Marculescu R, Le T, Böcskör S, Mitterbauer G, Chott A, Mannhalter C, Jaeger U, Nadel B
Department of Internal Medicine I, Division of Hematology, University of Vienna, Vienna, Austria.
Leukemia. 2002 Jan;16(1):120-6. doi: 10.1038/sj.leu.2402324.
T(14;18) chromosomal translocation is assumed to result from illegitimate rearrangement between the BCL2 proto-oncogene and the IGH locus during the D(H) to J(H) joining phase of V(D)J recombination in early B cells. Analysis of the breakpoint junctions suggests that translocation derives from the fusion between normal V(D)J recombination intermediates at the IGH locus and non-V(D)J-mediated broken-ends at the BCL2 locus. So far, BCL2 broken-ends have only been observed fused to coding-ends, raising questions concerning the molecular constraints of the illegitimate joining process. Using a combination of genome walking and long-range PCR assays, we describe in this report that in 4.5% (2/44) of the t(14;18), one of the BCL2 broken-ends is fused to a signal-end. The formation of these J(H)RSS/BCL2 junctions provides direct evidence that BCL2 broken-ends are capable of joining to both products of V(D)J recombination, suggesting their presence in the RAG-mediated post-cleavage complex. In addition, junctions generated by this alternative end-joining do not involve deletion of the chromosome 14 intervening sequences generally lost in the standard translocation, providing a unique opportunity to investigate the rearrangement status of this region in the translocated IGH allele. In both cases, a DJ(H) rearrangement could be detected 5' of the J(H)-RSS/BCL2 junction. These findings, together with the previously reported bias towards the most external D(H) and J(H) segments in standard breakpoints, strongly suggest that t(14;18) preferentially occurs during an attempted secondary D(H) to J(H) rearrangement. This unusual and restricted window of differentiation opens intriguing questions concerning the etiology of the translocation.
T(14;18)染色体易位被认为是早期B细胞V(D)J重组的D(H)到J(H)连接阶段,BCL2原癌基因与IGH基因座之间发生非法重排的结果。对断点连接的分析表明,易位源于IGH基因座正常V(D)J重组中间体与BCL2基因座非V(D)J介导的断裂末端之间的融合。到目前为止,仅观察到BCL2断裂末端与编码末端融合,这引发了关于非法连接过程分子限制的问题。本报告中,我们通过基因组步移和长距离PCR检测相结合的方法,发现在4.5%(2/44)的t(14;18)中,BCL2的一个断裂末端与一个信号末端融合。这些J(H)RSS/BCL2连接的形成提供了直接证据,表明BCL2断裂末端能够与V(D)J重组的两种产物连接,提示它们存在于RAG介导的切割后复合物中。此外,这种替代末端连接产生的连接不涉及标准易位中通常缺失的14号染色体中间序列的缺失,为研究易位IGH等位基因中该区域的重排状态提供了独特机会。在这两种情况下,都可以在J(H)-RSS/BCL2连接的5'端检测到DJ(H)重排。这些发现,连同先前报道的标准断点中对最外部D(H)和J(H)片段的偏向性,强烈表明t(14;18)优先发生在尝试的二次D(H)到J(H)重排过程中。这种不寻常且受限的分化窗口引发了关于易位病因的有趣问题。