profile program displays novel thermodynamic characteristics of highly functional sirna molecules |
topic | Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2424050/ https://www.ncbi.nlm.nih.gov/pubmed/18495017 http://dx.doi.org/10.1186/1751-0473-3-8 |
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