Morishita K, Parganas E, William C L, Whittaker M H, Drabkin H, Oval J, Taetle R, Valentine M B, Ihle J N
Department of Biochemistry, St. Jude Children's Research Hospital, Memphis, TN 38105.
Proc Natl Acad Sci U S A. 1992 May 1;89(9):3937-41. doi: 10.1073/pnas.89.9.3937.
Retroviral activation of Evi-1 gene expression is one of the most common transforming events in murine myeloid leukemias. To evaluate the role of the EVI1 gene in human acute myelogenous leukemia (AML), leukemic blasts or cell lines from 116 patients were examined. In eight patients the EVI1 gene was expressed and all but one had cytogenetically detectable translocations of chromosome 3q26 where the EVI1 gene has been localized. To identify breakpoints, a restriction map that spans 1700 kilobases (kb) of the EVI1 locus was developed by pulsed-field gel electrophoresis. In one case, t(3;3)(q21;q26), a rearrangement was localized to 170-330 kb 5' of the gene. In a second case, t(3;3)(q21;q26), there was a rearrangement 13 kb 5' of the gene. This rearrangement was cloned and shown to be due to the fusion of sequences from 3q21-22 with the EVI1 locus. In the third case, ins(3)-(q21q25q27), there was a rearrangement that mapped 150 kb downstream from the 5' end of the gene.
Evi-1基因表达的逆转录病毒激活是小鼠骨髓性白血病中最常见的转化事件之一。为评估EVI1基因在人类急性髓性白血病(AML)中的作用,对116例患者的白血病原始细胞或细胞系进行了检测。8例患者中EVI1基因表达,除1例患者外,其余所有患者在细胞遗传学上均可检测到3号染色体q26带的易位,EVI1基因定位于此。为确定断点,通过脉冲场凝胶电泳构建了跨越EVI1基因座1700千碱基(kb)的限制酶图谱。在1例t(3;3)(q21;q26)患者中,重排定位于该基因5'端上游170 - 330 kb处。在第2例t(3;3)(q21;q26)患者中,重排位于该基因5'端上游13 kb处。此重排被克隆,结果表明是3号染色体q21 - 22序列与EVI1基因座融合所致。在第3例ins(3)-(q21q25q27)患者中,重排定位于该基因5'端下游150 kb处。