RRC ID 90103
Author Neville D, Ferguson DT, Heikamp EB, Lai Z, Magor GW, Lam C, Dobbs OG, Levina V, Knezevic K, The JJ, Alex S, Suits SC, Rumler B, Uckelmann M, Talarmain L, Lam EYN, Perkins AC, Armstrong SA, Bell CC, Davidovich C, Gilan O.
Title DOT1L provides transcriptional memory through PRC1.1 antagonism.
Journal Nat Cell Biol
Abstract DOT1L and Menin are essential cofactors for the oncogenic activity of MLL fusion proteins (MLL-FPs) in leukaemia. However, the mechanisms underpinning the therapeutic effects of their inhibitors remain unclear. Here we identify a critical role for the non-canonical Polycomb repressive complex 1.1 (PRC1.1) in mediating the cellular responses to DOT1L and Menin inhibitors. Menin inhibition induces PRC1.1-dependent deposition of H2AK119ub to silence a subset of MLL-FP targets, whereas DOT1L inhibition results in a genome-wide increase in H2AK119ub. We show that enhanced PRC1.1 activity arises specifically from the progressive loss of DOT1L-mediated H3K79 methylation, independent of MLL-FP displacement or transcriptional repression. This regulatory crosstalk is conserved across cell types and is driven by direct biochemical antagonism between H3K79 methylation and PRC1 activity. Together, our findings establish DOT1L as a component of transcriptional memory co-opted in leukaemia and suggest it serves as the missing link balancing the opposing forces of the MLL-Polycomb axis.
Volume 28(2)
Pages 307-322
Published 2026-2-1
DOI 10.1038/s41556-025-01859-8
PII 10.1038/s41556-025-01859-8
PMID 41634341
PMC PMC12904788
MeSH Animals Cell Line, Tumor Histone-Lysine N-Methyltransferase* / genetics Histone-Lysine N-Methyltransferase* / metabolism Histones / genetics Histones / metabolism Humans Leukemia* / enzymology Leukemia* / genetics Leukemia* / pathology Methylation Methyltransferases* / genetics Methyltransferases* / metabolism Myeloid-Lymphoid Leukemia Protein / genetics Myeloid-Lymphoid Leukemia Protein / metabolism Oncogene Proteins, Fusion / genetics Oncogene Proteins, Fusion / metabolism Polycomb Repressive Complex 1* / antagonists & inhibitors Polycomb Repressive Complex 1* / genetics Polycomb Repressive Complex 1* / metabolism Proto-Oncogene Proteins* / antagonists & inhibitors Proto-Oncogene Proteins* / genetics Proto-Oncogene Proteins* / metabolism Transcription, Genetic* / drug effects
Resource
Human and Animal Cells HUDEP-2(RCB4557)