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Nucleic Acids Research, 2003, Vol. 31, No. 7 e38
© 2003 Oxford University Press

A simple and cost-effective method for producing small interfering RNAs with high efficacy

Muhammad Sohail, Graeme Doran, Johann Riedemann1, Val Macaulay1 and Edwin M. Southern

University of Oxford, Department of Biochemistry, South Parks Road, Oxford OX1 3QU, UK and 1 Molecular Oncology Laboratory, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Headley Way, Headington, Oxford OX3 9DS, UK

*To whom correspondence should be addressed. Tel: +44 1865 275224; Fax: +44 1865 275259; Email: muhammad.sohail{at}bioch.ox.ac.uk

Small interfering RNAs (siRNAs) are powerful RNA interference (RNAi) reagents for directed post- transcriptional gene silencing. Exogenous siRNA is frequently used in RNAi studies. However, due to profound differences in the activity of siRNAs targeted to different regions of a gene, several reagents may have to be screened for optimal activity. This approach is expensive due to the cost of chemical synthesis of RNAs. We report a technically simple, quick and cost-effective method for the production of siRNAs that makes use of in vitro transcription and deoxyribozyme digestion of the transcripts to produce the desired sequence and length. The method allows for several siRNAs to be produced in parallel at much reduced costs. The siRNAs produced with this method were tested in MDA-MB-231 human breast cancer cells for efficacy against the type 1 insulin-like growth factor receptor (IGF1R) mRNA and they caused dose-dependent inhibition of IGF1R expression comparable to that induced by chemically synthesised siRNAs of the same sequence. This method is also useful for producing long RNA fragments of defined length and sequence that may be difficult to synthesise chemically, and also for producing large quantities of RNAs for applications including structural studies and the study of interactions between RNA and other molecules, such as proteins, other nucleic acids and drugs.


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