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BRF1, a subunit of RNA polymerase III transcription factor TFIIIB, is essential for cell growth of Trypanosoma brucei
- VÉLEZ-RAMÍREZ, D. E., FLORENCIO-MARTÍNEZ, L. E., ROMERO-MEZA, G., ROJAS-SÁNCHEZ, S., MORENO-CAMPOS, R., ARROYO, R., ORTEGA-LÓPEZ, J., MANNING-CELA, R., MARTÍNEZ-CALVILLO, S.
- Parasitology 2015 v.142 no.13 pp. 1563-1573
- DNA-directed RNA polymerase, RNA, RNA interference, Trypanosoma brucei, cell growth, cell viability, cyclins, genes, models, parasites, procyclic forms, quantitative polymerase chain reaction, transcription factors, zinc
- RNA polymerase III (Pol III) synthesizes small RNA molecules that are essential for cell viability. Accurate initiation of transcription by Pol III requires general transcription factor TFIIIB, which is composed of three subunits: TFIIB-related factor BRF1, TATA-binding protein and BDP1. Here we report the molecular characterization of BRF1 in Trypanosoma brucei (TbBRF1), a parasitic protozoa that shows distinctive transcription characteristics. In silico analysis allowed the detection in TbBRF1 of the three conserved domains located in the N-terminal region of all BRF1 orthologues, namely a zinc ribbon motif and two cyclin repeats. Homology modelling suggested that, similarly to other BRF1 and TFIIB proteins, the TbBRF1 cyclin repeats show the characteristic structure of five α-helices per repeat, connected by a short random-coiled linker. As expected for a transcription factor, TbBRF1 was localized in the nucleus. Knock-down of TbBRF1 by RNA interference (RNAi) showed that this protein is essential for the viability of procyclic forms of T. brucei, since ablation of TbBRF1 led to growth arrest of the parasites. Nuclear run-on and quantitative real-time PCR analyses demonstrated that transcription of all the Pol III-dependent genes analysed was reduced, at different levels, after RNAi induction.