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Dual targeting is the rule for organellar aminoacyl-tRNA synthetases in Arabidopsis thaliana
Author(s) -
AnneMarie Duchêne,
Anatoli Giritch,
Beate Hoffmann,
Valérie Cognat,
Dominique Lancelin,
Nemo Peeters,
Marlyse Zaepfel,
Laurence MaréchalDrouard,
Ian Small
Publication year - 2005
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0504682102
Subject(s) - aminoacyl trna synthetase , plastid , mitochondrion , biology , arabidopsis thaliana , transfer rna , cytosol , chloroplast , arabidopsis , gene , amino acyl trna synthetases , protein biosynthesis , translation (biology) , compartment (ship) , nuclear gene , genome , genetics , microbiology and biotechnology , biochemistry , rna , enzyme , messenger rna , oceanography , mutant , geology
In plants, protein synthesis occurs in the cytosol, mitochondria, and plastids. Each compartment requires a full set of tRNAs and aminoacyl-tRNA synthetases. We have undertaken a systematic analysis of the targeting of organellar aminoacyl-tRNA synthetases in the model plant Arabidopsis thaliana. Dual targeting appeared to be a general rule. Among the 24 identified organellar aminoacyl-tRNA synthetases (aaRSs), 15 (and probably 17) are shared between mitochondria and plastids, and 5 are shared between cytosol and mitochondria (one of these aaRSs being present also in chloroplasts). Only two were shown to be uniquely chloroplastic and none to be uniquely mitochondrial. Moreover, there are no examples where the three aaRS genes originating from the three ancestral genomes still coexist. These results indicate that extensive exchange of aaRSs has occurred during evolution and that many are now shared between two or even three compartments. The findings have important implications for studies of the translation machinery in plants and on protein targeting and gene transfer in general.

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