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bcl‐2 Translocation in Japanese B Cell Lyraphoma: Novel bcl‐2 Translocation with Immunoglobulin Heavy Chain Diversity Segment

机译:日本B细胞淋巴瘤的bcl-2易位:具有免疫球蛋白重链多样性片段的新型bcl-2易位

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摘要

Breakpoints of a lymphoma case with bcl‐2 gene rearrangement that did not show comigration of immunoglobulin (Ig) heavy chain joining (JH) fragment were cloned. Sequence analysis revealed that the translocation broke the 3 side of the Ig heavy chain diversity (DH) segment at the heptamer recombination signal and each end was ligated to the bcl‐2 locus. Since Southern blot demonstrated that both alleles of JH were rearranged, this translocation was suggested to have occurred at the step of VH‐DH, or DH‐DHJH recombination, one step later than that of DH‐Jn recombination where the common pattern of bcl‐2 rearrangement generally occurs. Cases that showed comigration with JH fragment were also studied by polymerase chain reaction with 5’bcl‐2 oligomer and 3 JH consensus anti‐sense oligomer since it has been demonstrated that bcl‐2 translocation at the major breakpoint clustering region (mbr) in American cases clusters within an about 150 bp region in the mbr. The results demonstrated that four out of five cases studied were amplified, indicating that the same clustering mechanism exists for Japanese cases. The present study, together with our previous report on Igt‐bcl‐2, indicated that bcl‐2 translocation in Japanese B cell lymphomas might occur at a later stage of B cell development, as compared with that in American cases. Less involvement of bcl‐2 in Japanese B cell lymphoma may also he in part explainable by low susceptibility to bcl‐2 rearrangement at the step of DH‐JH recombination.
机译:克隆了一个bcl-2基因重排的淋巴瘤病例的断点,该断点未显示出免疫球蛋白(Ig)重链连接(JH)片段的迁移。序列分析表明,该易位在七聚体重组信号处打破了Ig重链多样性(DH)区段的3侧,并且每个末端均连接至bcl-2基因座。由于Southern印迹表明JH的两个等位基因均已重排,因此该移位建议发生在VH-DH或DH-DHJH重组的步骤中,比DH-Jn重组的步骤晚了一步,后者是bcl-的常见模式2一般会发生重排。还通过与5'bcl-2低聚物和3 JH共有反义寡聚物的聚合酶链反应研究了显示出JH片段转移的病例,因为已经证明了在美国主要断点聚类区域(mbr)发生bcl-2易位病例聚集在mbr的约150 bp区域内。结果表明,在研究的五分之四的案例中,有四分之三被放大,表明日本案例存在相同的聚类机制。本研究与我们先前关于Igt-bcl-2的报告一起表明,与美国病例相比,日本B细胞淋巴瘤中bcl-2易位可能发生在B细胞发育的后期。 bcl-2较少参与日本B细胞淋巴瘤也可能部分是由于在DH-JH重组步骤中bcl-2重排敏感性低。

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