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Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis

Identification of retrotransposon insertions in nonmodel taxa can be technically challenging and costly. This has inhibited progress in understanding retrotransposon insertion dynamics outside of a few well-studied species. To address this problem, we have extended a retrotransposon-based capture an...

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Autores principales: Platt, Roy N., Zhang, Yuhua, Witherspoon, David J., Xing, Jinchuan, Suh, Alexander, Keith, Megan S., Jorde, Lynn B., Stevens, Richard D., Ray, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494050/
https://www.ncbi.nlm.nih.gov/pubmed/26014613
http://dx.doi.org/10.1093/gbe/evv099
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author Platt, Roy N.
Zhang, Yuhua
Witherspoon, David J.
Xing, Jinchuan
Suh, Alexander
Keith, Megan S.
Jorde, Lynn B.
Stevens, Richard D.
Ray, David A.
author_facet Platt, Roy N.
Zhang, Yuhua
Witherspoon, David J.
Xing, Jinchuan
Suh, Alexander
Keith, Megan S.
Jorde, Lynn B.
Stevens, Richard D.
Ray, David A.
author_sort Platt, Roy N.
collection PubMed
description Identification of retrotransposon insertions in nonmodel taxa can be technically challenging and costly. This has inhibited progress in understanding retrotransposon insertion dynamics outside of a few well-studied species. To address this problem, we have extended a retrotransposon-based capture and sequence method (ME-Scan [mobile element scanning]) to identify insertions belonging to the Ves family of short interspersed elements (SINEs) across seven species of the bat genus Myotis. We identified between 120,000 and 143,000 SINE insertions in six taxa lacking a draft genome by comparing to the M. lucifugus reference genome. On average, each Ves insertion was sequenced to 129.6 × coverage. When mapped back to the M. lucifugus reference genome, all insertions were confidently assigned within a 10-bp window. Polymorphic Ves insertions were identified in each taxon based on their mapped locations. Using cross-species comparisons and the identified insertion positions, a presence–absence matrix was created for approximately 796,000 insertions. Dollo parsimony analysis of more than 85,000 phylogenetically informative insertions recovered strongly supported, monophyletic clades that correspond with the biogeography of each taxa. This phylogeny is similar to previously published mitochondrial phylogenies, with the exception of the placement of M. vivesi. These results support the utility of our variation on ME-Scan to identify polymorphic retrotransposon insertions in taxa without a reference genome and for large-scale retrotransposon-based phylogenetics.
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spelling pubmed-44940502015-07-09 Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis Platt, Roy N. Zhang, Yuhua Witherspoon, David J. Xing, Jinchuan Suh, Alexander Keith, Megan S. Jorde, Lynn B. Stevens, Richard D. Ray, David A. Genome Biol Evol Research Article Identification of retrotransposon insertions in nonmodel taxa can be technically challenging and costly. This has inhibited progress in understanding retrotransposon insertion dynamics outside of a few well-studied species. To address this problem, we have extended a retrotransposon-based capture and sequence method (ME-Scan [mobile element scanning]) to identify insertions belonging to the Ves family of short interspersed elements (SINEs) across seven species of the bat genus Myotis. We identified between 120,000 and 143,000 SINE insertions in six taxa lacking a draft genome by comparing to the M. lucifugus reference genome. On average, each Ves insertion was sequenced to 129.6 × coverage. When mapped back to the M. lucifugus reference genome, all insertions were confidently assigned within a 10-bp window. Polymorphic Ves insertions were identified in each taxon based on their mapped locations. Using cross-species comparisons and the identified insertion positions, a presence–absence matrix was created for approximately 796,000 insertions. Dollo parsimony analysis of more than 85,000 phylogenetically informative insertions recovered strongly supported, monophyletic clades that correspond with the biogeography of each taxa. This phylogeny is similar to previously published mitochondrial phylogenies, with the exception of the placement of M. vivesi. These results support the utility of our variation on ME-Scan to identify polymorphic retrotransposon insertions in taxa without a reference genome and for large-scale retrotransposon-based phylogenetics. Oxford University Press 2015-05-25 /pmc/articles/PMC4494050/ /pubmed/26014613 http://dx.doi.org/10.1093/gbe/evv099 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Platt, Roy N.
Zhang, Yuhua
Witherspoon, David J.
Xing, Jinchuan
Suh, Alexander
Keith, Megan S.
Jorde, Lynn B.
Stevens, Richard D.
Ray, David A.
Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis
title Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis
title_full Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis
title_fullStr Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis
title_full_unstemmed Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis
title_short Targeted Capture of Phylogenetically Informative Ves SINE Insertions in Genus Myotis
title_sort targeted capture of phylogenetically informative ves sine insertions in genus myotis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494050/
https://www.ncbi.nlm.nih.gov/pubmed/26014613
http://dx.doi.org/10.1093/gbe/evv099
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