# The methyltransferase activity of Dot1L is essential for Xenopus tropicalis tadpole development and survival

## TL;DR

This study shows that the enzyme Dot1L is essential for the development and survival of Xenopus tropicalis tadpoles by methylating histone H3K79.

## Contribution

The study demonstrates the essential role of Dot1L's methyltransferase activity in Xenopus tropicalis development.

## Key findings

- A Dot1L mutant with no H3K79 methylation leads to tadpole lethality by stage 48.
- Loss of H3K79 methylation causes delayed growth and developmental progression in tadpoles.

## Abstract

Epigenetic modifications of histones play key roles in transcriptional regulation by diverse transcription factors. One such modification is the methylation of histone H3 at lysine 79 (H3K79). The methyltransferase DOT1L is the only known, highly conserved enzyme capable of methylating H3K79 in a wide range of species. We have been studying the role of DOT1L during Xenopus tropicalis development. We have generated a Dot1L mutant line with a deletion of 6 amino acids and two amino acid substitutions in the catalytic domain, resulting in a complete loss of H3K79 methylation in the developing animals. Importantly, we have demonstrated that the absence of H3K79 methylation during X. tropicalis development leads to lethality at or before stage 48 (about 30 days post-fertilization), as well as delayed growth and developmental progression in tadpoles. These findings highlight a crucial role for H3K79 methylation during premetamorphic development of X. tropicalis.

The online version contains supplementary material available at 10.1186/s13578-026-01537-8.