Barr F G, Sellinger B, Emanuel B S
Division of Human Genetics and Molecular Biology, Children's Hospital of Philadelphia, Pennsylvania 19104.
Genomics. 1991 Dec;11(4):941-7. doi: 10.1016/0888-7543(91)90018-a.
Previous investigations of the pediatric soft tissue tumor alveolar rhabdomyosarcoma have identified a characteristic translocation t(2;13)(q35;q14). We have employed a physical mapping strategy to localize the site of this translocation breakpoint on chromosome 13. Using a panel of somatic cell hybrid and lymphoblast cell lines with deletions and unbalanced translocations involving chromosome 13, we have mapped numerous probes from the 13q12-q14 region and demonstrate that this region is divisible into five physical intervals. These probes were then mapped with respect to the t(2;13) rhabdomyosarcoma breakpoint by quantitative Southern blot analysis of an alveolar rhabdomyosarcoma cell line with two copies of the derivative chromosome 13 and one copy of the derivative chromosome 2. Our findings demonstrate that the t(2;13) breakpoint is localized within a map interval delimited by the proximal deletion breakpoints in lymphoblast lines GM01484 and GM07312. Furthermore, the breakpoint is most closely flanked by loci D13S29 and TUBBP2 within this map interval. These findings will facilitate chromosomal walking strategies for cloning the regions disrupted by the alveolar rhabdomyosarcoma translocation. In addition, this physical map will permit rapid determination of the proximity of new cloned sequences to the translocation breakpoint.
以往对儿童软组织肿瘤肺泡横纹肌肉瘤的研究已确定其具有特征性的t(2;13)(q35;q14)易位。我们采用了一种物理图谱策略来定位13号染色体上该易位断点的位置。利用一组具有涉及13号染色体缺失和不平衡易位的体细胞杂种和淋巴母细胞系,我们对来自13q12 - q14区域的众多探针进行了定位,并证明该区域可分为五个物理区间。然后,通过对具有两条衍生13号染色体和一条衍生2号染色体的肺泡横纹肌肉瘤细胞系进行定量Southern印迹分析,将这些探针相对于t(2;13)横纹肌肉瘤断点进行定位。我们的研究结果表明,t(2;13)断点位于由淋巴母细胞系GM01484和GM07312中的近端缺失断点所界定的图谱区间内。此外,在该图谱区间内,断点最靠近基因座D13S29和TUBBP2。这些发现将有助于采用染色体步移策略克隆被肺泡横纹肌肉瘤易位破坏的区域。此外,这一物理图谱将允许快速确定新克隆序列与易位断点的接近程度。