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Role of Inosine-Uracil Base Pairs in the Canonical RNA Duplexes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F18%3A00101215" target="_blank" >RIV/00216224:14740/18:00101215 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.3390/genes9070324" target="_blank" >http://dx.doi.org/10.3390/genes9070324</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/genes9070324" target="_blank" >10.3390/genes9070324</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Role of Inosine-Uracil Base Pairs in the Canonical RNA Duplexes

  • Original language description

    Adenosine to inosine (A-I) editing is the most common modification of double-stranded RNA (dsRNA). This change is mediated by adenosine deaminases acting on RNA (ADARs) enzymes with a preference of U&gt;A&gt;C&gt;G for 5' neighbor and G&gt;C=A&gt;U or G&gt;C&gt;U=A for 3' neighbor. A-I editing occurs most frequently in the non-coding regions containing repetitive elements such as ALUs. It leads to disruption of RNA duplex structure, which prevents induction of innate immune response. We employed standard and biased molecular dynamics (MD) simulations to analyze the behavior of RNA duplexes with single and tandem inosine-uracil (I-U) base pairs in different sequence context. Our analysis showed that the I-U pairs induce changes in base pair and base pair step parameters and have different dynamics when compared with standard canonical base pairs. In particular, the first I-U pair from tandem I-U/I-U systems exhibited increased dynamics depending on its neighboring 5' base. We discovered that UII sequence, which is frequently edited, has lower flexibility compared with other sequences (AII, GII, CII), hence it only modestly disrupts dsRNA. This might indicate that the UAA motifs in ALUs do not have to be sufficiently effective in preventing immune signaling.

  • 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

    30101 - Human genetics

Result continuities

  • Project

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

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    GENES

  • ISSN

    2073-4425

  • e-ISSN

  • Volume of the periodical

    9

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    14

  • Pages from-to

    324

  • UT code for WoS article

    000445149700011

  • EID of the result in the Scopus database

    2-s2.0-85049185757