Evolutionary rate analysis of aminoacyl tRNA synthetases
Data files
Aug 02, 2023 version files 85.96 KB
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20221206_orthogroups_geneID.csv
1.46 KB
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alignments_pretrimmed.zip
34.26 KB
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cytosolic.zip
29.26 KB
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organellar.zip
19.03 KB
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README.md
1.94 KB
Abstract
Eukaryotic nuclear genomes often encode distinct sets of protein translation machinery for function in the cytosol vs. organelles (mitochondria and plastids). This phenomenon raises questions about why multiple translation systems are maintained even though they are capable of comparable functions, and whether they evolve differently depending on the compartment where they operate. These questions are particularly interesting in land plants because translation machinery, including aminoacyl-tRNA synthetases (aaRS), is often dual-targeted to both the plastids and mitochondria. These two organelles have quite different metabolisms, with much higher rates of translation in plastids to supply the abundant, rapid-turnover proteins required for photosynthesis. Previous studies have indicated that plant organellar aaRS evolve more slowly compared to mitochondrial aaRS in other eukaryotes that lack plastids. Thus, we investigated the evolution of nuclear-encoded organellar and cytosolic translation machinery across a broad sampling of angiosperms, including non-photosynthetic (heterotrophic) plant species with reduced rates of plastid gene expression to test the hypothesis that translational demands associated with photosynthesis constrain the evolution of bacterial-like enzymes involved in organellar tRNA metabolism. Remarkably, heterotrophic plants exhibited wholesale loss of many organelle-targeted aaRS and other enzymes, even though translation still occurs in their mitochondria and plastids. These losses were often accompanied by apparent retargeting of cytosolic enzymes and tRNAs to the organelles, sometimes preserving aaRS-tRNA charging relationships but other times creating surprising mismatches between cytosolic aaRS and mitochondrial tRNA substrates. Our findings indicate that the presence of a photosynthetic plastid drives the retention of specialized systems for organellar tRNA metabolism.
Datasets are multiple sequence alignments and gene trees for aminoacyl tRNA-synthetase enzyme amino acid sequences curated from publically available data. These data were used to evaluate evolutionary rate. I've also included code used for analysis.
Python3
Jupyter Notebooks
MEGA11
- DeTar, Rachael (2023), Finding orthologs for aminoacyl tRNA synthetases in parasitic plants, , Dataset, https://doi.org/10.5061/dryad.0cfxpnw7p
- DeTar, Rachael (2023), In silico subcellular targeting predictions for cytosolic aminoacyl tRNA-synthetases (aaRS) in parasitic plants, , Dataset, https://doi.org/10.5061/dryad.6hdr7sr5x
- DeTar, Rachael (2023), Organellar tRNAs in parasitic plant species, , Dataset, https://doi.org/10.5061/dryad.np5hqc009
- DeTar, Rachael Ann et al. (2023), Photosynthesis drives retention of bacterial-like tRNA metabolism in plant organelles, [], Posted-content, https://doi.org/10.1101/2023.08.01.551541
- DeTar, Rachael (2023), Evolutionary rate analysis of aminoacyl tRNA synthetases, , Article, https://doi.org/10.5281/zenodo.8185160
- DeTar, Rachael A.; Chustecki, Joanna M.; Martinez-Hottovy, Ana et al. (2024). Photosynthetic demands on translational machinery drive retention of redundant tRNA metabolism in plant organelles. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.2421485121
