Evolutionary genomics of nucleo-cytoplasmic large DNA viruses - PubMed
Review
. 2006 Apr;117(1):156-84.
doi: 10.1016/j.virusres.2006.01.009. Epub 2006 Feb 21.
Affiliations
- PMID: 16494962
- DOI: 10.1016/j.virusres.2006.01.009
Review
Evolutionary genomics of nucleo-cytoplasmic large DNA viruses
Lakshminarayan M Iyer et al. Virus Res. 2006 Apr.
Abstract
A previous comparative-genomic study of large nuclear and cytoplasmic DNA viruses (NCLDVs) of eukaryotes revealed the monophyletic origin of four viral families: poxviruses, asfarviruses, iridoviruses, and phycodnaviruses [Iyer, L.M., Aravind, L., Koonin, E.V., 2001. Common origin of four diverse families of large eukaryotic DNA viruses. J. Virol. 75 (23), 11720-11734]. Here we update this analysis by including the recently sequenced giant genome of the mimiviruses and several additional genomes of iridoviruses, phycodnaviruses, and poxviruses. The parsimonious reconstruction of the gene complement of the ancestral NCLDV shows that it was a complex virus with at least 41 genes that encoded the replication machinery, up to four RNA polymerase subunits, at least three transcription factors, capping and polyadenylation enzymes, the DNA packaging apparatus, and structural components of an icosahedral capsid and the viral membrane. The phylogeny of the NCLDVs is reconstructed by cladistic analysis of the viral gene complements, and it is shown that the two principal lineages of NCLDVs are comprised of poxviruses grouped with asfarviruses and iridoviruses grouped with phycodnaviruses-mimiviruses. The phycodna-mimivirus grouping was strongly supported by several derived shared characters, which seemed to rule out the previously suggested basal position of the mimivirus [Raoult, D., Audic, S., Robert, C., Abergel, C., Renesto, P., Ogata, H., La Scola, B., Suzan, M., Claverie, J.M. 2004. The 1.2-megabase genome sequence of Mimivirus. Science 306 (5700), 1344-1350]. These results indicate that the divergence of the major NCLDV families occurred at an early stage of evolution, prior to the divergence of the major eukaryotic lineages. It is shown that subsequent evolution of the NCLDV genomes involved lineage-specific expansion of paralogous gene families and acquisition of numerous genes via horizontal gene transfer from the eukaryotic hosts, other viruses, and bacteria (primarily, endosymbionts and parasites). Amongst the expansions, there are multiple families of predicted virus-specific signaling and regulatory domains. Most NCLDVs have also acquired large arrays of genes related to ubiquitin signaling, and the animal viruses in particular have independently evolved several defenses against apoptosis and immune response, including growth factors and potential inhibitors of cytokine signaling. The mimivirus displays an enormous array of genes of bacterial provenance, including a representative of a new class of predicted papain-like peptidases. It is further demonstrated that a significant number of genes found in NCLDVs also have homologs in bacteriophages, although a vertical relationship between the NCLDVs and a particular bacteriophage group could not be established. On the basis of these observations, two alternative scenarios for the origin of the NCLDVs and other groups of large DNA viruses of eukaryotes are considered. One of these scenarios posits an early assembly of an already large DNA virus precursor from which various large DNA viruses diverged through an ongoing process of displacement of the original genes by xenologous or non-orthologous genes from various sources. The second scenario posits convergent emergence, on multiple occasions, of large DNA viruses from small plasmid-like precursors through independent accretion of similar sets of genes due to strong selective pressures imposed by their life cycles and hosts.
Similar articles
-
Common origin of four diverse families of large eukaryotic DNA viruses.
Iyer LM, Aravind L, Koonin EV. Iyer LM, et al. J Virol. 2001 Dec;75(23):11720-34. doi: 10.1128/JVI.75.23.11720-11734.2001. J Virol. 2001. PMID: 11689653 Free PMC article.
-
Yutin N, Wolf YI, Raoult D, Koonin EV. Yutin N, et al. Virol J. 2009 Dec 17;6:223. doi: 10.1186/1743-422X-6-223. Virol J. 2009. PMID: 20017929 Free PMC article.
-
Yutin N, Koonin EV. Yutin N, et al. Biol Direct. 2009 Dec 18;4:51. doi: 10.1186/1745-6150-4-51. Biol Direct. 2009. PMID: 20021668 Free PMC article.
-
Filée J. Filée J. J Invertebr Pathol. 2009 Jul;101(3):169-71. doi: 10.1016/j.jip.2009.03.010. Epub 2009 May 18. J Invertebr Pathol. 2009. PMID: 19457437 Review.
-
Koonin EV, Yutin N. Koonin EV, et al. Adv Virus Res. 2019;103:167-202. doi: 10.1016/bs.aivir.2018.09.002. Epub 2018 Nov 10. Adv Virus Res. 2019. PMID: 30635076 Review.
Cited by
-
Efficiency in Complexity: Composition and Dynamic Nature of Mimivirus Replication Factories.
Fridmann-Sirkis Y, Milrot E, Mutsafi Y, Ben-Dor S, Levin Y, Savidor A, Kartvelishvily E, Minsky A. Fridmann-Sirkis Y, et al. J Virol. 2016 Oct 14;90(21):10039-10047. doi: 10.1128/JVI.01319-16. Print 2016 Nov 1. J Virol. 2016. PMID: 27581975 Free PMC article.
-
Urbano AC, Ferreira F. Urbano AC, et al. Vaccines (Basel). 2020 Oct 3;8(4):585. doi: 10.3390/vaccines8040585. Vaccines (Basel). 2020. PMID: 33023005 Free PMC article. Review.
-
The evolutionary biology of poxviruses.
Hughes AL, Irausquin S, Friedman R. Hughes AL, et al. Infect Genet Evol. 2010 Jan;10(1):50-9. doi: 10.1016/j.meegid.2009.10.001. Epub 2009 Oct 13. Infect Genet Evol. 2010. PMID: 19833230 Free PMC article. Review.
-
Moreau H, Piganeau G, Desdevises Y, Cooke R, Derelle E, Grimsley N. Moreau H, et al. J Virol. 2010 Dec;84(24):12555-63. doi: 10.1128/JVI.01123-10. Epub 2010 Sep 22. J Virol. 2010. PMID: 20861243 Free PMC article.
-
Ogata H, Toyoda K, Tomaru Y, Nakayama N, Shirai Y, Claverie JM, Nagasaki K. Ogata H, et al. Virol J. 2009 Oct 27;6:178. doi: 10.1186/1743-422X-6-178. Virol J. 2009. PMID: 19860921 Free PMC article.