Attenuation of AML1-ETO cellular dysregulation correlates with increased leukemogenic potential
Attenuation of AML1-ETO cellular dysregulation correlates with increased leukemogenic potential
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DOI:
10.1182/blood-2012-11-465641
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发表时间:
2013-05-02
期刊:
影响因子:
20.3
通讯作者:
Zhang, Dong-Er
中科院分区:
文献类型:
--
作者:
DeKelver, Russell C.;Yan, Ming;Zhang, Dong-Er
AML1-ETO (RUNX1-ETO) fusion proteins are generated by the 8; 21 translocation, commonly found in acute myeloid leukemia, which fuses the AML1 (RUNX1) and ETO (MTG8, RUNX1T1) genes. Previous studies have shown that AML1-ETO interferes with AML1 function but requires additional cooperating mutations to induce leukemia development. In mouse models, AML1-ETO forms lacking the C-terminus have been shown to have greatly enhanced leukemogenic potential. Here, we investigate the role of 2 AML1-ETO C-terminal-interacting proteins, N-CoR, a transcriptional corepressor, and SON, a splicing/transcription factor required for cell cycle progression, in AML1-ETO-induced leukemia development. AML1-ETO-W692A loses N-CoR binding at NHR4, displays attenuated transcriptional repression ability and decreased cellular dysregulation, and promotes leukemia in vivo. These results support the importance of the degree of dysregulation by AML1-ETO in cellular transformation and demonstrate that AML1-ETO-W692A can be used as an effective experimental model for determining which factors compromise the leukemogenic potential of AML1-ETO.