Sacchi N, Watson D K, Guerts van Kessel A H, Hagemeijer A, Kersey J, Drabkin H D, Patterson D, Papas T S
Science. 1986 Jan 24;231(4736):379-82. doi: 10.1126/science.3941901.
Human probes identifying the cellular homologs of the v-ets gene, Hu-ets-1 and Hu-ets-2, and two panels of rodent-human cell hybrids were used to study specific translocations occurring in acute leukemias. The human ets-1 gene was found to translocate from chromosome 11 to 4 in the t(4;11)(q21;23), a translocation characteristic of a subtype of leukemia that represents the expansion of a myeloid/lymphoid precursor cell. Similarly, the human ets-2 gene was found to translocate from chromosome 21 to chromosome 8 in the t(8;21)(q22;q22), a nonrandom translocation commonly found in patients with acute myeloid leukemia with morphology M2 (AML-M2). Both translocations are associated with expression different from the expression in normal lymphoid cells of ets genes, raising the possibility that these genes play a role in the pathogenesis of these leukemias.
利用鉴定v-ets基因细胞同源物Hu-ets-1和Hu-ets-2的人类探针以及两组啮齿动物-人类细胞杂交体,研究急性白血病中发生的特异性易位。发现在t(4;11)(q21;23)中,人类ets-1基因从11号染色体易位至4号染色体,该易位是一种白血病亚型的特征,代表髓系/淋巴系前体细胞的扩增。同样,发现在t(8;21)(q22;q22)中,人类ets-2基因从21号染色体易位至8号染色体,这是一种在形态学为M2的急性髓系白血病(AML-M2)患者中常见的非随机易位。这两种易位均与ets基因在正常淋巴细胞中的表达不同,提示这些基因可能在这些白血病的发病机制中发挥作用。