Macera M J, Szabo P, Lin J H, DeSalvo A T, Shah H O, Verma R S
Long Island College Hospital-SUNY Health Science Center at Brooklyn 11201.
Genes Chromosomes Cancer. 1993 Oct;8(2):127-30. doi: 10.1002/gcc.2870080210.
In a small percentage of cases of chronic myelogenous leukemia (CML), where the Ph chromosome is masked because of highly complex translocations and sub-microscopic rearrangements, precise identification of chromosomal aberrations by routine banding techniques has been difficult. We report on a new case of CML in which a single copy of a masked Ph chromosome was duplicated during blast crisis, i.e., the karyotype was 47,XY,dir ins(22;9)(q11;q34.1q34.2),t(1;22) (q21;q11), + der (22)t(1;22)(q21;q11). The chromosome in situ suppression hybridization (CISS) technique with whole chromosome 1 and 22 specific painting probes demonstrated that 22q11-qter had been translocated to 1q21, whereas 22q11 was the recipient of 1q21-qter. Furthermore, a cosmid probe identified the location of the ABL gene on only one chromosome 9 (band q34). The other ABL gene could be detected on both derivative chromosomes 22 at band q11 which was flanked by the translocated part of the long arm of chromosome 1, thus providing direct visualization of the ABL insertion in a double masked Ph chromosome. A breakpoint within the 5.8 kb major breakpoint cluster [M-BCR] region was shown by Southern blotting.
在一小部分慢性粒细胞白血病(CML)病例中,由于高度复杂的易位和亚显微重排,Ph染色体被掩盖,通过常规显带技术精确识别染色体畸变一直很困难。我们报告了一例新的CML病例,其中一条被掩盖的Ph染色体单拷贝在急变期发生了复制,即核型为47,XY,dir ins(22;9)(q11;q34.1q34.2),t(1;22) (q21;q11), + der (22)t(1;22)(q21;q11)。使用1号和22号染色体特异性全染色体涂染探针的染色体原位抑制杂交(CISS)技术表明,22q11-qter已易位至1q21,而22q11是1q21-qter的接受者。此外,一个黏粒探针仅在一条9号染色体(q34带)上确定了ABL基因的位置。另一个ABL基因可在两条衍生的22号染色体的q11带检测到,该带两侧是1号染色体长臂的易位部分,从而直接显示了ABL基因在双掩盖Ph染色体中的插入情况。Southern印迹法显示在5.8 kb主要断裂点簇[M-BCR]区域内存在一个断裂点。