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siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse
RNA interference (RNAi) serves as a powerful and widely used gene silencing tool for basic biological research and is being developed as a therapeutic avenue to suppress disease-causing genes. However, the specificity and safety of RNAi strategies remains under scrutiny because small inhibitory RNAs...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592398/ https://www.ncbi.nlm.nih.gov/pubmed/22941647 http://dx.doi.org/10.1093/nar/gks797 |
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author | Boudreau, Ryan L. Spengler, Ryan M. Hylock, Ray H. Kusenda, Brandyn J. Davis, Heather A. Eichmann, David A. Davidson, Beverly L. |
author_facet | Boudreau, Ryan L. Spengler, Ryan M. Hylock, Ray H. Kusenda, Brandyn J. Davis, Heather A. Eichmann, David A. Davidson, Beverly L. |
author_sort | Boudreau, Ryan L. |
collection | PubMed |
description | RNA interference (RNAi) serves as a powerful and widely used gene silencing tool for basic biological research and is being developed as a therapeutic avenue to suppress disease-causing genes. However, the specificity and safety of RNAi strategies remains under scrutiny because small inhibitory RNAs (siRNAs) induce off-target silencing. Currently, the tools available for designing siRNAs are biased toward efficacy as opposed to specificity. Prior work from our laboratory and others’ supports the potential to design highly specific siRNAs by limiting the promiscuity of their seed sequences (positions 2–8 of the small RNA), the primary determinant of off-targeting. Here, a bioinformatic approach to predict off-targeting potentials was established using publically available siRNA data from more than 50 microarray experiments. With this, we developed a specificity-focused siRNA design algorithm and accompanying online tool which, upon validation, identifies candidate sequences with minimal off-targeting potentials and potent silencing capacities. This tool offers researchers unique functionality and output compared with currently available siRNA design programs. Furthermore, this approach can greatly improve genome-wide RNAi libraries and, most notably, provides the only broadly applicable means to limit off-targeting from RNAi expression vectors. |
format | Online Article Text |
id | pubmed-3592398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35923982013-03-08 siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse Boudreau, Ryan L. Spengler, Ryan M. Hylock, Ray H. Kusenda, Brandyn J. Davis, Heather A. Eichmann, David A. Davidson, Beverly L. Nucleic Acids Res Methods Online RNA interference (RNAi) serves as a powerful and widely used gene silencing tool for basic biological research and is being developed as a therapeutic avenue to suppress disease-causing genes. However, the specificity and safety of RNAi strategies remains under scrutiny because small inhibitory RNAs (siRNAs) induce off-target silencing. Currently, the tools available for designing siRNAs are biased toward efficacy as opposed to specificity. Prior work from our laboratory and others’ supports the potential to design highly specific siRNAs by limiting the promiscuity of their seed sequences (positions 2–8 of the small RNA), the primary determinant of off-targeting. Here, a bioinformatic approach to predict off-targeting potentials was established using publically available siRNA data from more than 50 microarray experiments. With this, we developed a specificity-focused siRNA design algorithm and accompanying online tool which, upon validation, identifies candidate sequences with minimal off-targeting potentials and potent silencing capacities. This tool offers researchers unique functionality and output compared with currently available siRNA design programs. Furthermore, this approach can greatly improve genome-wide RNAi libraries and, most notably, provides the only broadly applicable means to limit off-targeting from RNAi expression vectors. Oxford University Press 2013-01 2012-08-30 /pmc/articles/PMC3592398/ /pubmed/22941647 http://dx.doi.org/10.1093/nar/gks797 Text en Published by Oxford University Press 2012. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Boudreau, Ryan L. Spengler, Ryan M. Hylock, Ray H. Kusenda, Brandyn J. Davis, Heather A. Eichmann, David A. Davidson, Beverly L. siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse |
title | siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse |
title_full | siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse |
title_fullStr | siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse |
title_full_unstemmed | siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse |
title_short | siSPOTR: a tool for designing highly specific and potent siRNAs for human and mouse |
title_sort | sispotr: a tool for designing highly specific and potent sirnas for human and mouse |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592398/ https://www.ncbi.nlm.nih.gov/pubmed/22941647 http://dx.doi.org/10.1093/nar/gks797 |
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