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Journal of Virology, March 2007, p. 2861-2868, Vol. 81, No. 6
0022-538X/07/$08.00+0 doi:10.1128/JVI.02291-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Department of Microbiology and Molecular Medicine, University of Geneva Medical School, CMU, 1 Rue Michel-Servet, CH-1211 Geneva 4, Switzerland,1 Swiss Federal Institute of Technology, School of Life Sciences, CH-1015 Lausanne, Switzerland,2 Centre de Recherche du Service de Santé des Armées, 24 Avenue des Maquis du Grésivaudan, F-38702, La Tronche, France3
Received 19 October 2006/ Accepted 14 December 2006
Short RNA interference is more and more widely recognized as an effective method to specifically suppress viral functions in eukaryotic cells. Here, we used an experimental system that allows suppression of the Sendai virus (SeV) M protein by using a target sequence, derived from the green fluorescent protein gene, that was introduced in the 3' untranslated region of the M protein mRNA. Silencing of the M protein gene was eventually achieved by a small interfering RNA (siRNA) directed against this target sequence. This siRNA was constitutively expressed in a cell line constructed by transduction with an appropriate lentivirus vector. Suppression of the M protein was sufficient to diminish virus production by 50- to 100-fold. This level of suppression had no apparent effect on viral replication and transcription, supporting the lack of M involvement in SeV transcription or replication control.
Published ahead of print on 27 December 2006.
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