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DNA polymerase diversity reveals multiple incursions of Polintons during nematode evolution
Open accessPreprint — published as 10.1093/molbev/msad274
Abstract
Polintons are dsDNA, virus-like self-synthesizing transposons widely found in eukaryotic genomes. Recent metagenomic discoveries of Polinton-like viruses are consistent with the hypothesis that Polintons invade eukaryotic host genomes through infectious viral particles. Nematode genomes contain multiple copies of Polintons and provide an opportunity to explore the natural distribution and evolution of Polintons during this process. We performed an extensive search of Polintons across nematode genomes, identifying multiple full-length Polinton copies in several species. We provide evidence of both ancient Polinton integrations and recent mobility in strains of the same nematode species. In addition to the major nematode Polinton family, we identified a group of Polintons that are overall closely related to the major family, but encode a distinct protein-primed B family DNA polymerase (pPolB) that is related to homologs from a different group of Polintons present outside of the Nematoda . Phylogenetic analyses on the pPolBs support the evolutionary scenarios in which these extrinsic pPolBs that seem to derive from Polinton families present in oomycetes and molluscs replaced the canonical pPolB in subsets of Polintons found in terrestrial and marine nematodes, respectively, suggesting inter-phylum horizontal gene transfers. The pPolBs of the terrestrial nematode and oomycete Polintons share a unique feature, an insertion of a HNH nuclease domain, whereas the pPolBs in the marine nematode Polintons share an insertion of a VSR nuclease domain with marine mollusc pPolBs. We hypothesize that horizontal gene transfer occurs among Polintons from widely different but cohabiting hosts.
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Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
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Metadata
- Authors
- Jeong, D.-E., Sundrani, S., Hall, R. N., Krupovic, M., Koonin, E. V., & Fire, A. Z.
- Affiliations
- Stanford Medicine (US)
- Vanderbilt University (US)
- Stanford University (US)
- National Institutes of Health (US)
- Corresponding author
- Jeong, Dae-Eun
- Fire, Andrew Z.
- ORCID
- Venue
- Molecular Biology and Evolution
- Publisher
- openRxiv
- Published
- 2023-08-23
- Volume
- 40
- Issue
- 12
- Pages
- msad274
- ISSN
- 0737-4038 (ISSN-L)
- PMC
- PMC10748475
- OpenAlex
- W4389525192
- Cited by
- 12
- References
- 1
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 4
- FWCI
- 1.89
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by-nc
- Locations
- Molecular Biology and Evolution (publishedVersion, cc-by-nc)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- HAL (submittedVersion, cc-by-nc)
- PubMed Central (submittedVersion)
- Funders
- Human Frontier Science Program (LT000329/2019-L)
- National Institutes of Health
- School of Medicine, Stanford University
- National Institute of General Medical Sciences (R35GM130366)
- U.S. National Library of Medicine (ZIALM000073)
- Stanford Cardiovascular Institute, School of Medicine, Stanford University
- Intramural Research Program
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Nematode management and characterization studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- DNA polymerase B, nematode genome, transposon evolution, horizontal gene transfer, Polinton-like viruses, oomycete, Mollusca, transposon mobility, nematode evolution
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