A molecular switch between mammalian MLL complexes dictates response to Menin-MLL inhibition

Soto-Feliciano, Y. M.; Sanchez-Rivera, F. J.; Perner, F.; Barrows, D. W.; Kastenhuber, E. R.; Ho, Y.-J.; Carroll, T.; Xiong, Y.; Soshnev, A.; Gates, L.; Beytagh, M. C.; Cheon, D.; Gu, S.; Liu, X. S.; Krivtsov, A. V.; Meneses, M.; de Stanchina, E.; Stone, R. M.; Armstrong, S. A.; Lowe, S. W.; Allis, C. D.

doi:10.1101/2021.10.22.465184

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bioRxiv · 10.1101/2021.10.22.465184

A molecular switch between mammalian MLL complexes dictates response to Menin-MLL inhibition

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Abstract

The chromatin adaptor Menin interacts with oncogenic fusion proteins encoded by MLL1-rearrangements (MLL1-r), and small molecules that disrupt these associations are currently in clinical trials for the treatment of leukemia. By integrating chromatin-focused and genome-wide CRISPR screens with genetic, pharmacological, and biochemical approaches in mouse and human systems, we discovered a molecular switch between the MLL1-Menin and MLL3/4-UTX chromatin modifying complexes that dictates response to Menin-MLL inhibitors. We show that MLL1-Menin safeguards leukemia survival by impeding binding of the MLL3/4-UTX complex at a subset of target gene promoters. Disrupting the interaction between Menin and MLL1 leads to UTX-dependent transcriptional activation of a tumor suppressor gene-program that is crucial for a therapeutic response in murine and human leukemia. We establish the therapeutic relevance of this mechanism by showing that CDK4/6 inhibitors allow re-activation of this tumor-suppressor program in Menin-inhibitor insensitive leukemia cells, mitigating treatment resistance. The discovery of a molecular switch between MLL1-Menin and MLL3/4-UTX complexes on chromatin sheds light on novel functions of these evolutionary conserved epigenetic mediators and is particularly relevant to understand and target molecular pathways determining response and resistance in ongoing phase 1/2 clinical trials.

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Soto-Feliciano, Y. M., Sanchez-Rivera, F. J., Perner, F., Barrows, D. W., Kastenhuber, E. R., Ho, Y.-J., Carroll, T., Xiong, Y., Soshnev, A., Gates, L., Beytagh, M. C., Cheon, D., Gu, S., Liu, X. S., Krivtsov, A. V., Meneses, M., de Stanchina, E., Stone, R. M., Armstrong, S. A., Lowe, S. W., Allis, C. D.. 2021-10-22. A molecular switch between mammalian MLL complexes dictates response to Menin-MLL inhibition. https://doi.org/10.1101/2021.10.22.465184

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