Aug 2026· Nature Plants· Vol 12, pp. 1469 - 1484· 0 citations· 120 references
Medicine
TL;DR
This study shows that Arabidopsis thaliana colonizing the Cape Verde Islands rapidly evolved altered DNA methylation patterns through high-impact mutations affecting VIM2/4, CMT2 and FBX5, linked to alternative drought adaptation strategies.
Abstract
DNA methylation is important to maintain genome stability, but alterations in genome-wide methylation patterns can produce widespread genomic effects, with the potential to facilitate rapid adaptation. Here we investigate DNA methylation evolution in Arabidopsis thaliana during its colonization of the drought-prone Cape Verde Islands (CVI). We identified three high-impact changes in genes linking histone modification to DNA methylation that underlie variation in DNA methylation within CVI. We show that gene body methylation is reduced in CVI relative to the Moroccan outgroup due to a 2.7-kb deletion between two VARIANT IN METHYLATIONgenes (VIM2and VIM4), causing aberrant expression of the VIM2/4 homologues. Disruptions of CHROMOMETHYLASE 2 (CMT2) and a newly identified DNA methylation modulator, F-BOX PROTEIN 5 (FBX5), which we validated using CRISPR mutant analysis, contribute to DNA methylation of transposable elements within CVI. Overall, our results reveal rapid methylome evolution driven largely by high-impact variants in three genes. This study shows that Arabidopsis thaliana colonizing the Cape Verde Islands rapidly evolved altered DNA methylation patterns through high-impact mutations affecting VIM2/4, CMT2 and FBX5, linked to alternative drought adaptation strategies.
This study systematically characterizes multi-omics association patterns related to duplicate gene co-expression divergence, providing insights into potential hierarchical regulation and candidate targets for metabolite-directed breeding.
SunTag-NOVA robustly installed DNA methylation and repressed transcription at the endogenous FWA, FT and TMM genes with minimal genome-wide off-target consequences, and establishes SunTag-NOVA as a specific epigenome-editing platform for plants.
Yan He, Ming Wang, T. J. Buckley et al.· bioRxiv· 0 citations
The importance of epigenetics in invasion biology is debated. In particular, the role of epigenetic mechanisms, such as DNA methylation, as potential drivers of rapid adaptation compensating for reduced genetic diversity remains an open question. Introduced to Australia 90 years ago, cane toads (Rhinella marina) are spreading at an ever-increasing rate. Across the invasion range, toads display overall low genetic diversity, yet paradoxically show high phenotypic variation in dispersal-related traits. Here, we use a common-garden experiment to investigate the role of DNA methylation in fostering rapid evolution in this system. We show that toads from newly established populations show distinct DNA methylation profiles to toads from long-colonized areas, particularly in genes putatively involved in dispersal. Epigenetic changes were strongly associated with genetic variation and often overlapped with transposable elements. Our results indicate that epigenetic changes following environmental perturbations have the potential to generate phenotypic variation at ecologically relevant traits in genetically depauperate invasive populations, their molecular interplay with gene activity being complex and probably context-dependent. This article is part of the theme issue 'Ecological epigenetics at the intersection of behaviour and life history variation in non-model animals'.
Boris Yagound, R. R. Sarma, LA Rollins· Philosophical transactions o...· 1 citation
ABSTRACT Transcriptional activation of cell-type-specific genes is achieved by multiple mechanisms that guarantee chromatin accessibility at cis-regulatory elements and the long-range interactions between them. Generally, DNA methylation counteracts these processes and promotes gene silencing in vertebrates. CTCF is a conserved and essential multifunctional transcription factor relevant for establishing and maintaining chromatin architecture and accessibility, while its precise role in regulating DNA methylation remains to be determined. We focused on the highly abundant and previously studied erythroid-specific αD gene (HBAD) to systematically investigate the role of CTCF binding on DNA methylation, chromatin accessibility, and gene expression using a chicken erythroid cell differentiation system. The perturbation of CTCF binding at the intergenic region between the embryonic π and the adult αD gene resulted in DNA methylation propagation towards the αD gene, which was accompanied by decreased chromatin accessibility, GATA-1 binding, and gene expression. Notably, chromatin conformation analyses revealed that CTCF binding enables αD transcriptional activation independently of its architectural function. We observed a similar role of CTCF on DNA methylation and gene expression in the human orthologous gene HBA2. Our findings support a conserved role of CTCF in preventing DNA methylation spreading and gene silencing of cell-type-specific genes along differentiation.
Gustavo Tapia-Urzúa, H. N. Núñez-Martínez, Sylvia Garza-Manero et al.· Epigenetics· 0 citations
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