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- W2013960131 abstract "Double-stranded RNA (dsRNA) can enter different pathways in mammalian cells, including sequence-specific RNA interference (RNAi), sequence-independent interferon (IFN) response and editing by adenosine deaminases. To study the routing of dsRNA to these pathways in vivo, we used transgenic mice ubiquitously expressing from a strong promoter, an mRNA with a long hairpin in its 3′-UTR. The expressed dsRNA neither caused any developmental defects nor activated the IFN response, which was inducible only at high expression levels in cultured cells. The dsRNA was poorly processed into siRNAs in somatic cells, whereas, robust RNAi effects were found in oocytes, suggesting that somatic cells lack some factor(s) facilitating siRNA biogenesis. Expressed dsRNA did not cause transcriptional silencing in trans. Analysis of RNA editing revealed that a small fraction of long dsRNA is edited. RNA editing neither prevented the cytoplasmic localization nor processing into siRNAs. Thus, a long dsRNA structure is well tolerated in mammalian cells and is mainly causing a robust RNAi response in oocytes." @default.
- W2013960131 created "2016-06-24" @default.
- W2013960131 creator A5001819361 @default.
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- W2013960131 creator A5060049750 @default.
- W2013960131 creator A5069584240 @default.
- W2013960131 creator A5072989236 @default.
- W2013960131 date "2011-09-08" @default.
- W2013960131 modified "2023-10-01" @default.
- W2013960131 title "dsRNA expression in the mouse elicits RNAi in oocytes and low adenosine deamination in somatic cells" @default.
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- W2013960131 doi "https://doi.org/10.1093/nar/gkr702" @default.
- W2013960131 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3245926" @default.
- W2013960131 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21908396" @default.
- W2013960131 hasPublicationYear "2011" @default.
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