Released selective pressure on a structural domain gives new insights on the functional relaxation of mitochondrial aspartyl-tRNA synthetase

• Published in: Biochimie 2014-05, Vol.100, p.18-26
• Main Authors: Schwenzer, Hagen, Scheper, Gert C, Zorn, Nathalie, Moulinier, Luc, Gaudry, Agnès, Leize, Emmanuelle, Martin, Franck, Florentz, Catherine, Poch, Olivier, Sissler, Marie
• Format: Article
• Language: English
• Subjects: Alternative Splicing; Alveolata - enzymology; Alveolata - genetics; Amino Acid Sequence; Amoebozoa - enzymology; Amoebozoa - genetics; Animals; Archaea - enzymology; Archaea - genetics; Aspartate-tRNA Ligase - chemistry; Aspartate-tRNA Ligase - genetics; Aspartate-tRNA Ligase - metabolism; Base Sequence; Biochemistry, Molecular Biology; Evolution, Molecular; Fungi - enzymology; Fungi - genetics; Gene Expression; Humans; Life Sciences; Mitochondria - enzymology; Mitochondria - genetics; Mitochondrial Proteins - chemistry; Mitochondrial Proteins - genetics; Mitochondrial Proteins - metabolism; Models, Molecular; Molecular Sequence Data; Mutagenesis, Insertional; Protein Biosynthesis; Protein Structure, Tertiary; RNA, Messenger - chemistry; RNA, Messenger - genetics; RNA, Messenger - metabolism; Selection, Genetic; Sequence Alignment; Viridiplantae - enzymology; Viridiplantae - genetics
• ISSN: 0300-9084; 1638-6183
• DOI: 10.1016/j.biochi.2013.09.027

Mammalian mitochondrial aminoacyl-tRNA synthetases are nuclear-encoded enzymes that are essential for mitochondrial protein synthesis. Due to an endosymbiotic origin of the mitochondria, many of them share structural domains with homologous bacterial enzymes of same specificity. This is also the case for human mitochondrial aspartyl-tRNA synthetase (AspRS) that shares the so-called bacterial insertion domain with bacterial homologs. The function of this domain in the mitochondrial proteins is unclear. Here, we show by bioinformatic analyses that the sequences coding for the bacterial insertion domain are less conserved in opisthokont and protist than in bacteria and viridiplantae. The divergence suggests a loss of evolutionary pressure on this domain for non-plant mitochondrial AspRSs. This discovery is further connected with the herein described occurrence of alternatively spliced transcripts of the mRNAs coding for some mammalian mitochondrial AspRSs. Interestingly, the spliced transcripts alternately lack one of the four exons that code for the bacterial insertion domain. Although we showed that the human alternative transcript is present in all tested tissues; co-exists with the full-length form, possesses 5'- and 3'-UTRs, a poly-A tail and is bound to polysomes, we were unable to detect the corresponding protein. The relaxed selective pressure combined with the occurrence of alternative splicing, involving a single structural sub-domain, favors the hypothesis of the loss of function of this domain for AspRSs of mitochondrial location. This evolutionary divergence is in line with other characteristics, established for the human mt-AspRS, that indicate a functional relaxation of non-viridiplantae mt-AspRSs when compared to bacterial and plant ones, despite their common ancestry.