Evidence map›Paper›PMID 39099254›Full record

ArticleMolecular biology and evolution2024

Complex Genomes of Early Nucleocytoviruses Revealed by Ancient Origins of Viral Aminoacyl-tRNA Synthetases.

Soichiro Kijima, Hiroyuki Hikida, Tom O Delmont, Morgan Gaïa, Hiroyuki Ogata

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Soichiro KijimaChemical Life Science, Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.ORCID 0009-0006-3272-9391
Hiroyuki HikidaChemical Life Science, Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.ORCID 0000-0002-4876-3133
Tom O DelmontGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ. Evry, Université Paris-Saclay, 91057 Evry, France.ORCID 0000-0001-7053-7848
Morgan GaïaGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ. Evry, Université Paris-Saclay, 91057 Evry, France.ORCID 0000-0003-4936-4780
Hiroyuki OgataChemical Life Science, Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan.ORCID 0000-0001-6594-377X

Funding

Japan Society for the Promotion of Science KAKENHI 22H00384Kyoto University Research Coordination AllianceResearch Unit for Development of Global SustainabilityWellcome Trust 202332
6 · The paper itself

Abstract

Aminoacyl-tRNA synthetases (aaRSs), also known as tRNA ligases, are essential enzymes in translation. Owing to their functional essentiality, these enzymes are conserved in all domains of life and used as informative markers to trace the evolutionary history of cellular organisms. Unlike cellular organisms, viruses generally lack aaRSs because of their obligate parasitic nature, but several large and giant DNA viruses in the phylum Nucleocytoviricota encode aaRSs in their genomes. The discovery of viral aaRSs led to the idea that the phylogenetic analysis of aaRSs can shed light on ancient viral evolution. However, conflicting results have been reported from previous phylogenetic studies: one posited that nucleocytoviruses recently acquired their aaRSs from their host eukaryotes, while another hypothesized that the viral aaRSs have ancient origins. Here, we investigated 4,168 nucleocytovirus genomes, including metagenome-assembled genomes (MAGs) derived from large-scale metagenomic studies. In total, we identified 780 viral aaRS sequences in 273 viral genomes. We generated and examined phylogenetic trees of these aaRSs with a large set of cellular sequences to trace evolutionary relationships between viral and cellular aaRSs. The analyses suggest that the origins of some viral aaRSs predate the last common eukaryotic ancestor. Inside viral aaRS clades, we identify intricate evolutionary trajectories of viral aaRSs with horizontal transfers, losses, and displacements. Overall, these results suggest that ancestral nucleocytoviruses already developed complex genomes with an expanded set of aaRSs in the proto-eukaryotic era.

Indexed as

Amino Acyl-tRNA SynthetasesEvolution, MolecularGenome, ViralPhylogenyDNA VirusesAmino Acyl-tRNA Synthetasesaminoacyl-tRNA synthetaseancestral originNucleocytoviricota

Identifiers

PMID39099254
PMCPMC11304981

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