Off-target effects of siRNA specific for GFP

被引:69
作者
Tschuch, Cordula [1 ]
Schulz, Angela [1 ]
Pscherer, Armin [1 ]
Werft, Wiebke [2 ]
Benner, Axel [2 ]
Hotz-Wagenblatt, Agnes [3 ]
Barrionuevo, Leticia Serra [1 ]
Lichter, Peter [1 ]
Mertens, Daniel [1 ,4 ]
机构
[1] German Canc Res Ctr, Div Mol Genet, D-6900 Heidelberg, Germany
[2] German Canc Res Ctr, Div Biostat, D-6900 Heidelberg, Germany
[3] German Canc Res Ctr, Div Mol Biophys, D-6900 Heidelberg, Germany
[4] Univ Hosp, Dept Internal Med 3, Ulm, Germany
来源
BMC MOLECULAR BIOLOGY | 2008年 / 9卷
关键词
D O I
10.1186/1471-2199-9-60
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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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页数:14
相关论文
共 34 条
[1]   MicroRNAs silence gene expression by repressing protein expression and/or by promoting mRNA decay [J].
Behm-Ansmant, I. ;
Rehwinkel, J. ;
Izaurralde, E. .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2006, 71 :523-530
[2]   3′ UTR seed matches, but not overall identity, are associated with RNAi off-targets [J].
Birmingham, A ;
Anderson, EM ;
Reynolds, A ;
Ilsley-Tyree, D ;
Leake, D ;
Fedorov, Y ;
Baskerville, S ;
Maksimova, E ;
Robinson, K ;
Karpilow, J ;
Marshall, WS ;
Khvorova, A .
NATURE METHODS, 2006, 3 (03) :199-204
[3]   Improved silencing properties using small internally segmented interfering RNAs [J].
Bramsen, Jesper B. ;
Laursen, Maria B. ;
Damgaard, Christian K. ;
Lena, Suzy W. ;
Babu, B. Ravindra ;
Wengel, Jesper ;
Kjems, Jorgen .
NUCLEIC ACIDS RESEARCH, 2007, 35 (17) :5886-5897
[4]   Induction of an interferon response by RNAi vectors in mammalian cells [J].
Bridge, AJ ;
Pebernard, S ;
Ducraux, A ;
Nicoulaz, AL ;
Iggo, R .
NATURE GENETICS, 2003, 34 (03) :263-264
[5]   Enzymatically prepared RNAi libraries [J].
Buchholz, Frank ;
Kittler, Ralf ;
Slabicki, Mikolaj ;
Theis, Mirko .
NATURE METHODS, 2006, 3 (09) :696-700
[6]   Genomewide view of gene silencing by small interfering RNAs [J].
Chi, JT ;
Chang, HY ;
Wang, NN ;
Chang, DS ;
Dunphy, N ;
Brown, PO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (11) :6343-6346
[7]   No induction of anti-viral responses in human cell lines HeLa and MCF-7 when transfecting with siRNA or siLNA [J].
Dahlgren, C ;
Wahlestedt, C ;
Thonberg, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 341 (04) :1211-1217
[8]   A systematic analysis of the silencing effects of an active siRNA at all single-nucleotide mismatched target sites [J].
Du, Q ;
Thonberg, H ;
Wang, J ;
Wahlestedt, C ;
Liang, ZC .
NUCLEIC ACIDS RESEARCH, 2005, 33 (05) :1671-1677
[9]   Minimizing the risk of reporting false positives in large-scale RNAi screens [J].
Echeverri, Christophe J. ;
Beachy, Philip A. ;
Baum, Buzz ;
Boutros, Michael ;
Buchholz, Frank ;
Chanda, Sumit K. ;
Downward, Julian ;
Ellenberg, Jan ;
Fraser, Andrew G. ;
Hacohen, Nir ;
Hahn, William C. ;
Jackson, Aimee L. ;
Kiger, Amy ;
Linsley, Peter S. ;
Lum, Lawrence ;
Ma, Yong ;
Mathey-Prevot, Bernard ;
Root, David E. ;
Sabatini, David M. ;
Taipale, Jussi ;
Perrimon, Norbert ;
Bernards, Rene .
NATURE METHODS, 2006, 3 (10) :777-779
[10]   High-throughput RNAi screening in cultured cells: a user's guide [J].
Echeverri, CJ ;
Perrimon, N .
NATURE REVIEWS GENETICS, 2006, 7 (05) :373-384