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Denkena, J. ; Johannes, F.* ; Colomé-Tatché, M.

Region-level epimutation rates in Arabidopsis thaliana.

Heredity 127, 190–202 (2021)
Publ. Version/Full Text DOI PMC
Open Access Hybrid
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Failure to maintain DNA methylation patterns during plant development can occasionally give rise to so-called “spontaneous epimutations”. These stochastic methylation changes are sometimes heritable across generations and thus accumulate in plant genomes over time. Recent evidence indicates that spontaneous epimutations have a major role in shaping patterns of methylation diversity in plant populations. Using single CG dinucleotides as units of analysis, previous work has shown that the epimutation rate is several orders of magnitude higher than the genetic mutation rate. While these large rate differences have obvious implications for understanding genome-methylome co-evolution, the functional relevance of single CG methylation changes remains questionable. In contrast to single CG, solid experimental evidence has linked methylation gains and losses in larger genomic regions with transcriptional variation and heritable phenotypic effects. Here we show that such region-level changes arise stochastically at about the same rate as those at individual CG sites, are only marginal dependent on region size and cytosine density, but strongly dependent on chromosomal location. We also find consistent evidence that region-level epimutations are not restricted to CG contexts but also frequently occur in non-CG regions at the genome-wide scale. Taken together, our results support the view that many differentially methylated regions (DMRs) in natural populations originate from epimutation events and may not be effectively tagged by proximal SNPs. This possibility reinforces the need for epigenome-wide association studies (EWAS) in plants as a way to identify the epigenetic basis of complex traits.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Dna Methylation; Consequences; Methylome; Dynamics; Patterns
Language english
Publication Year 2021
HGF-reported in Year 2021
ISSN (print) / ISBN 0018-067X
e-ISSN 1365-2540
Journal Heredity
Quellenangaben Volume: 127, Issue: , Pages: 190–202 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Publishing Place Campus, 4 Crinan St, London, N1 9xw, England
Reviewing status Peer reviewed
POF-Topic(s) 30205 - Bioengineering and Digital Health
Research field(s) Enabling and Novel Technologies
PSP Element(s) G-554200-001
Grants
Helmholtz Association
Scopus ID 85105445451
PubMed ID 33966050
Erfassungsdatum 2021-06-21