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Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses

Numerous metagenomic studies have uncovered a remarkable diversity of circular replication-associated protein (Rep)-encoding single-stranded (CRESS) DNA viruses, the majority of which are uncultured and unclassified. Unlike capsid proteins, the Reps show significant similarity across different group...

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Autores principales: Kazlauskas, Darius, Varsani, Arvind, Krupovic, Mart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923481/
https://www.ncbi.nlm.nih.gov/pubmed/29642587
http://dx.doi.org/10.3390/v10040187
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author Kazlauskas, Darius
Varsani, Arvind
Krupovic, Mart
author_facet Kazlauskas, Darius
Varsani, Arvind
Krupovic, Mart
author_sort Kazlauskas, Darius
collection PubMed
description Numerous metagenomic studies have uncovered a remarkable diversity of circular replication-associated protein (Rep)-encoding single-stranded (CRESS) DNA viruses, the majority of which are uncultured and unclassified. Unlike capsid proteins, the Reps show significant similarity across different groups of CRESS DNA viruses and have conserved domain organization with the N-terminal nuclease and the C-terminal helicase domain. Consequently, Rep is widely used as a marker for identification, classification and assessment of the diversity of CRESS DNA viruses. However, it has been shown that in certain viruses the Rep nuclease and helicase domains display incongruent evolutionary histories. Here, we systematically evaluated the co-evolutionary patterns of the two Rep domains across classified and unclassified CRESS DNA viruses. Our analysis indicates that the Reps encoded by members of the families Bacilladnaviridae, Circoviridae, Geminiviridae, Genomoviridae, Nanoviridae and Smacoviridae display largely congruent evolutionary patterns in the two domains. By contrast, among the unclassified CRESS DNA viruses, 71% appear to have chimeric Reps. Such massive chimerism suggests that unclassified CRESS DNA viruses represent a dynamic population in which exchange of gene fragments encoding the nuclease and helicase domains is extremely common. Furthermore, purging of the chimeric sequences uncovered six monophyletic Rep groups that may represent new families of CRESS DNA viruses.
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spelling pubmed-59234812018-05-03 Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses Kazlauskas, Darius Varsani, Arvind Krupovic, Mart Viruses Article Numerous metagenomic studies have uncovered a remarkable diversity of circular replication-associated protein (Rep)-encoding single-stranded (CRESS) DNA viruses, the majority of which are uncultured and unclassified. Unlike capsid proteins, the Reps show significant similarity across different groups of CRESS DNA viruses and have conserved domain organization with the N-terminal nuclease and the C-terminal helicase domain. Consequently, Rep is widely used as a marker for identification, classification and assessment of the diversity of CRESS DNA viruses. However, it has been shown that in certain viruses the Rep nuclease and helicase domains display incongruent evolutionary histories. Here, we systematically evaluated the co-evolutionary patterns of the two Rep domains across classified and unclassified CRESS DNA viruses. Our analysis indicates that the Reps encoded by members of the families Bacilladnaviridae, Circoviridae, Geminiviridae, Genomoviridae, Nanoviridae and Smacoviridae display largely congruent evolutionary patterns in the two domains. By contrast, among the unclassified CRESS DNA viruses, 71% appear to have chimeric Reps. Such massive chimerism suggests that unclassified CRESS DNA viruses represent a dynamic population in which exchange of gene fragments encoding the nuclease and helicase domains is extremely common. Furthermore, purging of the chimeric sequences uncovered six monophyletic Rep groups that may represent new families of CRESS DNA viruses. MDPI 2018-04-10 /pmc/articles/PMC5923481/ /pubmed/29642587 http://dx.doi.org/10.3390/v10040187 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kazlauskas, Darius
Varsani, Arvind
Krupovic, Mart
Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses
title Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses
title_full Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses
title_fullStr Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses
title_full_unstemmed Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses
title_short Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses
title_sort pervasive chimerism in the replication-associated proteins of uncultured single-stranded dna viruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923481/
https://www.ncbi.nlm.nih.gov/pubmed/29642587
http://dx.doi.org/10.3390/v10040187
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