Graham M, Adams J M
EMBO J. 1986 Nov;5(11):2845-51. doi: 10.1002/j.1460-2075.1986.tb04578.x.
The 2;8 variant translocation of human Burkitt's lymphomas is closely related cytogenetically to the t(6;15) of murine plasmacytomas; both involve a reciprocal exchange between the Ig kappa locus and a band region indistinguishable from that bearing the c-myc oncogene. To define their molecular relationship, we have compared cloned chromosome 8 DNA from the t(2;8) breakpoint in the human Burkitt's lymphoma JBL2 with cloned DNA from the murine pvt-1 locus, the major chromosome 15 breakpoint region in murine t(6;15). DNA sequencing and Southern blot analysis shows that these two regions are homologous. Thus the t(2;8) in JBL2 is the molecular equivalent of many murine t(6;15). The murine pvt-1 locus lies an unknown distance 3' of c-myc; analysis of DNA from several tumours with c-myc amplification reveals that pvt-1 is co-amplified in at least one case, placing pvt-1 approximately 100-500 kb 3' of c-myc. The significance of these results with respect to the role of pvt-1 in tumorigenesis is discussed.
人类伯基特淋巴瘤的2;8变异易位在细胞遗传学上与鼠浆细胞瘤的t(6;15)密切相关;两者都涉及免疫球蛋白κ轻链基因座与一个与携带c-myc癌基因的区域无法区分的带区之间的相互交换。为了确定它们的分子关系,我们将来自人类伯基特淋巴瘤JBL2中t(2;8)断点的克隆8号染色体DNA与来自鼠pvt-1基因座(鼠t(6;15)中主要的15号染色体断点区域)的克隆DNA进行了比较。DNA测序和Southern印迹分析表明这两个区域是同源的。因此,JBL2中的t(2;8)在分子水平上等同于许多鼠t(6;15)。鼠pvt-1基因座位于c-myc下游未知距离处;对几例c-myc扩增肿瘤的DNA分析显示,至少在一个病例中pvt-1是共扩增的,这表明pvt-1位于c-myc下游约100 - 500 kb处。本文讨论了这些结果对于pvt-1在肿瘤发生中作用的意义。