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SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes

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    0520462 - BC 2020 RIV US eng J - Journal Article
    Saura, A. - Iribarren, P.A. - Rojas-Barros, D. - Bart, J.M. - Lopez-Farfan, D. - Andres-Leon, E. - Vidal-Cobo, I. - Boehm, C. - Alvarez, V.E. - Field, Mark Christian - Navarro, M.
    SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes.
    Embo Reports. NOV 2019, NOV 2019 (2019), č. článku e48029. ISSN 1469-221X. E-ISSN 1469-3178
    Institutional support: RVO:60077344
    Keywords : i transcription factor * epigenetic regulation * gene-expression * phd finger * domain * sites * proliferation * architecture * quiescence * mechanisms * antigenic variation * plant homeodomain * post-translational modification * sumo * variant surface glycoprotein
    OECD category: Biochemistry and molecular biology
    Impact factor: 7.497, year: 2019
    Method of publishing: Open access
    https://www.embopress.org/doi/pdf/10.15252/embr.201948029

    SUMOylation is a post-translational modification that positively regulates monoallelic expression of the trypanosome variant surface glycoprotein (VSG). The presence of a highly SUMOylated focus associated with the nuclear body, where the VSG gene is transcribed, further suggests an important role of SUMOylation in regulating VSG expression. Here, we show that SNF2PH, a SUMOylated plant homeodomain (PH)-transcription factor, is upregulated in the bloodstream form of the parasite and enriched at the active VSG telomere. SUMOylation promotes the recruitment of SNF2PH to the VSG promoter, where it is required to maintain RNA polymerase I and thus to regulate VSG transcript levels. Further, ectopic overexpression of SNF2PH in insect forms, but not of a mutant lacking the PH domain, induces the expression of bloodstream stage-specific surface proteins. These data suggest that SNF2PH SUMOylation positively regulates VSG monoallelic transcription, while the PH domain is required for the expression of bloodstream-specific surface proteins. Thus, SNF2PH functions as a positive activator, linking expression of infective form surface proteins and VSG regulation, thereby acting as a major regulator of pathogenicity.
    Permanent Link: http://hdl.handle.net/11104/0305130

     
     
Number of the records: 1  

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