Active DNA demethylation of developmental cis-regulatory regions predates vertebrate origins
Ksenia SkvortsovaiD, Stéphanie BertrandiD, Danila VoronoviD, Paul E. Duckett, Samuel E. RossiD, Marta Silvia MagriiD, Ignacio MaesoiD, Robert J. WeatherittiD, José Luis Gómez-SkármetaiD, Maria Ina ArnoneiD, Héctor EscriváiD, Ozren BogdanovićiD
Abstract
DNA methylation (5-methylcytosine; 5mC) is a repressive gene-regulatory mark required for vertebrate embryogenesis. Genomic 5mC is tightly regulated through the coordinated action of DNA methyltransferases, which deposit 5mC, and TET enzymes, which participate in its active removal through the formation of 5-hydroxymethylcytosine (5hmC). TET enzymes are essential for mammalian gastrulation and activation of vertebrate developmental enhancers, however, to date, a clear picture of 5hmC function, abundance, and genomic distribution in non-vertebrate lineages is lacking. By employing base-resolution 5mC and 5hmC quantification during sea urchin and lancelet embryogenesis, we shed light on the roles of non-vertebrate 5hmC and TET enzymes. We find that these invertebrate deuterostomes employ TET enzymes for targeted demethylation of regulatory regions associated with developmental genes and show that the complement of identified 5hmC-regulated genes is conserved to vertebrates. This work thus demonstrates that active 5mC removal from regulatory regions is a common feature of deuterostome embryogenesis suggestive of unexpected deep conservation of a major gene-regulatory module.
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