JMJD1C forms condensate to facilitate a RUNX1-dependent gene expression program shared by multiple types of AML cells

JMJD1C (Jumonji Domain Containing 1C), a member of the lysine demethylase 3 (KDM3) family, is universally required for the survival of several types of acute myeloid leukemia (AML) cells with different genetic mutations, representing a therapeutic opportunity with broad application. Yet how JMJD1C regulates the leukemic programs of various AML cells is largely unexplored. Here we show that JMJD1C interacts with the master hematopoietic transcription factor RUNX1, which thereby recruits JMJD1C to the genome to facilitate a RUNX1-driven transcriptional program that supports leukemic cell survival. The underlying mechanism hinges on the long N-terminal disordered region of JMJD1C, which harbors two inseparable abilities: condensate formation and direct interaction with RUNX1. This dual capability of JMJD1C may influence enhancer-promoter contacts crucial for the expression of key leukemic genes regulated by RUNX1. Our findings demonstrate a previously unappreciated role for the non-catalytic function of JMJD1C in transcriptional regulation, underlying a mechanism shared by different types of leukemias.

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Publication Details

Journal
Protein & Cell
Published
2024-10-25
DOI
https://doi.org/10.1093/procel/pwae059
Citations
4
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
1.82

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article

JMJD1C forms condensate to facilitate a RUNX1-dependent gene expression program shared by multiple types of AML cells

Pilong Li, Christopher R. Vakoc, Saisai Wang, Zhuoran Zhen et al.
4 citations
Protein & Cell
Acute Myeloid Leukemia Research
1.82
article

JMJD1C forms condensate to facilitate a RUNX1-dependent gene expression program shared by multiple types of AML cells

Pilong Li, Christopher R. Vakoc, Saisai Wang, Zhuoran Zhen, Juqing Zhang, Jiajun Zhu, Jie He, Rong Li, Haifeng Wang, Mo Chen, Qian Chen, Bin Lü, Min Xie, R G Roeder, Jing Li
article en
4 citations

Abstract

JMJD1C (Jumonji Domain Containing 1C), a member of the lysine demethylase 3 (KDM3) family, is universally required for the survival of several types of acute myeloid leukemia (AML) cells with different genetic mutations, representing a therapeutic opportunity with broad application. Yet how JMJD1C regulates the leukemic programs of various AML cells is largely unexplored. Here we show that JMJD1C interacts with the master hematopoietic transcription factor RUNX1, which thereby recruits JMJD1C to the genome to facilitate a RUNX1-driven transcriptional program that supports leukemic cell survival. The underlying mechanism hinges on the long N-terminal disordered region of JMJD1C, which harbors two inseparable abilities: condensate formation and direct interaction with RUNX1. This dual capability of JMJD1C may influence enhancer-promoter contacts crucial for the expression of key leukemic genes regulated by RUNX1. Our findings demonstrate a previously unappreciated role for the non-catalytic function of JMJD1C in transcriptional regulation, underlying a mechanism shared by different types of leukemias.

Protein & CellVol. 16(5)
Shanxi Medical University (CN), Second Military Medical University (CN), Peking University (CN), Cold Spring Harbor Laboratory (US), King Center (US), Changhai Hospital (CN), Center for Life Sciences (CN), Rockefeller University (US), Tsinghua University (CN)
Leukemia and Lymphoma Society, National Natural Science Foundation of China, Tsinghua University
Good health and well-being
Openalex Percentile: Top 14%
Acute Myeloid Leukemia Research
1.82
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