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Enhanced RNAi does not provide efficient innate antiviral immunity in mice

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F25%3A00642229" target="_blank" >RIV/60077344:_____/25:00642229 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/25:00642229 RIV/60076658:12310/25:43909734 RIV/00216224:14310/25:00140568 RIV/00027162:_____/25:N0000012

  • Result on the web

    <a href="https://academic.oup.com/nar/article/53/1/gkae1288/7945392" target="_blank" >https://academic.oup.com/nar/article/53/1/gkae1288/7945392</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/nar/gkae1288" target="_blank" >10.1093/nar/gkae1288</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Enhanced RNAi does not provide efficient innate antiviral immunity in mice

  • Original language description

    In RNA interference (RNAi), long double-stranded RNA is cleaved by the Dicer endonuclease into small interfering RNAs (siRNAs), which guide degradation of complementary RNAs. While RNAi mediates antiviral innate immunity in plants and many invertebrates, vertebrates have adopted a sequence-independent response and their Dicer produces siRNAs inefficiently because it is adapted to process small hairpin microRNA precursors in the gene-regulating microRNA pathway. Mammalian endogenous RNAi is thus a rudimentary pathway of unclear significance. To investigate its antiviral potential, we modified the mouse Dicer locus to express a truncated variant (Dicer ΔHEL1 ) known to stimulate RNAi and we analyzed how Dicer ΔHEL1/wt mice respond to four RNA viruses: coxsackievirus B3 and encephalomyocarditis virus from Picornaviridae, tick-borne encephalitis virus from Flaviviridae, and lymphocytic choriomeningitis virus (LCMV) from Arenaviridae. Increased Dicer activity in Dicer ΔHEL1/wt mice did not elicit any antiviral effect, supporting an insignificant antiviral function of endogenous mammalian RNAi in vivo. However, we also observed that sufficiently high expression of DicerΔHEL1 suppressed LCMV in embryonic stem cells and in a transgenic mouse model. Altogether, mice with increased Dicer activity offer a new benchmark for identifying and studying viruses susceptible to mammalian RNAi in vivo.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10607 - Virology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • 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

    1362-4962

  • Volume of the periodical

    53

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    18

  • Pages from-to

    gkae1288

  • UT code for WoS article

    001391535800001

  • EID of the result in the Scopus database

    2-s2.0-85214572319