DNMT3A Arg882 mutation drives chronic myelomonocytic leukemia through disturbing gene expression/DNA methylation in hematopoietic cells

The gene encoding DNA methyltransferase 3A (DNMT3A) is mutated in ∼20% of acute myeloid leukemia cases, with Arg882 (R882) as the hotspot. Here, we addressed the transformation ability of the DNMT3A-Arg882His (R882H) mutant by using a retroviral transduction and bone marrow transplantation (BMT) app...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2014-02, Vol.111 (7), p.2620-2625
Hauptverfasser: Xu, Jie, Wang, Yue-Ying, Dai, Yu-Jun, Zhang, Wu, Zhang, Wei-Na, Xiong, Shu-Min, Gu, Zhao-Hui, Wang, Kan-Kan, Zeng, Rong, Chen, Zhu, Chen, Sai-Juan
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Sprache:eng
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Zusammenfassung:The gene encoding DNA methyltransferase 3A (DNMT3A) is mutated in ∼20% of acute myeloid leukemia cases, with Arg882 (R882) as the hotspot. Here, we addressed the transformation ability of the DNMT3A-Arg882His (R882H) mutant by using a retroviral transduction and bone marrow transplantation (BMT) approach and found that the mutant gene can induce aberrant proliferation of hematopoietic stem/progenitor cells. At 12 mo post-BMT, all mice developed chronic myelomonocytic leukemia with thrombocytosis. RNA microarray analysis revealed abnormal expressions of some hematopoiesis-related genes, and the DNA methylation assay identified corresponding changes in methylation patterns in gene body regions. Moreover, DNMT3A-R882H increased the CDK1 protein level and enhanced cell-cycle activity, thereby contributing to leukemogenesis.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1400150111