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Genome rearrangement affects RNA virus adaptability on prostate cancer cells
Gene order is often highly conserved within taxonomic groups, such that organisms with rearranged genomes tend to be less fit than wild type gene orders, and suggesting natural selection favors genome architectures that maximize fitness. But it is unclear whether rearranged genomes hinder adaptabili...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381649/ https://www.ncbi.nlm.nih.gov/pubmed/25883601 http://dx.doi.org/10.3389/fgene.2015.00121 |
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author | Pesko, Kendra Voigt, Emily A. Swick, Adam Morley, Valerie J. Timm, Collin Yin, John Turner, Paul E. |
author_facet | Pesko, Kendra Voigt, Emily A. Swick, Adam Morley, Valerie J. Timm, Collin Yin, John Turner, Paul E. |
author_sort | Pesko, Kendra |
collection | PubMed |
description | Gene order is often highly conserved within taxonomic groups, such that organisms with rearranged genomes tend to be less fit than wild type gene orders, and suggesting natural selection favors genome architectures that maximize fitness. But it is unclear whether rearranged genomes hinder adaptability: capacity to evolutionarily improve in a new environment. Negative-sense non-segmented RNA viruses (order Mononegavirales) have specific genome architecture: 3′ UTR – core protein genes – envelope protein genes – RNA-dependent RNA-polymerase gene – 5′ UTR. To test how genome architecture affects RNA virus evolution, we examined vesicular stomatitis virus (VSV) variants with the nucleocapsid (N) gene moved sequentially downstream in the genome. Because RNA polymerase stuttering in VSV replication causes greater mRNA production in upstream genes, N gene translocation toward the 5′ end leads to stepwise decreases in N transcription, viral replication and progeny production, and also impacts the activation of type 1 interferon mediated antiviral responses. We evolved VSV gene-order variants in two prostate cancer cell lines: LNCap cells deficient in innate immune response to viral infection, and PC-3 cells that mount an IFN stimulated anti-viral response to infection. We observed that gene order affects phenotypic adaptability (reproductive growth; viral suppression of immune function), especially on PC-3 cells that strongly select against virus infection. Overall, populations derived from the least-fit ancestor (most-altered N position architecture) adapted fastest, consistent with theory predicting populations with low initial fitness should improve faster in evolutionary time. Also, we observed correlated responses to selection, where viruses improved across both hosts, rather than suffer fitness trade-offs on unselected hosts. Whole genomics revealed multiple mutations in evolved variants, some of which were conserved across selective environments for a given gene order. |
format | Online Article Text |
id | pubmed-4381649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43816492015-04-16 Genome rearrangement affects RNA virus adaptability on prostate cancer cells Pesko, Kendra Voigt, Emily A. Swick, Adam Morley, Valerie J. Timm, Collin Yin, John Turner, Paul E. Front Genet Genetics Gene order is often highly conserved within taxonomic groups, such that organisms with rearranged genomes tend to be less fit than wild type gene orders, and suggesting natural selection favors genome architectures that maximize fitness. But it is unclear whether rearranged genomes hinder adaptability: capacity to evolutionarily improve in a new environment. Negative-sense non-segmented RNA viruses (order Mononegavirales) have specific genome architecture: 3′ UTR – core protein genes – envelope protein genes – RNA-dependent RNA-polymerase gene – 5′ UTR. To test how genome architecture affects RNA virus evolution, we examined vesicular stomatitis virus (VSV) variants with the nucleocapsid (N) gene moved sequentially downstream in the genome. Because RNA polymerase stuttering in VSV replication causes greater mRNA production in upstream genes, N gene translocation toward the 5′ end leads to stepwise decreases in N transcription, viral replication and progeny production, and also impacts the activation of type 1 interferon mediated antiviral responses. We evolved VSV gene-order variants in two prostate cancer cell lines: LNCap cells deficient in innate immune response to viral infection, and PC-3 cells that mount an IFN stimulated anti-viral response to infection. We observed that gene order affects phenotypic adaptability (reproductive growth; viral suppression of immune function), especially on PC-3 cells that strongly select against virus infection. Overall, populations derived from the least-fit ancestor (most-altered N position architecture) adapted fastest, consistent with theory predicting populations with low initial fitness should improve faster in evolutionary time. Also, we observed correlated responses to selection, where viruses improved across both hosts, rather than suffer fitness trade-offs on unselected hosts. Whole genomics revealed multiple mutations in evolved variants, some of which were conserved across selective environments for a given gene order. Frontiers Media S.A. 2015-04-01 /pmc/articles/PMC4381649/ /pubmed/25883601 http://dx.doi.org/10.3389/fgene.2015.00121 Text en Copyright © 2015 Pesko, Voigt, Swick, Morley, Timm, Yin and Turner. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Pesko, Kendra Voigt, Emily A. Swick, Adam Morley, Valerie J. Timm, Collin Yin, John Turner, Paul E. Genome rearrangement affects RNA virus adaptability on prostate cancer cells |
title | Genome rearrangement affects RNA virus adaptability on prostate cancer cells |
title_full | Genome rearrangement affects RNA virus adaptability on prostate cancer cells |
title_fullStr | Genome rearrangement affects RNA virus adaptability on prostate cancer cells |
title_full_unstemmed | Genome rearrangement affects RNA virus adaptability on prostate cancer cells |
title_short | Genome rearrangement affects RNA virus adaptability on prostate cancer cells |
title_sort | genome rearrangement affects rna virus adaptability on prostate cancer cells |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381649/ https://www.ncbi.nlm.nih.gov/pubmed/25883601 http://dx.doi.org/10.3389/fgene.2015.00121 |
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