Shaughnessy J, Wiener F, Huppi K, Mushinski J F, Potter M
Laboratory of Genetics, National Cancer Institute, Bethesda, Maryland 20892.
Oncogene. 1994 Jan;9(1):247-53.
Oil-induced murine plasmacytomas typically carry c-myc-activating non-random reciprocal chromosomal translocations that take the form of either a T(12;15) that fuses the c-myc proto-oncogene to an immunoglobulin heavy chain switch region or a T(6;15) that juxtaposes the Pvt-1 locus, located 220 kb 3' of c-myc, to the immunoglobulin light china locus, C kappa. In this report we show that the plasmacytoma ABPC 60 harbors a novel c-myc-activating T(12;15) in which the chromosome 15 breakpoint occurs in the Pvt-1 region, resulting in the head-to-tail juxtaposition of the Pvt-1 major breakpoint cluster to the IgA switch region. Restriction mapping and nucleotide sequencing of this atypical translocation indicate that a paracentric inversion in chromosome 12 must have preceeded the translocation. This is the first example of a T(12;15) with a break 3' of the c-myc gene. The rearrangement places the 3' C alpha enhancer (3' alpha E) greater than 200 kb downstream of the c-myc promoters, however c-myc mRNA levels are similar to those observed in plasmacytomas with typical T(12;15)s that translocate 3' alpha E much closer (15-25 kb) and upstream of c-myc. The up regulation of c-myc that results from this rearrangement is thought to be brought about by the interaction of the c-myc promoters with the IgA enhancer element that has been strategically relocated into the Pvt-1 region.
油诱导的小鼠浆细胞瘤通常携带激活c-myc的非随机相互染色体易位,其形式为T(12;15),将c-myc原癌基因与免疫球蛋白重链开关区域融合,或T(6;15),将位于c-myc下游220 kb的Pvt-1基因座与免疫球蛋白轻链基因座Cκ并列。在本报告中,我们显示浆细胞瘤ABPC 60含有一种新的激活c-myc的T(12;15),其中15号染色体断点发生在Pvt-1区域,导致Pvt-1主要断点簇与IgA开关区域头对头并列。对这种非典型易位的限制性图谱分析和核苷酸测序表明,12号染色体上的臂内倒位一定先于易位发生。这是c-myc基因下游3'处出现断点的T(12;15)的首个例子。这种重排使3' Cα增强子(3'αE)位于c-myc启动子下游200 kb以上,然而c-myc mRNA水平与在典型T(12;15)易位使3'αE更靠近(15-25 kb)且位于c-myc上游的浆细胞瘤中观察到的水平相似。这种重排导致的c-myc上调被认为是由c-myc启动子与已被策略性重定位到Pvt-1区域的IgA增强子元件相互作用引起的。