Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elements

Ultraconserved noncoding elements (UCNEs) constitute less than 1 Mb of vertebrate genomes and are impervious to accumulating mutations. About 4000 UCNEs exist in vertebrate genomes, each at least 200 nucleotides in length, sharing greater than 95% sequence identity between human and chicken. Despite...

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Main Authors: Mathia Colwell, Melissa Drown, Kelly Showel, Chelsea Drown, Amanda Palowski, Christopher Faulk
Format: Article
Language:English
Published: Taylor & Francis Group 2018-01-01
Series:Epigenetics
Subjects:
Online Access:http://dx.doi.org/10.1080/15592294.2017.1411447
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author Mathia Colwell
Melissa Drown
Kelly Showel
Chelsea Drown
Amanda Palowski
Christopher Faulk
author_facet Mathia Colwell
Melissa Drown
Kelly Showel
Chelsea Drown
Amanda Palowski
Christopher Faulk
author_sort Mathia Colwell
collection DOAJ
description Ultraconserved noncoding elements (UCNEs) constitute less than 1 Mb of vertebrate genomes and are impervious to accumulating mutations. About 4000 UCNEs exist in vertebrate genomes, each at least 200 nucleotides in length, sharing greater than 95% sequence identity between human and chicken. Despite extreme sequence conservation over 400 million years of vertebrate evolution, we show both ordered interspecies and within-species interindividual variation in DNA methylation in these regions. Here, we surveyed UCNEs with high CpG density in 56 species finding half to be intermediately methylated and the remaining near 0% or 100%. Intermediately methylated UCNEs displayed a greater range of methylation between mouse tissues. In a human population, most UCNEs showed greater variation than the LINE1 transposon, a frequently used epigenetic biomarker. Global methylation was found to be inversely correlated to hydroxymethylation across 60 vertebrates. Within UCNEs, DNA methylation is flexible, conserved between related species, and relaxed from the underlying sequence selection pressure, while remaining heritable through speciation.
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spelling doaj.art-174e78d6757b47b49640c9540f5e918a2023-09-21T13:09:20ZengTaylor & Francis GroupEpigenetics1559-22941559-23082018-01-01131496010.1080/15592294.2017.14114471411447Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elementsMathia Colwell0Melissa Drown1Kelly Showel2Chelsea Drown3Amanda Palowski4Christopher Faulk5University of Minnesota, College of Food, Agricultural, and Natural Resource SciencesUniversity of Minnesota, College of Food, Agricultural, and Natural Resource SciencesUniversity of Minnesota, College of Food, Agricultural, and Natural Resource SciencesUniversity of Minnesota, College of Food, Agricultural, and Natural Resource SciencesUniversity of Minnesota, College of Food, Agricultural, and Natural Resource SciencesUniversity of Minnesota, College of Food, Agricultural, and Natural Resource SciencesUltraconserved noncoding elements (UCNEs) constitute less than 1 Mb of vertebrate genomes and are impervious to accumulating mutations. About 4000 UCNEs exist in vertebrate genomes, each at least 200 nucleotides in length, sharing greater than 95% sequence identity between human and chicken. Despite extreme sequence conservation over 400 million years of vertebrate evolution, we show both ordered interspecies and within-species interindividual variation in DNA methylation in these regions. Here, we surveyed UCNEs with high CpG density in 56 species finding half to be intermediately methylated and the remaining near 0% or 100%. Intermediately methylated UCNEs displayed a greater range of methylation between mouse tissues. In a human population, most UCNEs showed greater variation than the LINE1 transposon, a frequently used epigenetic biomarker. Global methylation was found to be inversely correlated to hydroxymethylation across 60 vertebrates. Within UCNEs, DNA methylation is flexible, conserved between related species, and relaxed from the underlying sequence selection pressure, while remaining heritable through speciation.http://dx.doi.org/10.1080/15592294.2017.1411447epigeneticsdna methylationphylogenetic least squarescpg densityevolutionvarmintsultraconserved noncoding elements
spellingShingle Mathia Colwell
Melissa Drown
Kelly Showel
Chelsea Drown
Amanda Palowski
Christopher Faulk
Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elements
Epigenetics
epigenetics
dna methylation
phylogenetic least squares
cpg density
evolution
varmints
ultraconserved noncoding elements
title Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elements
title_full Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elements
title_fullStr Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elements
title_full_unstemmed Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elements
title_short Evolutionary conservation of DNA methylation in CpG sites within ultraconserved noncoding elements
title_sort evolutionary conservation of dna methylation in cpg sites within ultraconserved noncoding elements
topic epigenetics
dna methylation
phylogenetic least squares
cpg density
evolution
varmints
ultraconserved noncoding elements
url http://dx.doi.org/10.1080/15592294.2017.1411447
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