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Off-target effects of siRNA specific for GFP

BACKGROUND: Gene knock down by RNAi is a highly effective approach to silence gene expression in experimental as well as therapeutic settings. However, this widely used methodology entails serious pitfalls, especially concerning specificity of the RNAi molecules. RESULTS: We tested the most widely u...

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Autores principales: Tschuch, Cordula, Schulz, Angela, Pscherer, Armin, Werft, Wiebke, Benner, Axel, Hotz-Wagenblatt, Agnes, Barrionuevo, Leticia Serra, Lichter, Peter, Mertens, Daniel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443166/
https://www.ncbi.nlm.nih.gov/pubmed/18577207
http://dx.doi.org/10.1186/1471-2199-9-60
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author Tschuch, Cordula
Schulz, Angela
Pscherer, Armin
Werft, Wiebke
Benner, Axel
Hotz-Wagenblatt, Agnes
Barrionuevo, Leticia Serra
Lichter, Peter
Mertens, Daniel
author_facet Tschuch, Cordula
Schulz, Angela
Pscherer, Armin
Werft, Wiebke
Benner, Axel
Hotz-Wagenblatt, Agnes
Barrionuevo, Leticia Serra
Lichter, Peter
Mertens, Daniel
author_sort Tschuch, Cordula
collection PubMed
description BACKGROUND: Gene knock down by RNAi is a highly effective approach to silence gene expression in experimental as well as therapeutic settings. However, this widely used methodology entails serious pitfalls, especially concerning specificity of the RNAi molecules. RESULTS: We tested the most widely used control siRNA directed against GFP for off-target effects and found that it deregulates in addition to GFP a set of endogenous target genes. The off-target effects were dependent on the amount of GFP siRNA transfected and were detected in a variety of cell lines. Since the respective siRNA molecule specific for GFP is widely used as negative control for RNAi experiments, we studied the complete set of off-target genes of this molecule by genome-wide expression profiling. The detected modulated mRNAs had target sequences homologous to the siRNA as small as 8 basepairs in size. However, we found no restriction of sequence homology to 3'UTR of target genes. CONCLUSION: We can show that even siRNAs without a physiological target have sequence-specific off-target effects in mammalian cells. Furthermore, our analysis defines the off-target genes affected by the siRNA that is commonly used as negative control and directed against GFP. Since off-target effects can hardly be avoided, the best strategy is to identify false positives and exclude them from the results. To this end, we provide the set of false positive genes deregulated by the commonly used GFP siRNA as a reference resource for future siRNA experiments.
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spelling pubmed-24431662008-07-04 Off-target effects of siRNA specific for GFP Tschuch, Cordula Schulz, Angela Pscherer, Armin Werft, Wiebke Benner, Axel Hotz-Wagenblatt, Agnes Barrionuevo, Leticia Serra Lichter, Peter Mertens, Daniel BMC Mol Biol Research Article BACKGROUND: Gene knock down by RNAi is a highly effective approach to silence gene expression in experimental as well as therapeutic settings. However, this widely used methodology entails serious pitfalls, especially concerning specificity of the RNAi molecules. RESULTS: We tested the most widely used control siRNA directed against GFP for off-target effects and found that it deregulates in addition to GFP a set of endogenous target genes. The off-target effects were dependent on the amount of GFP siRNA transfected and were detected in a variety of cell lines. Since the respective siRNA molecule specific for GFP is widely used as negative control for RNAi experiments, we studied the complete set of off-target genes of this molecule by genome-wide expression profiling. The detected modulated mRNAs had target sequences homologous to the siRNA as small as 8 basepairs in size. However, we found no restriction of sequence homology to 3'UTR of target genes. CONCLUSION: We can show that even siRNAs without a physiological target have sequence-specific off-target effects in mammalian cells. Furthermore, our analysis defines the off-target genes affected by the siRNA that is commonly used as negative control and directed against GFP. Since off-target effects can hardly be avoided, the best strategy is to identify false positives and exclude them from the results. To this end, we provide the set of false positive genes deregulated by the commonly used GFP siRNA as a reference resource for future siRNA experiments. BioMed Central 2008-06-24 /pmc/articles/PMC2443166/ /pubmed/18577207 http://dx.doi.org/10.1186/1471-2199-9-60 Text en Copyright © 2008 Tschuch 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
Tschuch, Cordula
Schulz, Angela
Pscherer, Armin
Werft, Wiebke
Benner, Axel
Hotz-Wagenblatt, Agnes
Barrionuevo, Leticia Serra
Lichter, Peter
Mertens, Daniel
Off-target effects of siRNA specific for GFP
title Off-target effects of siRNA specific for GFP
title_full Off-target effects of siRNA specific for GFP
title_fullStr Off-target effects of siRNA specific for GFP
title_full_unstemmed Off-target effects of siRNA specific for GFP
title_short Off-target effects of siRNA specific for GFP
title_sort off-target effects of sirna specific for gfp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443166/
https://www.ncbi.nlm.nih.gov/pubmed/18577207
http://dx.doi.org/10.1186/1471-2199-9-60
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