The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Unexpected Inheritance: Multiple Integrations of Ancient Bornavirus and Ebolavirus/Marburgvirus Sequences in Vertebrate Genomes
Open accessAbstract
Vertebrate genomes contain numerous copies of retroviral sequences, acquired over the course of evolution. Until recently they were thought to be the only type of RNA viruses to be so represented, because integration of a DNA copy of their genome is required for their replication. In this study, an extensive sequence comparison was conducted in which 5,666 viral genes from all known non-retroviral families with single-stranded RNA genomes were matched against the germline genomes of 48 vertebrate species, to determine if such viruses could also contribute to the vertebrate genetic heritage. In 19 of the tested vertebrate species, we discovered as many as 80 high-confidence examples of genomic DNA sequences that appear to be derived, as long ago as 40 million years, from ancestral members of 4 currently circulating virus families with single strand RNA genomes. Surprisingly, almost all of the sequences are related to only two families in the Order Mononegavirales: the Bornaviruses and the Filoviruses, which cause lethal neurological disease and hemorrhagic fevers, respectively. Based on signature landmarks some, and perhaps all, of the endogenous virus-like DNA sequences appear to be LINE element-facilitated integrations derived from viral mRNAs. The integrations represent genes that encode viral nucleocapsid, RNA-dependent-RNA-polymerase, matrix and, possibly, glycoproteins. Integrations are generally limited to one or very few copies of a related viral gene per species, suggesting that once the initial germline integration was obtained (or selected), later integrations failed or provided little advantage to the host. The conservation of relatively long open reading frames for several of the endogenous sequences, the virus-like protein regions represented, and a potential correlation between their presence and a species' resistance to the diseases caused by these pathogens, are consistent with the notion that their products provide some important biological advantage to the species. In addition, the viruses could also benefit, as some resistant species (e.g. bats) may serve as natural reservoirs for their persistence and transmission. Given the stringent limitations imposed in this informatics search, the examples described here should be considered a low estimate of the number of such integration events that have persisted over evolutionary time scales. Clearly, the sources of genetic information in vertebrate genomes are much more diverse than previously suspected.
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A gene atlas of the mouse and human protein-encoding transcriptomes
Su, A. I., Wiltshire, T., Batalov, S., Lapp, H., Ching, K. A., Block, D., Zhang, J., Soden, R., Hayakawa, M., Kreiman, G., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400782101 · Cited by 3,475
The sequence and de novo assembly of the giant panda genome
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West Nile Virus: A Reemerging Global Pathogen
Petersen, L. R., & Roehrig, J. T. (2001) · Emerging Infectious Diseases · doi:10.3201/eid0704.017401 · Cited by 435
Rates of Nucleotide Substitution in Primates and Rodents and the Generation–Time Effect Hypothesis
Li, W.-H., Ellsworth, D. L., Krushkal, J., Chang, B. H.-J., & Hewett-Emmett, D. (1996) · Molecular Phylogenetics and Evolution · doi:10.1006/mpev.1996.0012 · Cited by 335 · cited 1×
“12% of nucleotides per million years in primates to 2–4 times that value in rodents [13,14,15,16].”
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Cited by
Endogenous viruses: insights into viral evolution and impact on host biology
Feschotte, C., & Gilbert, C. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3199 · Cited by 891
RELAX: Detecting Relaxed Selection in a Phylogenetic Framework
Wertheim, J. O., Murrell, B., Smith, M. D., Kosakovsky Pond, S. L., & Scheffler, K. (2015) · Molecular Biology and Evolution · doi:10.1093/molbev/msu400 · Cited by 778
Bats host major mammalian paramyxoviruses
Drexler, J. F., Corman, V. M., Müller, M. A., Maganga, G. D., Vallo, P., Binger, T., Gloza-Rausch, F., Cottontail, V. M., Rasche, A., Yordanov, S., et al. (2012) · Nature Communications · doi:10.1038/ncomms1796 · Cited by 686
Rules of engagement: molecular insights from host–virus arms races
Daugherty, M. D., & Malik, H. S. (2012) · Annual Review of Genetics · doi:10.1146/annurev-genet-110711-155522 · Cited by 515
Discovery of an Ebolavirus-Like Filovirus in Europe
Negredo, A., Palacios, G., Vázquez-Morón, S., González, F., Dopazo, H., Molero, F., Juste, J., Quetglas, J., Savji, N., de la Cruz Martínez, M., et al. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002304 · Cited by 431
Metadata
- Authors
- Belyi, V. A., Levine, A. J., & Skalka, A. M.
- Venue
- PLoS Pathogens
- Publisher
- Public Library of Science (PLoS)
- Published
- 2010-07-29
- Volume
- 6
- Issue
- 7
- Pages
- e1001030
- ISSN
- 1553-7366 (ISSN-L)
- 1553-7374
- OpenAlex
- W2170430743
- Cited by
- 292
- References
- 4
- FWCI
- 29.83
- Type
- journal article
- Language
- en
- Open access
- gold
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- Belyi, V. A., Levine, A. J., & Skalka, A. M. (2010). Unexpected Inheritance: Multiple Integrations of Ancient Bornavirus and Ebolavirus/Marburgvirus Sequences in Vertebrate Genomes. PLoS Pathogens. https://doi.org/10.1371/journal.ppat.1001030
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