Počet záznamů: 1  

A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs

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    SYSNO ASEP0334100
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevA mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs
    Tvůrce(i) Huranová, Martina (UMG-J) ORCID
    Hnilicová, Jarmila (UMG-J)
    Fleischer, Branislav (UMG-J)
    Cvačková, Zuzana (UMG-J) RID
    Staněk, David (UMG-J) RID
    Celkový počet autorů5
    Zdroj.dok.Human Molecular Genetics. - : Oxford University Press - ISSN 0964-6906
    Roč. 18, č. 11 (2009), s. 2014-2023
    Poč.str.10 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovaretinitis pigmentosa ; snRNP ; splicing
    Vědní obor RIVEB - Genetika a molekulární biologie
    CEPKAN200520801 GA AV ČR - Akademie věd
    CEZAV0Z50520514 - UMG-J (2005-2011)
    UT WOS000265951600010
    DOI10.1093/hgm/ddp125
    AnotaceThe AD29 mutation in HPRP31 belongs to a series of mutations that were initially linked with the autosomal dominant disorder retinitis pigmentosa (RP) type 11. The HPRP31 gene encodes the hPrp31 protein that specifically associates with spliceosomal small nuclear ribonucleoprotein particles (snRNPs). In this study we report that expression of this mutant protein affects cell proliferation and alters the structure of nuclear Cajal bodies that are connected with snRNP metabolism. Interestingly, these effects can be reversed by the over-expression of the hPrp6 protein, a binding partner of hPrp31. We present several lines of evidence that demonstrate that association between the AD29 mutant and snRNPs in the cell nucleus is significantly reduced. Finally, we show that stability of the AD29 mutant is severely affected resulting in its rapid degradation. Taken together, our results significantly impact our understanding of the molecular mechanisms underlying RP.
    PracovištěÚstav molekulární genetiky
    KontaktNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Rok sběru2010
Počet záznamů: 1  

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