| Literature DB >> 24497509 |
Jie Xu1, Yue-Ying Wang, Yu-Jun Dai, Wu Zhang, Wei-Na Zhang, Shu-Min Xiong, Zhao-Hui Gu, Kan-Kan Wang, Rong Zeng, Zhu Chen, Sai-Juan Chen.
Abstract
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.Entities:
Keywords: epigenetic abnormality; genomic variation; leukemogenic effect
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Year: 2014 PMID: 24497509 PMCID: PMC3932885 DOI: 10.1073/pnas.1400150111
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205