The tumor suppressor MIR139 is silenced by POLR2M to promote AML oncogenesis
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
34741119
PubMed Central
PMC8885418
DOI
10.1038/s41375-021-01461-5
PII: 10.1038/s41375-021-01461-5
Knihovny.cz E-resources
- MeSH
- Leukemia, Myeloid, Acute genetics MeSH
- Epigenesis, Genetic MeSH
- Oncogene Proteins, Fusion genetics MeSH
- Carcinogenesis genetics MeSH
- Humans MeSH
- MicroRNAs genetics MeSH
- Mice, Inbred C57BL MeSH
- Mice, Knockout MeSH
- Mice MeSH
- Cell Line, Tumor MeSH
- Myeloid-Lymphoid Leukemia Protein genetics MeSH
- Gene Expression Regulation, Leukemic MeSH
- RNA Polymerase II genetics MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Oncogene Proteins, Fusion MeSH
- MicroRNAs MeSH
- MIRN139 microRNA, human MeSH Browser
- MIRN139 microRNA, mouse MeSH Browser
- MLL-AF9 fusion protein, human MeSH Browser
- POLR2M protein, human MeSH Browser
- Polr2m protein, mouse MeSH Browser
- Myeloid-Lymphoid Leukemia Protein MeSH
- RNA Polymerase II MeSH
MIR139 is a tumor suppressor and is commonly silenced in acute myeloid leukemia (AML). However, the tumor-suppressing activities of miR-139 and molecular mechanisms of MIR139-silencing remain largely unknown. Here, we studied the poorly prognostic MLL-AF9 fusion protein-expressing AML. We show that MLL-AF9 expression in hematopoietic precursors caused epigenetic silencing of MIR139, whereas overexpression of MIR139 inhibited in vitro and in vivo AML outgrowth. We identified novel miR-139 targets that mediate the tumor-suppressing activities of miR-139 in MLL-AF9 AML. We revealed that two enhancer regions control MIR139 expression and found that the polycomb repressive complex 2 (PRC2) downstream of MLL-AF9 epigenetically silenced MIR139 in AML. Finally, a genome-wide CRISPR-Cas9 knockout screen revealed RNA Polymerase 2 Subunit M (POLR2M) as a novel MIR139-regulatory factor. Our findings elucidate the molecular control of tumor suppressor MIR139 and reveal a role for POLR2M in the MIR139-silencing mechanism, downstream of MLL-AF9 and PRC2 in AML. In addition, we confirmed these findings in human AML cell lines with different oncogenic aberrations, suggesting that this is a more common oncogenic mechanism in AML. Our results may pave the way for new targeted therapy in AML.
Center for Proteomics and Metabolomics Leiden University Medical Center Leiden the Netherlands
Erasmus MC University Medical Center Rotterdam Center for Biomics Rotterdam the Netherlands
Erasmus MC University Medical Center Rotterdam Department of Cell Biology Rotterdam the Netherlands
Erasmus MC University Medical Center Rotterdam Department of Hematology Rotterdam the Netherlands
Erasmus MC University Medical Center Rotterdam Department of Immunology Rotterdam the Netherlands
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