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

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.

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Journal
Cell & Bioscience
Published
2026-03-03
DOI
https://doi.org/10.1186/s13578-026-01537-8
Primary Topic
Epigenetics and DNA Methylation
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Laurent M. Sachs, Yun‐Bo Shi, Nga Luu, Emeric Louis
Cell & Bioscience
Epigenetics and DNA Methylation
article

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

Laurent M. Sachs, Yun‐Bo Shi, Nga Luu, Emeric Louis
article en

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.

Cell & BioscienceVol. 16(1)
Centre National de la Recherche Scientifique (FR), National Institutes of Health (US), Sorbonne Université (FR), Eunice Kennedy Shriver National Institute of Child Health and Human Development (US), Molécules de Communication et Adaptation des Micro-organismes (FR)
U.S. Department of Health and Human Services, National Institutes of Health
Openalex Percentile: Top 35%
Epigenetics and DNA Methylation
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