Tsujimoto Y, Gorham J, Cossman J, Jaffe E, Croce C M
Science. 1985 Sep 27;229(4720):1390-3. doi: 10.1126/science.3929382.
In this study, the joining sequences between chromosomes 14 and 18 on the 14q+ chromosomes of a patient with pre-B-cell leukemia and four patients with follicular lymphoma carrying a t(14;18) chromosome translocation were analyzed. In each case, the involved segment of chromosome 18 has recombined with the immunoglobulin heavy-chain joining segment (JH) on chromosome 14. The sites of the recombination on chromosome 14 are located close to the 5' end of the involved JH segment, where the diversity (D) regions are rearranged with the JH segments in the production of active heavy-chain genes. As extraneous nucleotides (N regions) were observed at joining sites and specific signal-like sequences were detected on chromosome 18 in close proximity to the breakpoints, it is concluded that the t(14;18) chromosome translocation is the result of a mistake during the process of VDJ joining at the pre-B-cell stage of differentiation. The putative recombinase joins separated DNA segments on two different chromosomes instead of joining separated segments on the same chromosome, causing a t(14;18) chromosome translocation in the involved B cells.
在本研究中,分析了一名前B细胞白血病患者以及四名携带t(14;18)染色体易位的滤泡性淋巴瘤患者的14q+染色体上14号与18号染色体之间的连接序列。在每种情况下,18号染色体的受累片段都与14号染色体上的免疫球蛋白重链连接片段(JH)发生了重组。14号染色体上的重组位点位于受累JH片段的5'端附近,在活性重链基因的产生过程中,多样性(D)区域与JH片段在此处发生重排。由于在连接位点观察到了外来核苷酸(N区域),并且在18号染色体上靠近断点处检测到了特定的信号样序列,因此得出结论,t(14;18)染色体易位是分化前B细胞阶段VDJ连接过程中出错的结果。假定的重组酶将两条不同染色体上分离的DNA片段连接起来,而不是将同一染色体上分离的片段连接起来,从而导致受累B细胞中出现t(14;18)染色体易位。