Sacchi N, Schiaffonati L, Magnani I, Pappalardo C, Hughes A J, Darfler M, Hoogeveen A T
Department of Biology and Genetics, Medical School, University of Milan, Italy.
Oncogene. 1996 Jan 18;12(2):437-44.
AML1, a gene encoding a protein of the PEBP2/CBF family of transcription factors is disrupted by translocations associated with human leukemia. In the t(8;21) acute myelogenous leukemia (AML), AML1 was found fused to a gene on chromosome 8 that we designated CDR (also known as ETO and MTG8). Immunoprecipitation experiments followed by immunoblotting using a combination of antibodies against different epitopes of one of the predicted chimeric proteins encoded by a fully characterized fusion transcript enabled us to visualize a chimeric protein in the t(8;21) Kasumi-1 cell line. The estimated size of this protein is 64 kDa. Immunoblotting of leukemic blasts containing the t(8;21) detected a protein of the same size. Immunofluorescence experiments indicate that the chimeric protein is localized in the nucleus. A normal AML1 protein of 27 kDa was also detected in t(8;21) Kasumi-1 cells. It remains to be established by which mechanism the mutant AML1 isoform may contribute to the leukemogenesis process of t(8;21)-positive acute myeloid leukemia.
AML1是一种编码转录因子PEBP2/CBF家族蛋白的基因,它会因与人类白血病相关的易位而被破坏。在t(8;21)急性髓性白血病(AML)中,发现AML1与8号染色体上的一个基因融合,我们将该基因命名为CDR(也称为ETO和MTG8)。通过使用针对由一个完全表征的融合转录本编码的一种预测嵌合蛋白的不同表位的抗体组合进行免疫沉淀实验,随后进行免疫印迹,使我们能够在t(8;21) Kasumi-1细胞系中可视化一种嵌合蛋白。这种蛋白的估计大小为64 kDa。对含有t(8;21)的白血病原始细胞进行免疫印迹检测到相同大小的一种蛋白。免疫荧光实验表明嵌合蛋白定位于细胞核中。在t(8;21) Kasumi-1细胞中也检测到了27 kDa的正常AML1蛋白。突变的AML1异构体可能通过何种机制促成t(8;21)阳性急性髓性白血病的白血病发生过程仍有待确定。