Suppression of the Sendai Virus M Protein through a Novel Short Interfering RNA Approach Inhibits Viral Particle Production but Does Not Affect Viral RNA Synthesis
Author(s) -
Geneviève Mottet-Osman,
Frédéric Iseni,
Thierry Pelet,
Maciej Wiznerowicz,
Dominique Garcin,
Laurent Roux
Publication year - 2006
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.02291-06
Subject(s) - sendai virus , biology , rna interference , transcription (linguistics) , viral replication , small interfering rna , rna , microbiology and biotechnology , gene silencing , dna directed rna interference , rna silencing , virology , protein biosynthesis , rna induced silencing complex , messenger rna , untranslated region , virus , gene , genetics , linguistics , philosophy
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.
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