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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...

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Autores principales: Boudreau, Ryan L., Spengler, Ryan M., Hylock, Ray H., Kusenda, Brandyn J., Davis, Heather A., Eichmann, David A., Davidson, Beverly L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
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.
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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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