DNA methylation deposition is dependent on the presence of H3K4me3 and H3K36me3 histone marks.

Phosphate starvation in rice induces widespread, but transient, modulation of DNA methylation near stress responsive genes that is independent from the RNA-directed DNA methylation pathway.

The various transposon families of the mammalian genome can adopt different types of repressive chromatin responses upon DNA methylation loss.

The adaptation of Arabidopsis plants to the local environment is linked to DNA methylation.

mSTARR-seq identifies regions of the genome where DNA methylation causally impacts gene expression, providing a map of which epigenetic marks may influence trait variation.

Nucleosomes and linker histones block eukaryotic cytosine methylation.

Active DNA demethylation at some defence gene promoters is causal for DNA binding of WRKY transcription factors as well as for transcriptional activation of these genes during plant immune response.

Transposon activation during male gametogenesis is caused by interactions between DNA demethylation and linker histone H1, developmental depletion of which promotes pollen fertility.

Simultaneous targeting of loci by pathways that promote euchromatin and heterochromatin primes transcribed genes for epimutations in the form of CG DNA methylation.

Epigenetic modifications to DNA can regulate E3 ubiquitin ligase activity in human cells.