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RNA processing in human mitochondria.

by: Maria Lopez I. Sanchez, Tim R. Mercer, Stefan M. Davies, Anne-Marie M. Shearwood, Karoline K. Nygård, Tara R. Richman, John S. Mattick, Oliver Rackham, Aleksandra Filipovska
Cell cycle (Georgetown, Tex.), Vol. 10, No. 17. (1 September 2011), pp. 2904-2916  Key: citeulike:9938675

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Abstract

Mammalian mitochondrial DNA is transcribed as precursor polycistronic transcripts containing 13 mRNAs, 2 rRNAs, punctuated by 22 tRNAs. The mechanisms involved in the excision of mitochondrial tRNAs from these polycistronic transcripts have remained largely unknown. We have investigated the roles of ELAC2, mitochondrial RNase P proteins 1 and 3, and pentatricopeptide repeat domain protein 1 in the processing of mitochondrial polycistronic transcripts. We used a deep sequencing approach to characterize the 5' and 3' ends of processed mitochondrial transcripts and provide a detailed map of mitochondrial tRNA processing sites affected by these proteins. We show that MRPP1 and MRPP3 process the 5' ends of tRNAs and the 5' unconventional, non tRNA containing site of the CO1 transcript. By contrast, we find that ELAC2 and PTCD1 affect the 3' end processing of tRNAs. Finally, we found that MRPP1 is essential for transcript processing, RNA modification, translation and mitochondrial respiration. © 2011 Landes Bioscience


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