Komatsu H, Iida S, Yamamoto K, Mikuni C, Nitta M, Takahashi T, Ueda R, Seto M
Laboratory of Chemotherapy, Aichi Cancer Center Research Institute, Nagoya, Japan.
Blood. 1994 Aug 15;84(4):1226-31.
The 11q13 breakpoint region of t(11;14) (q13;q32), translocated to the Ig heavy chain locus at 14q32, has been designated as BCL-1 for B-cell leukemia/lymphoma-1, but the nature of the transcriptional unit has long remained unclear. Recently, the PRAD1 gene encoding cyclin D1, isolated from the 11q13 region, was proposed as a candidate BCL-1 gene on the basis of chromosome walking and concordant overexpression of PRAD1 mRNA in cell lines with t(11;14)(q13;q32). We report here molecular analysis of a variant translocation at the BCL-1 locus, t(11;22)(q13;q11), showing juxtaposition of the Ig light chain gene, Ig lambda, to the PRAD1 gene at its 3' end, resulting in overexpression of PRAD1 mRNA. Because only the PRAD1 gene is present between the Ig heavy chain and light chain gene breakpoints, an identity between BCL-1 and the PRAD1/cyclin D1 gene is strongly indicated.
在t(11;14)(q13;q32)中,11q13断点区域易位至14q32的免疫球蛋白重链基因座,被指定为B细胞白血病/淋巴瘤1(BCL-1),但其转录单位的性质长期以来一直不清楚。最近,从11q13区域分离出的编码细胞周期蛋白D1的PRAD1基因,基于染色体步移以及PRAD1 mRNA在伴有t(11;14)(q13;q32)的细胞系中的一致性过表达,被提议作为候选BCL-1基因。我们在此报告对BCL-1基因座处一个变异易位t(11;22)(q13;q11)的分子分析,该易位显示免疫球蛋白轻链基因Igλ在其3'端与PRAD1基因并列,导致PRAD1 mRNA过表达。由于在免疫球蛋白重链和轻链基因断点之间仅存在PRAD1基因,强烈提示BCL-1与PRAD1/细胞周期蛋白D1基因相同。