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Integrated siRNA design based on surveying of features associated with high RNAi effectiveness

BACKGROUND: Short interfering RNAs have allowed the development of clean and easily regulated methods for disruption of gene expression. However, while these methods continue to grow in popularity, designing effective siRNA experiments can be challenging. The various existing siRNA design guidelines...

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Autores principales: Gong, Wuming, Ren, Yongliang, Xu, Qiqi, Wang, Yejun, Lin, Dong, Zhou, Haiyan, Li, Tongbin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1698580/
https://www.ncbi.nlm.nih.gov/pubmed/17129386
http://dx.doi.org/10.1186/1471-2105-7-516
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author Gong, Wuming
Ren, Yongliang
Xu, Qiqi
Wang, Yejun
Lin, Dong
Zhou, Haiyan
Li, Tongbin
author_facet Gong, Wuming
Ren, Yongliang
Xu, Qiqi
Wang, Yejun
Lin, Dong
Zhou, Haiyan
Li, Tongbin
author_sort Gong, Wuming
collection PubMed
description BACKGROUND: Short interfering RNAs have allowed the development of clean and easily regulated methods for disruption of gene expression. However, while these methods continue to grow in popularity, designing effective siRNA experiments can be challenging. The various existing siRNA design guidelines suffer from two problems: they differ considerably from each other, and they produce high levels of false-positive predictions when tested on data of independent origins. RESULTS: Using a distinctly large set of siRNA efficacy data assembled from a vast diversity of origins (the siRecords data, containing records of 3,277 siRNA experiments targeting 1,518 genes, derived from 1,417 independent studies), we conducted extensive analyses of all known features that have been implicated in increasing RNAi effectiveness. A number of features having positive impacts on siRNA efficacy were identified. By performing quantitative analyses on cooperative effects among these features, then applying a disjunctive rule merging (DRM) algorithm, we developed a bundle of siRNA design rule sets with the false positive problem well curbed. A comparison with 15 online siRNA design tools indicated that some of the rule sets we developed surpassed all of these design tools commonly used in siRNA design practice in positive predictive values (PPVs). CONCLUSION: The availability of the large and diverse siRNA dataset from siRecords and the approach we describe in this report have allowed the development of highly effective and generally applicable siRNA design rule sets. Together with ever improving RNAi lab techniques, these design rule sets are expected to make siRNAs a more useful tool for molecular genetics, functional genomics, and drug discovery studies.
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spelling pubmed-16985802006-12-19 Integrated siRNA design based on surveying of features associated with high RNAi effectiveness Gong, Wuming Ren, Yongliang Xu, Qiqi Wang, Yejun Lin, Dong Zhou, Haiyan Li, Tongbin BMC Bioinformatics Research Article BACKGROUND: Short interfering RNAs have allowed the development of clean and easily regulated methods for disruption of gene expression. However, while these methods continue to grow in popularity, designing effective siRNA experiments can be challenging. The various existing siRNA design guidelines suffer from two problems: they differ considerably from each other, and they produce high levels of false-positive predictions when tested on data of independent origins. RESULTS: Using a distinctly large set of siRNA efficacy data assembled from a vast diversity of origins (the siRecords data, containing records of 3,277 siRNA experiments targeting 1,518 genes, derived from 1,417 independent studies), we conducted extensive analyses of all known features that have been implicated in increasing RNAi effectiveness. A number of features having positive impacts on siRNA efficacy were identified. By performing quantitative analyses on cooperative effects among these features, then applying a disjunctive rule merging (DRM) algorithm, we developed a bundle of siRNA design rule sets with the false positive problem well curbed. A comparison with 15 online siRNA design tools indicated that some of the rule sets we developed surpassed all of these design tools commonly used in siRNA design practice in positive predictive values (PPVs). CONCLUSION: The availability of the large and diverse siRNA dataset from siRecords and the approach we describe in this report have allowed the development of highly effective and generally applicable siRNA design rule sets. Together with ever improving RNAi lab techniques, these design rule sets are expected to make siRNAs a more useful tool for molecular genetics, functional genomics, and drug discovery studies. BioMed Central 2006-11-27 /pmc/articles/PMC1698580/ /pubmed/17129386 http://dx.doi.org/10.1186/1471-2105-7-516 Text en Copyright © 2006 Gong 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 Research Article
Gong, Wuming
Ren, Yongliang
Xu, Qiqi
Wang, Yejun
Lin, Dong
Zhou, Haiyan
Li, Tongbin
Integrated siRNA design based on surveying of features associated with high RNAi effectiveness
title Integrated siRNA design based on surveying of features associated with high RNAi effectiveness
title_full Integrated siRNA design based on surveying of features associated with high RNAi effectiveness
title_fullStr Integrated siRNA design based on surveying of features associated with high RNAi effectiveness
title_full_unstemmed Integrated siRNA design based on surveying of features associated with high RNAi effectiveness
title_short Integrated siRNA design based on surveying of features associated with high RNAi effectiveness
title_sort integrated sirna design based on surveying of features associated with high rnai effectiveness
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1698580/
https://www.ncbi.nlm.nih.gov/pubmed/17129386
http://dx.doi.org/10.1186/1471-2105-7-516
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