The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Nidovirales: Evolving the largest RNA virus genome
Open accessAbstract
This review focuses on the monophyletic group of animal RNA viruses united in the order Nidovirales. The order includes the distantly related coronaviruses, toroviruses, and roniviruses, which possess the largest known RNA genomes (from 26 to 32 kb) and will therefore be called ‘large’ nidoviruses in this review. They are compared with their arterivirus cousins, which also belong to the Nidovirales despite having a much smaller genome (13–16 kb). Common and unique features that have been identified for either large or all nidoviruses are outlined. These include the nidovirus genetic plan and genome diversity, the composition of the replicase machinery and virus particles, virus-specific accessory genes, the mechanisms of RNA and protein synthesis, and the origin and evolution of nidoviruses with small and large genomes. Nidoviruses employ single-stranded, polycistronic RNA genomes of positive polarity that direct the synthesis of the subunits of the replicative complex, including the RNA-dependent RNA polymerase and helicase. Replicase gene expression is under the principal control of a ribosomal frameshifting signal and a chymotrypsin-like protease, which is assisted by one or more papain-like proteases. A nested set of subgenomic RNAs is synthesized to express the 3′-proximal ORFs that encode most conserved structural proteins and, in some large nidoviruses, also diverse accessory proteins that may promote virus adaptation to specific hosts. The replicase machinery includes a set of RNA-processing enzymes some of which are unique for either all or large nidoviruses. The acquisition of these enzymes may have improved the low fidelity of RNA replication to allow genome expansion and give rise to the ancestors of small and, subsequently, large nidoviruses.
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Cites
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Cited by
Neurologic alterations due to respiratory virus infections
Bohmwald, K., Gálvez, N. M. S., Ríos, M., & Kalergis, A. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00386 · Cited by 636
“It has been described that non-structural proteins are the leading cause of host immune system modulation and they also play a role in the replication of the genetic material of the virus (Gorbalenya et al., 2006).”
BackgroundContinuous and Discontinuous RNA Synthesis in Coronaviruses
Sola, I., Almazán, F., Zúñiga, S., & Enjuanes, L. (2015) · Annual Review of Virology · doi:10.1146/annurev-virology-100114-055218 · Cited by 643
Self-citationIn Vitro Reconstitution of SARS-Coronavirus mRNA Cap Methylation
Bouvet, M., Debarnot, C., Imbert, I., Selisko, B., Snijder, E. J., Canard, B., & Decroly, E. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000863 · Cited by 406
Self-citationOudshoorn, D., Rijs, K., Limpens, R. W. A. L., Groen, K., Koster, A. J., Snijder, E. J., Kikkert, M., & Bárcena, M. (2017) · mBio · doi:10.1128/mbio.01658-17 · Cited by 245
Self-citationProteomics Analysis Unravels the Functional Repertoire of Coronavirus Nonstructural Protein 3
Neuman, B. W., Joseph, J. S., Saikatendu, K. S., Serrano, P., Chatterjee, A., Johnson, M. A., Liao, L., Klaus, J. P., Yates, J. R., Wüthrich, K., et al. (2008) · Journal of Virology · doi:10.1128/jvi.02631-07 · Cited by 192
Metadata
- Authors
- Gorbalenya, A. E., Enjuanes, L., Ziebuhr, J., & Snijder, E. J.
- Venue
- Virus Research
- Publisher
- Elsevier BV
- Published
- 2006-04
- Volume
- 117
- Issue
- 1
- Pages
- 17-37
- ISSN
- 0168-1702 (ISSN-L)
- OpenAlex
- W1971168306
- Cited by
- 922
- References
- 4
- FWCI
- 57.76
- Type
- journal article
- Language
- en
- Open access
- green
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