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Depletion of the RNA-Binding Protein RBP33 Results in Increased Expression of Silenced RNA Polymerase II Transcripts in Trypanosoma brucei
Author(s) -
Sandra M. FernándezMoya,
Mark Carrington,
Antonio M. Estévez
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0107608
Subject(s) - biology , rna , trypanosoma brucei , rna binding protein , rna induced silencing complex , small nuclear rna , microbiology and biotechnology , non coding rna , rna polymerase iii , immunoprecipitation , gene expression , gene , genetics , rna polymerase
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.

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