Abstract
Mitochondrial polycistronic transcripts are extensively processed to give rise to functional mRNAs, rRNAs and tRNAs; starting with the release of tRNA elements through 5-processing by RNase P (MRPP1/2/3-complex) and 3-processing by RNase Z (ELAC2). Here, we show using in vitro experiments that MRPP1/2 is not only a component of the mitochondrial RNase P but that it retains the tRNA product from the 5-processing step and significantly enhances the efficiency of ELAC2-catalyzed 3-processing for 17 of the 22 tRNAs encoded in the human mitochondrial genome. Furthermore, MRPP1/2 retains the tRNA product after ELAC2 processing and presents the nascent tRNA to the mitochondrial CCA-Adding enzyme. Thus, in addition to being an essential component of the RNase P reaction, MRPP1/2 serves as a processing platform for several down-stream tRNA maturation steps in human mitochondria. These findings are of fundamental importance for our molecular understanding of disease-related mutations in MRPP1/2, ELAC2 and mitochondrial tRNA genes.
Cite
CITATION STYLE
Reinhard, L., Sridhara, S., & Hällberg, B. M. (2017). The MRPP1/MRPP2 complex is a tRNA-maturation platform in human mitochondria. Nucleic Acids Research, 45(21), 12469–12480. https://doi.org/10.1093/nar/gkx902
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.