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 .
Louis et al. (Tue,) studied this question.