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AML1/ETO与CBFβ的异源二聚化是白血病发生所必需的,但对于骨髓增殖并非必需。

Heterodimerization of AML1/ETO with CBFβ is required for leukemogenesis but not for myeloproliferation.

作者信息

Thiel V N, Giaimo B D, Schwarz P, Soller K, Vas V, Bartkuhn M, Blätte T J, Döhner K, Bullinger L, Borggrefe T, Geiger H, Oswald F

机构信息

University Medical Center Ulm, Center for Internal Medicine, Department of Internal Medicine I, University of Ulm, Ulm, Germany.

Institute of Biochemistry, University of Giessen, Giessen, Germany.

出版信息

Leukemia. 2017 Nov;31(11):2491-2502. doi: 10.1038/leu.2017.105. Epub 2017 Mar 31.

Abstract

The AML1/Runx1 transcription factor and its heterodimerization partner CBFβ are essential regulators of myeloid differentiation. The chromosomal translocation t(8;21), fusing the DNA binding domain of AML1 to the corepressor eight-twenty-one (ETO), is frequently associated with acute myeloid leukemia and generates the AML1/ETO (AE) fusion protein. AE represses target genes usually activated by AML1 and also affects the endogenous repressive function of ETO at Notch target genes. In order to analyze the contribution of CBFβ in AE-mediated leukemogenesis and deregulation of Notch target genes, we introduced two point mutations in a leukemia-initiating version of AE in mice, called AE9a, that disrupt the AML1/CBFβ interaction (AE9aNT). We report that the AE9a/CBFβ interaction is not required for the AE9a-mediated aberrant expression of AML1 target genes, while upregulation/derepression of Notch target genes does require the interaction with CBFβ. Using retroviral transduction to express AE9a in murine adult bone marrow-derived hematopoietic progenitors, we observed that both AE9a and AE9aNT lead to increased myeloproliferation in vivo. However, both development of leukemia and long-term replating capacity are only observed with AE9a but not with AE9aNT. Thus, deregulation of both AML1 and Notch target genes is required for the development of AE9a-driven leukemia.

摘要

AML1/Runx1转录因子及其异二聚体伴侣CBFβ是髓系分化的关键调节因子。染色体易位t(8;21)将AML1的DNA结合结构域与共抑制因子八二十一(ETO)融合,这常与急性髓系白血病相关,并产生AML1/ETO(AE)融合蛋白。AE抑制通常由AML1激活的靶基因,还影响ETO在Notch靶基因处的内源性抑制功能。为了分析CBFβ在AE介导的白血病发生和Notch靶基因失调中的作用,我们在小鼠中一种白血病起始型的AE(称为AE9a)中引入了两个点突变,这些突变破坏了AML1/CBFβ相互作用(AE9aNT)。我们报告,AE9a介导的AML1靶基因异常表达不需要AE9a/CBFβ相互作用,而Notch靶基因的上调/去抑制确实需要与CBFβ相互作用。利用逆转录病毒转导在小鼠成年骨髓来源的造血祖细胞中表达AE9a,我们观察到AE9a和AE9aNT在体内均导致骨髓增殖增加。然而,只有AE9a能观察到白血病的发生和长期再增殖能力,而AE9aNT则不能。因此,AE9a驱动的白血病发生需要AML1和Notch靶基因的失调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4625/5668496/9061ce0746b6/leu2017105f1.jpg

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