Key result
An mRNA-bound proteome analysis in Trypanosoma brucei identified 155 high-confidence RNA-binding protein candidates, 27 of which affected reporter expression in a tethering screen.
The study identifies the mRNA-bound proteome in Trypanosoma brucei, revealing 155 high-confidence RNA-binding proteins and providing insights into post-transcriptional gene expression control.
Control of gene expression at the post-transcriptional level is essential in all organisms, and RNA-binding proteins play critical roles from mRNA synthesis to decay. To fully understand this process, it is necessary to identify the complete set of RNA-binding proteins and the functional consequences of the protein-mRNA interactions. Here, we provide an overview of the proteins that bind to mRNAs and their functions in the pathogenic bloodstream form of Trypanosoma brucei. We describe the production of a small collection of open-reading frames encoding proteins potentially involved in mRNA metabolism. With this ORFeome collection, we used tethering to screen for proteins that play a role in post-transcriptional control. A yeast two-hybrid screen showed that several of the discovered repressors interact with components of the CAF1/NOT1 deadenylation complex. To identify the RNA-binding proteins, we obtained the mRNA-bound proteome. We identified 155 high-confidence candidates, including many not previously annotated as RNA-binding proteins. Twenty seven of these proteins affected reporter expression in the tethering screen. Our study provides novel insights into the potential trypanosome mRNPs composition, architecture and function.
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Lueong et al. (2016) studied Trypanosoma brucei. mRNA-bound proteome analysis and tethering screen was evaluated on Identification of RNA-binding proteins and functional consequences. An mRNA-bound proteome analysis in Trypanosoma brucei identified 155 high-confidence RNA-binding protein candidates, 27 of which affected reporter expression in a tethering screen.
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