Key result
RNA interference of MRP1 and MRP2 in Trypanosoma brucei caused severe growth inhibition and transcript-specific editing changes, including a 5-fold increase in edited ND7 mRNA.
Mitochondrial RNA-binding proteins MRP1 and MRP2 play a transcript-specific regulatory role in RNA editing and processing in Trypanosoma brucei rather than being essential for the editing process itself.
Leaves open MRP1/2 as drug targets in trypanosomiasis; extends models of transcript-specific RNA editing in kinetoplastids.
Mitochondrial RNA-binding proteins MRP1 and MRP2 occur in a heteromeric complex that appears to play a role in U-insertion/deletion editing in trypanosomes. Reduction in the levels of MRP1 (gBP21) and/or MRP2 (gBP25) mRNA by RNA interference in procyclic Trypanosoma brucei resulted in severe growth inhibition. It also resulted in the loss of both proteins, even when only one of the MRP mRNAs was reduced, indicating a mutual dependence for stability. Elimination of the MRPs gave rise to substantially reduced levels of edited CyB and RPS12 mRNAs but little or no reduction of the level of edited Cox2, Cox3, and A6 mRNAs as measured by poisoned primer extension analyses. In contrast, edited NADH-dehydrogenase (ND) subunit 7 mRNA was increased 5-fold in MRP1+2 double knock-down cells. Furthermore, MRP elimination resulted in reduced levels of Cox1, ND4, and ND5 mRNAs, which are never edited, whereas mitoribosomal 12 S rRNA levels were not affected. These data indicate that MRP1 and MRP2 are not essential for RNA editing per se but, rather, play a regulatory role in the editing of specific transcripts and other RNA processing activities.
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Vondrušková et al. (2004) studied this question. RNA interference of MRP1 and/or MRP2 was evaluated on Levels of edited and unedited mitochondrial mRNAs. RNA interference of MRP1 and MRP2 in Trypanosoma brucei caused severe growth inhibition and transcript-specific editing changes, including a 5-fold increase in edited ND7 mRNA.
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