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Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
RNA m6A reader YTHDF2 facilitates precursor miR-126 maturation to promote acute myeloid leukemia progression
Zheng Zhang1,2, Keren Zhou1, Li Han1,3
1Department of Systems Biology, Beckman Research Institute of City of Hope, Monrovia, CA 91016, USA.
Abstract:
As the most common internal modification of mRNA, N6-methyladenosine (m6A) and its regulators modulate gene expression and play critical roles in various biological and pathological processes including tumorigenesis. It was reported previously that m6A methyltransferase (writer), methyltransferase-like 3 (METTL3) adds m6A in primary microRNAs (pri-miRNAs) and facilitates its processing into precursor miRNAs (pre-miRNAs). However, it is unknown whether m6A modification also plays a role in the maturation process of pre-miRNAs and (if so) whether such a function contributes to tumorigenesis. Here, we found that YTHDF2 is aberrantly overexpressed in acute myeloid leukemia (AML) patients, especially in relapsed patients, and plays an oncogenic role in AML. Moreover, YTHDF2 promotes expression of miR-126-3p (also known as miR-126, as it is the main product of precursor miR-126 (pre-miR-126)), a miRNA that was reported as an oncomiRNA in AML, through facilitating the processing of pre-miR-126 into mature miR-126. Mechanistically, YTHDF2 recognizes m6A modification in pre-miR-126 and recruits AGO2, a regulator of pre-miRNA processing, to promote the maturation of pre-miR-126. YTHDF2 positively and negatively correlates with miR-126 and miR-126's downstream target genes, respectively, in AML patients, and forced expression of miR-126 could largely rescue YTHDF2/Ythdf2 depletion-mediated suppression on AML cell growth/proliferation and leukemogenesis, indicating that miR-126 is a functionally important target of YTHDF2 in AML. Overall, our studies not only reveal a previously unappreciated YTHDF2/miR-126 axis in AML and highlight the therapeutic potential of targeting this axis for AML treatment, but also suggest that m6A plays a role in pre-miRNA processing that contributes to tumorigenesis.
Insights
YTHDF2 promotes acute myeloid leukemia (AML) by enhancing miR-126 maturation via N-methyladenosine (m6A) modification. Targeting this YTHDF2/miR-126 pathway offers potential therapeutic strategies for AML treatment.
Area of Science:
- Epigenetics and RNA modifications
- Molecular oncology
- Gene expression regulation
Background:
- N-methyladenosine (m6A) is a common mRNA modification influencing gene expression and tumorigenesis.
- METTL3, an m6A writer, processes pri-miRNAs into pre-miRNAs.
- The role of m6A in pre-miRNA maturation and its contribution to cancer remain largely unexplored.
Purpose of the Study:
- To investigate the role of m6A modification in pre-miRNA processing.
- To determine the function of YTH domain-containing protein 2 (YTHDF2) in acute myeloid leukemia (AML).
- To elucidate the YTHDF2/miR-126 axis in AML pathogenesis and therapeutic potential.
Main Methods:
- Analysis of YTHDF2 expression in AML patients, including relapsed cases.
- Investigating YTHDF2's role in pre-miR-126 processing and miR-126 maturation.
- Mechanistic studies involving m6A recognition, AGO2 recruitment, and correlation analysis in AML patient data.
Main Results:
- YTHDF2 is overexpressed in AML patients and promotes leukemogenesis.
- YTHDF2 facilitates pre-miR-126 processing into mature miR-126, an oncomiRNA in AML.
- YTHDF2 binds to m6A-modified pre-miR-126, recruiting AGO2 to promote maturation; miR-126 is a key downstream target of YTHDF2 in AML.
Conclusions:
- The study reveals a novel YTHDF2/miR-126 axis critical for AML progression.
- m6A modification plays a role in pre-miRNA processing, contributing to tumorigenesis.
- Targeting the YTHDF2/miR-126 pathway presents a promising therapeutic strategy for AML.
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