HAL will be down for maintenance from Friday, June 10 at 4pm through Monday, June 13 at 9am. More information
Skip to Main content Skip to Navigation
Journal articles

Towards Understanding Human Mitochondrial Leucine Aminoacylation Identity

Abstract : Specific recognition of tRNAs by aminoacyl-tRNA synthetases is governed by sets of aminoacylation identity elements, well defined for numerous prokaryotic systems and eukaryotic cytosolic systems. Only restricted information is available for aminoacylation of human mito-chondrial tRNAs, despite their particularities linked to the non-classical structures of the tRNAs and their involvement in a growing number of human neurodegenerative disorders linked to mutations in the corresponding tRNA genes. A major difficulty to be overcome is the preparation of active in vitro transcripts enabling a rational mutagenic analysis, as is currently performed for classical tRNAs. Here, structural and aminoacylation properties of in vitro transcribed tRNA Leu(UUR) are presented. Solution probing using a combination of enzymatic and chemical tools revealed only partial folding into an L-shaped structure, with an acceptor branch but with a floppy anticodon branch. Optimization of aminoacylation conditions allowed charging of up to 75% of molecules, showing that, despite its partially relaxed structure, in vitro transcribed tRNA Leu(UUR) is able to adapt to the synthetase. In addition, mutational analysis demonstrates that the discriminator base as well as residue A14 are important leucine identity elements. Thus, human mitochondrial leucylation is dependent on rules similar to those that apply in Escherichia coli. The impact of a subset of pathology-related mutations on amino-acylation and on tRNA structure, has been explored. These variants do not show significant structural rearrangements and either do not affect aminoacylation (mutations T3250C, T3271C, C3303T) or lead to marked effects. Interestingly, two variants with a mutation at the same position (A3243G and A3243T) lead to markedly different losses in aminoacylation efficiencies (tenfold and 300-fold, respectively).
Document type :
Journal articles
Complete list of metadata

Contributor : Bénédicte Sohm Connect in order to contact the contributor
Submitted on : Tuesday, April 2, 2019 - 4:33:46 PM
Last modification on : Tuesday, May 10, 2022 - 3:38:03 PM

Links full text



Bénédicte Sohm, Magali Frugier, Hervé Brulé, Krzysztof Olszak, Anna Przykorska, et al.. Towards Understanding Human Mitochondrial Leucine Aminoacylation Identity. Journal of Molecular Biology, Elsevier, 2003, ⟨10.1016/S0022-2836(03)00373-5⟩. ⟨hal-02088226⟩



Record views