Moulding C, Rapoport A, Goldman P, Battey J, Lenoir G M, Leder P
Nucleic Acids Res. 1985 Mar 25;13(6):2141-52. doi: 10.1093/nar/13.6.2141.
The balanced translocations that occur between the c-myc and immunoglobulin loci in Burkitt lymphoma provide an unusual opportunity to analyze both products of a reciprocal recombination. Accordingly, we have determined the structure of the two reciprocal products of a translocation that joins the 5' portion of the c-myc gene on chromosome 8 to the immunoglobulin mu switch recombination signal on chromosome 14. By determining the nucleotide sequences at the translocation crossover points of both product chromosomes, we precisely locate these points with respect to nearby genes. This determination allows us to conclude that translocation involves nonhomologous recombination, is highly conservative of c-myc sequences (deleting only 16 bp at the crossover point), but deletes over 2 Kb of immunoglobulin sequences from the mu switch signal. The mu constant and c-myc genes are joined head-to-head about 3 Kb apart, while the IgH enhancer and an aberrantly rearranged D/J region are linked to sequences 5' of c-myc on the reciprocal product.
伯基特淋巴瘤中c-myc与免疫球蛋白基因座之间发生的平衡易位为分析相互重组的两种产物提供了一个特殊的机会。因此,我们确定了一种易位的两个相互产物的结构,该易位将8号染色体上c-myc基因的5'部分与14号染色体上的免疫球蛋白μ转换重组信号连接起来。通过确定两个产物染色体易位交叉点处的核苷酸序列,我们相对于附近的基因精确地定位了这些点。这一确定使我们能够得出结论,易位涉及非同源重组,对c-myc序列高度保守(在交叉点仅缺失16 bp),但从μ转换信号中删除了超过2 Kb的免疫球蛋白序列。μ恒定区和c-myc基因以头对头的方式连接,相距约3 Kb,而IgH增强子和异常重排的D/J区域与相互产物上c-myc的5'端序列相连。