Liu Hongxiang, Hamoudi Rifat A, Ye Hongtao, Ruskone-Fourmestraux Agnes, Dogan Ahmet, Isaacson Peter G, Du Ming-Qing
Department of Pathology, University of Cambridge, Cambridge, UK.
Br J Haematol. 2004 May;125(3):318-29. doi: 10.1111/j.1365-2141.2004.04909.x.
t(11;18)(q21;q21) is the most frequent chromosomal aberration specifically associated with mucosa-associated lymphoid tissue (MALT) lymphoma. The translocation fuses the API2 gene to the MALT1 gene and generates a functional API2-MALT1 transcript. The breakpoint of the fusion gene is well characterized at the transcript level but poorly understood at the genomic level and the mechanism underlying the translocation is unknown. We identified the genomic breakpoint in 19 t(11;18)-positive MALT lymphoma cases by polymerase chain reaction and sequencing and analysed the junctional sequences. The breakpoints were scattered in intron 7 and exon 8 of the API2 gene, and introns 4, 6, 7 and 8 of the MALT1 gene. Comparative sequence analysis between the API2-MALT1 fusion on der(11) and the MALT1-API2 fusion on der(18) showed extensive alterations including deletions, duplications and non-template-based insertions at the fusion junctions in all cases examined. An extensive sequence search failed to reveal any known sequence motifs that might be associated with chromosomal recombination or any novel consensus sequences at or near the breakpoints on both der(11) and der(18) except in one case, in which Alu repeats spanned the breakpoint of the MALT1-API2 fusion. Our results suggest that t(11;18) may result from illegitimate non-homologous end joining following double strand breaks.
t(11;18)(q21;q21)是与黏膜相关淋巴组织(MALT)淋巴瘤特异性相关的最常见染色体畸变。该易位将API2基因与MALT1基因融合,并产生功能性的API2-MALT1转录本。融合基因的断点在转录水平上已得到很好的表征,但在基因组水平上了解甚少,且易位的潜在机制尚不清楚。我们通过聚合酶链反应和测序确定了19例t(11;18)阳性MALT淋巴瘤病例中的基因组断点,并分析了连接序列。断点分散在API2基因的第7内含子和第8外显子以及MALT1基因的第4、6、7和8内含子中。对der(11)上的API2-MALT1融合与der(18)上的MALT1-API2融合进行的比较序列分析显示,在所有检测的病例中,融合连接处都有广泛的改变,包括缺失、重复和非模板插入。广泛的序列搜索未能揭示任何可能与染色体重组相关的已知序列基序,也未揭示der(11)和der(18)断点处或附近的任何新的共有序列,只有一个病例除外,其中Alu重复序列跨越了MALT1-API2融合的断点。我们的结果表明,t(11;18)可能是由双链断裂后的非法非同源末端连接导致的。