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Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals

Broad paradigms of vertebrate genomic repeat element evolution have been largely shaped by analyses of mammalian and avian genomes. Here, based on analyses of genomes sequenced from over 60 squamate reptiles (lizards and snakes), we show that patterns of genomic repeat landscape evolution in squamat...

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Autores principales: Pasquesi, Giulia I. M., Adams, Richard H., Card, Daren C., Schield, Drew R., Corbin, Andrew B., Perry, Blair W., Reyes-Velasco, Jacobo, Ruggiero, Robert P., Vandewege, Michael W., Shortt, Jonathan A., Castoe, Todd A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050309/
https://www.ncbi.nlm.nih.gov/pubmed/30018307
http://dx.doi.org/10.1038/s41467-018-05279-1
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author Pasquesi, Giulia I. M.
Adams, Richard H.
Card, Daren C.
Schield, Drew R.
Corbin, Andrew B.
Perry, Blair W.
Reyes-Velasco, Jacobo
Ruggiero, Robert P.
Vandewege, Michael W.
Shortt, Jonathan A.
Castoe, Todd A.
author_facet Pasquesi, Giulia I. M.
Adams, Richard H.
Card, Daren C.
Schield, Drew R.
Corbin, Andrew B.
Perry, Blair W.
Reyes-Velasco, Jacobo
Ruggiero, Robert P.
Vandewege, Michael W.
Shortt, Jonathan A.
Castoe, Todd A.
author_sort Pasquesi, Giulia I. M.
collection PubMed
description Broad paradigms of vertebrate genomic repeat element evolution have been largely shaped by analyses of mammalian and avian genomes. Here, based on analyses of genomes sequenced from over 60 squamate reptiles (lizards and snakes), we show that patterns of genomic repeat landscape evolution in squamates challenge such paradigms. Despite low variance in genome size, squamate genomes exhibit surprisingly high variation among species in abundance (ca. 25–73% of the genome) and composition of identifiable repeat elements. We also demonstrate that snake genomes have experienced microsatellite seeding by transposable elements at a scale unparalleled among eukaryotes, leading to some snake genomes containing the highest microsatellite content of any known eukaryote. Our analyses of transposable element evolution across squamates also suggest that lineage-specific variation in mechanisms of transposable element activity and silencing, rather than variation in species-specific demography, may play a dominant role in driving variation in repeat element landscapes across squamate phylogeny.
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spelling pubmed-60503092018-07-23 Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals Pasquesi, Giulia I. M. Adams, Richard H. Card, Daren C. Schield, Drew R. Corbin, Andrew B. Perry, Blair W. Reyes-Velasco, Jacobo Ruggiero, Robert P. Vandewege, Michael W. Shortt, Jonathan A. Castoe, Todd A. Nat Commun Article Broad paradigms of vertebrate genomic repeat element evolution have been largely shaped by analyses of mammalian and avian genomes. Here, based on analyses of genomes sequenced from over 60 squamate reptiles (lizards and snakes), we show that patterns of genomic repeat landscape evolution in squamates challenge such paradigms. Despite low variance in genome size, squamate genomes exhibit surprisingly high variation among species in abundance (ca. 25–73% of the genome) and composition of identifiable repeat elements. We also demonstrate that snake genomes have experienced microsatellite seeding by transposable elements at a scale unparalleled among eukaryotes, leading to some snake genomes containing the highest microsatellite content of any known eukaryote. Our analyses of transposable element evolution across squamates also suggest that lineage-specific variation in mechanisms of transposable element activity and silencing, rather than variation in species-specific demography, may play a dominant role in driving variation in repeat element landscapes across squamate phylogeny. Nature Publishing Group UK 2018-07-17 /pmc/articles/PMC6050309/ /pubmed/30018307 http://dx.doi.org/10.1038/s41467-018-05279-1 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pasquesi, Giulia I. M.
Adams, Richard H.
Card, Daren C.
Schield, Drew R.
Corbin, Andrew B.
Perry, Blair W.
Reyes-Velasco, Jacobo
Ruggiero, Robert P.
Vandewege, Michael W.
Shortt, Jonathan A.
Castoe, Todd A.
Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals
title Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals
title_full Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals
title_fullStr Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals
title_full_unstemmed Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals
title_short Squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals
title_sort squamate reptiles challenge paradigms of genomic repeat element evolution set by birds and mammals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050309/
https://www.ncbi.nlm.nih.gov/pubmed/30018307
http://dx.doi.org/10.1038/s41467-018-05279-1
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