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dsRNA expression in the mouse elicits RNAi in oocytes and low adenosine deamination in somatic cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F12%3A00371756" target="_blank" >RIV/68378050:_____/12:00371756 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1093/nar/gkr702" target="_blank" >http://dx.doi.org/10.1093/nar/gkr702</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/nar/gkr702" target="_blank" >10.1093/nar/gkr702</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    dsRNA expression in the mouse elicits RNAi in oocytes and low adenosine deamination in somatic cells

  • Original language description

    Double-stranded RNA (dsRNA) can enter sequence-specific RNA interference (RNAi), sequence-independent interferon (IFN) response and editing by adenosine deaminases pathways. To study the fate of dsRNA in vivo, we used transgenic mice ubiquitously expressing from a promoter an mRNA with a long hairpin. The expressed dsRNA did not cause any developmental defects nor activated the IFN response, which was inducible only at high expression levels in cultured cells. dsRNA was poorly processed into siRNAs in somatic cells while 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 an edited small fraction of long dsRNA. RNA editing did not prevent 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.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA204%2F09%2F0085" target="_blank" >GA204/09/0085: RNA silencing and long dsRNA in mammalian cells</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2012

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Nucleic Acids Research

  • ISSN

    0305-1048

  • e-ISSN

  • Volume of the periodical

    40

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    15

  • Pages from-to

    399-413

  • UT code for WoS article

    000298733500043

  • EID of the result in the Scopus database