Depletion of the RNA-binding protein RBP33 results in increased expression of silenced RNA polymerase II transcripts in trypanosoma brucei
Publication date
2014ISSN
1932-6203
Abstract
We have characterized the RNA-binding protein RBP33 in Trypanosoma brucei, and found that it localizes to the nucleus and is essential for viability. The subset of RNAs bound to RBP33 was determined by immunoprecipitation of ribonucleoprotein complexes followed by deep sequencing. Most RBP33-bound transcripts are predicted to be non-coding. Among these, over one-third are located close to the end of transcriptional units (TUs) or have an antisense orientation within a TU. Depletion of RBP33 resulted in an increase in the level of RNAs derived from regions that are normally silenced, such as strand-switch regions, retroposon and repeat sequences. Our work provides the first example of an RNA-binding protein involved in the regulation of gene silencing in trypanosomes.
Document Type
Article
Document version
Published version
Language
English
Subject (CDU)
61 - Medical sciences
Pages
7
Publisher
PLOS
Collection
9; 9
Is part of
PLOS One
Recommended citation
Fernández-Moya, Sandra M.; Carrington, Mark; Estévez, Antonio M. [et al.]. Depletion of the RNA-binding protein RBP33 results in increased expression of silenced RNA polymerase II transcripts in trypanosoma brucei. PLOS One, 2014, 9(9), e107608. Disponible en: <https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0107608>. Fecha de acceso: 24 ene. 2025. DOI: 10.1371/journal.pone.0107608
Note
AME was funded by Spanish Plan Nacional, grant BFU 2009-07510. MC was funded by The Wellcome Trust, grant 085956/Z/08/Z. AME and MC were jointly funded by the Royal Society Joint Project grant, grant 2008/R2. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
This item appears in the following Collection(s)
- Ciències de la Salut [980]
Rights
© 2014 Fernández-Moya et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/

