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CpG-creating mutations are costly in many human viruses

Mutations can occur throughout the virus genome and may be beneficial, neutral or deleterious. We are interested in mutations that yield a C next to a G, producing CpG sites. CpG sites are rare in eukaryotic and viral genomes. For the eukaryotes, it is thought that CpG sites are rare because they ar...

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Autores principales: Caudill, Victoria R., Qin, Sarina, Winstead, Ryan, Kaur, Jasmeen, Tisthammer, Kaho, Pineda, E. Geo, Solis, Caroline, Cobey, Sarah, Bedford, Trevor, Carja, Oana, Eggo, Rosalind M., Koelle, Katia, Lythgoe, Katrina, Regoes, Roland, Roy, Scott, Allen, Nicole, Aviles, Milo, Baker, Brittany A., Bauer, William, Bermudez, Shannel, Carlson, Corey, Castellanos, Edgar, Catalan, Francisca L., Chemel, Angeline Katia, Elliot, Jacob, Evans, Dwayne, Fiutek, Natalie, Fryer, Emily, Goodfellow, Samuel Melvin, Hecht, Mordecai, Hopp, Kellen, Hopson, E. Deshawn, Jaberi, Amirhossein, Kinney, Christen, Lao, Derek, Le, Adrienne, Lo, Jacky, Lopez, Alejandro G., López, Andrea, Lorenzo, Fernando G., Luu, Gordon T., Mahoney, Andrew R., Melton, Rebecca L., Nascimento, Gabriela Do, Pradhananga, Anjani, Rodrigues, Nicole S., Shieh, Annie, Sims, Jasmine, Singh, Rima, Sulaeman, Hasan, Thu, Ricky, Tran, Krystal, Tran, Livia, Winters, Elizabeth J., Wong, Albert, Pennings, Pleuni S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245597/
https://www.ncbi.nlm.nih.gov/pubmed/32508375
http://dx.doi.org/10.1007/s10682-020-10039-z
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author Caudill, Victoria R.
Qin, Sarina
Winstead, Ryan
Kaur, Jasmeen
Tisthammer, Kaho
Pineda, E. Geo
Solis, Caroline
Cobey, Sarah
Bedford, Trevor
Carja, Oana
Eggo, Rosalind M.
Koelle, Katia
Lythgoe, Katrina
Regoes, Roland
Roy, Scott
Allen, Nicole
Aviles, Milo
Baker, Brittany A.
Bauer, William
Bermudez, Shannel
Carlson, Corey
Castellanos, Edgar
Catalan, Francisca L.
Chemel, Angeline Katia
Elliot, Jacob
Evans, Dwayne
Fiutek, Natalie
Fryer, Emily
Goodfellow, Samuel Melvin
Hecht, Mordecai
Hopp, Kellen
Hopson, E. Deshawn
Jaberi, Amirhossein
Kinney, Christen
Lao, Derek
Le, Adrienne
Lo, Jacky
Lopez, Alejandro G.
López, Andrea
Lorenzo, Fernando G.
Luu, Gordon T.
Mahoney, Andrew R.
Melton, Rebecca L.
Nascimento, Gabriela Do
Pradhananga, Anjani
Rodrigues, Nicole S.
Shieh, Annie
Sims, Jasmine
Singh, Rima
Sulaeman, Hasan
Thu, Ricky
Tran, Krystal
Tran, Livia
Winters, Elizabeth J.
Wong, Albert
Pennings, Pleuni S.
author_facet Caudill, Victoria R.
Qin, Sarina
Winstead, Ryan
Kaur, Jasmeen
Tisthammer, Kaho
Pineda, E. Geo
Solis, Caroline
Cobey, Sarah
Bedford, Trevor
Carja, Oana
Eggo, Rosalind M.
Koelle, Katia
Lythgoe, Katrina
Regoes, Roland
Roy, Scott
Allen, Nicole
Aviles, Milo
Baker, Brittany A.
Bauer, William
Bermudez, Shannel
Carlson, Corey
Castellanos, Edgar
Catalan, Francisca L.
Chemel, Angeline Katia
Elliot, Jacob
Evans, Dwayne
Fiutek, Natalie
Fryer, Emily
Goodfellow, Samuel Melvin
Hecht, Mordecai
Hopp, Kellen
Hopson, E. Deshawn
Jaberi, Amirhossein
Kinney, Christen
Lao, Derek
Le, Adrienne
Lo, Jacky
Lopez, Alejandro G.
López, Andrea
Lorenzo, Fernando G.
Luu, Gordon T.
Mahoney, Andrew R.
Melton, Rebecca L.
Nascimento, Gabriela Do
Pradhananga, Anjani
Rodrigues, Nicole S.
Shieh, Annie
Sims, Jasmine
Singh, Rima
Sulaeman, Hasan
Thu, Ricky
Tran, Krystal
Tran, Livia
Winters, Elizabeth J.
Wong, Albert
Pennings, Pleuni S.
author_sort Caudill, Victoria R.
collection PubMed
description Mutations can occur throughout the virus genome and may be beneficial, neutral or deleterious. We are interested in mutations that yield a C next to a G, producing CpG sites. CpG sites are rare in eukaryotic and viral genomes. For the eukaryotes, it is thought that CpG sites are rare because they are prone to mutation when methylated. In viruses, we know less about why CpG sites are rare. A previous study in HIV suggested that CpG-creating transition mutations are more costly than similar non-CpG-creating mutations. To determine if this is the case in other viruses, we analyzed the allele frequencies of CpG-creating and non-CpG-creating mutations across various strains, subtypes, and genes of viruses using existing data obtained from Genbank, HIV Databases, and Virus Pathogen Resource. Our results suggest that CpG sites are indeed costly for most viruses. By understanding the cost of CpG sites, we can obtain further insights into the evolution and adaptation of viruses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10682-020-10039-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-72455972020-06-03 CpG-creating mutations are costly in many human viruses Caudill, Victoria R. Qin, Sarina Winstead, Ryan Kaur, Jasmeen Tisthammer, Kaho Pineda, E. Geo Solis, Caroline Cobey, Sarah Bedford, Trevor Carja, Oana Eggo, Rosalind M. Koelle, Katia Lythgoe, Katrina Regoes, Roland Roy, Scott Allen, Nicole Aviles, Milo Baker, Brittany A. Bauer, William Bermudez, Shannel Carlson, Corey Castellanos, Edgar Catalan, Francisca L. Chemel, Angeline Katia Elliot, Jacob Evans, Dwayne Fiutek, Natalie Fryer, Emily Goodfellow, Samuel Melvin Hecht, Mordecai Hopp, Kellen Hopson, E. Deshawn Jaberi, Amirhossein Kinney, Christen Lao, Derek Le, Adrienne Lo, Jacky Lopez, Alejandro G. López, Andrea Lorenzo, Fernando G. Luu, Gordon T. Mahoney, Andrew R. Melton, Rebecca L. Nascimento, Gabriela Do Pradhananga, Anjani Rodrigues, Nicole S. Shieh, Annie Sims, Jasmine Singh, Rima Sulaeman, Hasan Thu, Ricky Tran, Krystal Tran, Livia Winters, Elizabeth J. Wong, Albert Pennings, Pleuni S. Evol Ecol Original Paper Mutations can occur throughout the virus genome and may be beneficial, neutral or deleterious. We are interested in mutations that yield a C next to a G, producing CpG sites. CpG sites are rare in eukaryotic and viral genomes. For the eukaryotes, it is thought that CpG sites are rare because they are prone to mutation when methylated. In viruses, we know less about why CpG sites are rare. A previous study in HIV suggested that CpG-creating transition mutations are more costly than similar non-CpG-creating mutations. To determine if this is the case in other viruses, we analyzed the allele frequencies of CpG-creating and non-CpG-creating mutations across various strains, subtypes, and genes of viruses using existing data obtained from Genbank, HIV Databases, and Virus Pathogen Resource. Our results suggest that CpG sites are indeed costly for most viruses. By understanding the cost of CpG sites, we can obtain further insights into the evolution and adaptation of viruses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10682-020-10039-z) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-04-24 2020 /pmc/articles/PMC7245597/ /pubmed/32508375 http://dx.doi.org/10.1007/s10682-020-10039-z Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Caudill, Victoria R.
Qin, Sarina
Winstead, Ryan
Kaur, Jasmeen
Tisthammer, Kaho
Pineda, E. Geo
Solis, Caroline
Cobey, Sarah
Bedford, Trevor
Carja, Oana
Eggo, Rosalind M.
Koelle, Katia
Lythgoe, Katrina
Regoes, Roland
Roy, Scott
Allen, Nicole
Aviles, Milo
Baker, Brittany A.
Bauer, William
Bermudez, Shannel
Carlson, Corey
Castellanos, Edgar
Catalan, Francisca L.
Chemel, Angeline Katia
Elliot, Jacob
Evans, Dwayne
Fiutek, Natalie
Fryer, Emily
Goodfellow, Samuel Melvin
Hecht, Mordecai
Hopp, Kellen
Hopson, E. Deshawn
Jaberi, Amirhossein
Kinney, Christen
Lao, Derek
Le, Adrienne
Lo, Jacky
Lopez, Alejandro G.
López, Andrea
Lorenzo, Fernando G.
Luu, Gordon T.
Mahoney, Andrew R.
Melton, Rebecca L.
Nascimento, Gabriela Do
Pradhananga, Anjani
Rodrigues, Nicole S.
Shieh, Annie
Sims, Jasmine
Singh, Rima
Sulaeman, Hasan
Thu, Ricky
Tran, Krystal
Tran, Livia
Winters, Elizabeth J.
Wong, Albert
Pennings, Pleuni S.
CpG-creating mutations are costly in many human viruses
title CpG-creating mutations are costly in many human viruses
title_full CpG-creating mutations are costly in many human viruses
title_fullStr CpG-creating mutations are costly in many human viruses
title_full_unstemmed CpG-creating mutations are costly in many human viruses
title_short CpG-creating mutations are costly in many human viruses
title_sort cpg-creating mutations are costly in many human viruses
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7245597/
https://www.ncbi.nlm.nih.gov/pubmed/32508375
http://dx.doi.org/10.1007/s10682-020-10039-z
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