Tanaka K, Tanaka T, Ogawa S, Kurokawa M, Mitani K, Yazaki Y, Hirai H
Third Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
Biochem Biophys Res Commun. 1995 Jun 26;211(3):1023-30. doi: 10.1006/bbrc.1995.1913.
The AML1 gene on chromosome 21 is disrupted in the (8;21)(q22;q22) and (3;21)(q26;q22) translocations associated with myelogenous leukemias and encodes a DNA binding protein. From the AML1 gene, three proteins, AML1a, AML1b and AML1c, are produced by alternative splicings. We previously showed that AML1 is potentially involved in myeloid cell differentiation. Here we analyzed the expression of AML1 in myeloid cell lines. It was revealed that AML1b and AML1c are the major AML1 proteins in these cell lines and that prior to morphological and functional differentiation, their expressions increase in U937 cells when treated with all-trans retinoic acid. These data suggest that the expression of AML1 is associated with myeloid cell differentiation.
21号染色体上的AML1基因在与骨髓性白血病相关的(8;21)(q22;q22)和(3;21)(q26;q22)易位中发生破坏,并编码一种DNA结合蛋白。从AML1基因中,通过可变剪接产生三种蛋白质,AML1a、AML1b和AML1c。我们先前表明AML1可能参与髓细胞分化。在此我们分析了AML1在髓细胞系中的表达。结果显示AML1b和AML1c是这些细胞系中的主要AML1蛋白,并且在形态和功能分化之前,用全反式维甲酸处理时,它们在U937细胞中的表达增加。这些数据表明AML1的表达与髓细胞分化相关。