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SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes
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 o...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893287/ https://www.ncbi.nlm.nih.gov/pubmed/31693280 http://dx.doi.org/10.15252/embr.201948029 |
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author | Saura, Andreu Iribarren, Paula A Rojas‐Barros, Domingo Bart, Jean M López‐Farfán, Diana Andrés‐León, Eduardo Vidal‐Cobo, Isabel Boehm, Cordula Alvarez, Vanina E Field, Mark C Navarro, Miguel |
author_facet | Saura, Andreu Iribarren, Paula A Rojas‐Barros, Domingo Bart, Jean M López‐Farfán, Diana Andrés‐León, Eduardo Vidal‐Cobo, Isabel Boehm, Cordula Alvarez, Vanina E Field, Mark C Navarro, Miguel |
author_sort | Saura, Andreu |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6893287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68932872019-12-16 SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes Saura, Andreu Iribarren, Paula A Rojas‐Barros, Domingo Bart, Jean M López‐Farfán, Diana Andrés‐León, Eduardo Vidal‐Cobo, Isabel Boehm, Cordula Alvarez, Vanina E Field, Mark C Navarro, Miguel EMBO Rep Articles 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. John Wiley and Sons Inc. 2019-11-06 2019-12-05 /pmc/articles/PMC6893287/ /pubmed/31693280 http://dx.doi.org/10.15252/embr.201948029 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Saura, Andreu Iribarren, Paula A Rojas‐Barros, Domingo Bart, Jean M López‐Farfán, Diana Andrés‐León, Eduardo Vidal‐Cobo, Isabel Boehm, Cordula Alvarez, Vanina E Field, Mark C Navarro, Miguel SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes |
title | SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes |
title_full | SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes |
title_fullStr | SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes |
title_full_unstemmed | SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes |
title_short | SUMOylated SNF2PH promotes variant surface glycoprotein expression in bloodstream trypanosomes |
title_sort | sumoylated snf2ph promotes variant surface glycoprotein expression in bloodstream trypanosomes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893287/ https://www.ncbi.nlm.nih.gov/pubmed/31693280 http://dx.doi.org/10.15252/embr.201948029 |
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