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Slow DNA Loss in the Gigantic Genomes of Salamanders

Evolutionary changes in genome size result from the combined effects of mutation, natural selection, and genetic drift. Insertion and deletion mutations (indels) directly impact genome size by adding or removing sequences. Most species lose more DNA through small indels (i.e., ∼1–30 bp) than they ga...

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Autores principales: Sun, Cheng, López Arriaza, José R., Mueller, Rachel Lockridge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542557/
https://www.ncbi.nlm.nih.gov/pubmed/23175715
http://dx.doi.org/10.1093/gbe/evs103
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author Sun, Cheng
López Arriaza, José R.
Mueller, Rachel Lockridge
author_facet Sun, Cheng
López Arriaza, José R.
Mueller, Rachel Lockridge
author_sort Sun, Cheng
collection PubMed
description Evolutionary changes in genome size result from the combined effects of mutation, natural selection, and genetic drift. Insertion and deletion mutations (indels) directly impact genome size by adding or removing sequences. Most species lose more DNA through small indels (i.e., ∼1–30 bp) than they gain, which can result in genome reduction over time. Because this rate of DNA loss varies across species, small indel dynamics have been suggested to contribute to genome size evolution. Species with extremely large genomes provide interesting test cases for exploring the link between small indels and genome size; however, most large genomes remain relatively unexplored. Here, we examine rates of DNA loss in the tetrapods with the largest genomes—the salamanders. We used low-coverage genomic shotgun sequence data from four salamander species to examine patterns of insertion, deletion, and substitution in neutrally evolving non-long terminal repeat (LTR) retrotransposon sequences. For comparison, we estimated genome-wide DNA loss rates in non-LTR retrotransposon sequences from five other vertebrate genomes: Anolis carolinensis, Danio rerio, Gallus gallus, Homo sapiens, and Xenopus tropicalis. Our results show that salamanders have significantly lower rates of DNA loss than do other vertebrates. More specifically, salamanders experience lower numbers of deletions relative to insertions, and both deletions and insertions are skewed toward smaller sizes. On the basis of these patterns, we conclude that slow DNA loss contributes to genomic gigantism in salamanders. We also identify candidate molecular mechanisms underlying these differences and suggest that natural variation in indel dynamics provides a unique opportunity to study the basis of genome stability.
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spelling pubmed-35425572013-01-11 Slow DNA Loss in the Gigantic Genomes of Salamanders Sun, Cheng López Arriaza, José R. Mueller, Rachel Lockridge Genome Biol Evol Research Article Evolutionary changes in genome size result from the combined effects of mutation, natural selection, and genetic drift. Insertion and deletion mutations (indels) directly impact genome size by adding or removing sequences. Most species lose more DNA through small indels (i.e., ∼1–30 bp) than they gain, which can result in genome reduction over time. Because this rate of DNA loss varies across species, small indel dynamics have been suggested to contribute to genome size evolution. Species with extremely large genomes provide interesting test cases for exploring the link between small indels and genome size; however, most large genomes remain relatively unexplored. Here, we examine rates of DNA loss in the tetrapods with the largest genomes—the salamanders. We used low-coverage genomic shotgun sequence data from four salamander species to examine patterns of insertion, deletion, and substitution in neutrally evolving non-long terminal repeat (LTR) retrotransposon sequences. For comparison, we estimated genome-wide DNA loss rates in non-LTR retrotransposon sequences from five other vertebrate genomes: Anolis carolinensis, Danio rerio, Gallus gallus, Homo sapiens, and Xenopus tropicalis. Our results show that salamanders have significantly lower rates of DNA loss than do other vertebrates. More specifically, salamanders experience lower numbers of deletions relative to insertions, and both deletions and insertions are skewed toward smaller sizes. On the basis of these patterns, we conclude that slow DNA loss contributes to genomic gigantism in salamanders. We also identify candidate molecular mechanisms underlying these differences and suggest that natural variation in indel dynamics provides a unique opportunity to study the basis of genome stability. Oxford University Press 2012 2012-11-22 /pmc/articles/PMC3542557/ /pubmed/23175715 http://dx.doi.org/10.1093/gbe/evs103 Text en © The Author(s) 2012. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sun, Cheng
López Arriaza, José R.
Mueller, Rachel Lockridge
Slow DNA Loss in the Gigantic Genomes of Salamanders
title Slow DNA Loss in the Gigantic Genomes of Salamanders
title_full Slow DNA Loss in the Gigantic Genomes of Salamanders
title_fullStr Slow DNA Loss in the Gigantic Genomes of Salamanders
title_full_unstemmed Slow DNA Loss in the Gigantic Genomes of Salamanders
title_short Slow DNA Loss in the Gigantic Genomes of Salamanders
title_sort slow dna loss in the gigantic genomes of salamanders
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3542557/
https://www.ncbi.nlm.nih.gov/pubmed/23175715
http://dx.doi.org/10.1093/gbe/evs103
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