SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
203134/Z/16/Z
Wellcome Trust - United Kingdom
RTI2018-098834-B-I00
Ministerio de Ciencia, Innovación y Universidades - International
Wellcome Trust - United Kingdom
WTI 204697/Z/16/Z
Wellcome Trust - United Kingdom
PICT-2016-0465
Argentinian National Agency for Promotion of Scientific and Technological Research - International
PubMed
31693280
PubMed Central
PMC6893287
DOI
10.15252/embr.201948029
Knihovny.cz E-zdroje
- Klíčová slova
- SUMO, antigenic variation, plant homeodomain, post-translational modification, variant surface glycoprotein,
- MeSH
- epigeneze genetická MeSH
- glykoproteiny genetika metabolismus MeSH
- protozoální proteiny genetika metabolismus MeSH
- restrukturace chromatinu MeSH
- RNA-polymerasa I metabolismus MeSH
- sumoylace * MeSH
- transkripční faktory genetika metabolismus MeSH
- Trypanosoma brucei brucei genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- glykoproteiny MeSH
- protozoální proteiny MeSH
- RNA-polymerasa I MeSH
- transkripční faktory MeSH
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.
Biology Centre Institute of Parasitology Czech Academy of Sciences Ceske Budejovice Czech Republic
IIB UNSAM Buenos Aires Argentina
Instituto de Parasitología y Biomedicina López Neyra CSIC Granada Spain
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A hub-and-spoke nuclear lamina architecture in trypanosomes
SRA
PRJNA562785