Jeffs A R, Wells E, Morris C M
Leukaemia Research Group, Christchurch School of Medicine, Christchurch, New Zealand.
Genes Chromosomes Cancer. 2001 Oct;32(2):144-54. doi: 10.1002/gcc.1176.
The Philadelphia translocation, t(9;22)(q34;q11), is the microscopically visible product of recombination between two genes, ABL1 on chromosome 9 and BCR on chromosome 22, and gives rise to a functional hybrid BCR-ABL1 gene with demonstrated leukemogenic properties. Breakpoints in BCR occur mostly within one of two regions: a 5 kb major breakpoint cluster region (M-Bcr) and a larger 35 kb minor breakpoint cluster region (m-Bcr) towards the 3' end of the first BCR intron. By contrast, breakpoints in ABL1 are reported to occur more widely across a >200 kb region which spans the large first and second introns. The mechanisms that determine preferential breakage sites in BCR, and which cause recombination between BCR and ABL1, are presently unknown. In some cases, Alu repeats have been identified at or near sequenced breakpoint sites in both genes, providing indications, albeit controversial, that they may be relevant. For the present study, we carried out a detailed analysis of genomic BCR and ABL1 sequences to identify, classify, and locate interspersed repeat sequences and to relate their distribution to precisely mapped BCR-ABL1 recombination sites. Our findings confirm that Alu are the most abundant class of repeat in both genes, but that they occupy fewer sites than previously estimated and that they are distributed nonrandomly. r-Scan statistics were applied to provide a measure of repeat distribution and to evaluate extremes in repeat spacing. A significant lack of Alu elements was observed across the major and minor breakpoint cluster regions of BCR and across a 25-kb region showing a high frequency of breakage in ABL1. These findings counter the suggestion that occurrence of Alu at BCR-ABL1 recombination sites is likely by chance because of the high density of Alu in these two genes. Instead, as yet unidentified DNA conformation or nucleotide characteristics peculiar to the preferentially recombining regions, including those Alu elements present within them, more likely influence their fragility.
费城染色体易位,t(9;22)(q34;q11),是9号染色体上的ABL1基因与22号染色体上的BCR基因之间重组的微观可见产物,可产生具有白血病生成特性的功能性杂种BCR-ABL1基因。BCR的断点大多出现在两个区域之一:一个5 kb的主要断点簇区域(M-Bcr)和一个更大的35 kb的次要断点簇区域(m-Bcr),位于第一个BCR内含子的3'端。相比之下,ABL1的断点据报道在跨越>200 kb区域(跨越较大的第一个和第二个内含子)的范围内更广泛地出现。目前尚不清楚决定BCR中优先断裂位点以及导致BCR与ABL1之间重组的机制。在某些情况下,在两个基因的测序断点位点处或附近已鉴定出Alu重复序列,这表明它们可能相关,尽管存在争议。在本研究中,我们对基因组BCR和ABL1序列进行了详细分析,以识别、分类和定位散布的重复序列,并将它们的分布与精确映射的BCR-ABL1重组位点相关联。我们的研究结果证实,Alu是这两个基因中最丰富的重复序列类别,但它们占据的位点比先前估计的要少,并且它们的分布是非随机的。应用r-Scan统计来衡量重复序列分布并评估重复序列间距的极端情况。在BCR的主要和次要断点簇区域以及ABL1中显示高断裂频率的25 kb区域中,观察到Alu元件明显缺乏。这些发现反驳了由于这两个基因中Alu的高密度,Alu在BCR-ABL1重组位点出现可能是偶然的这一观点。相反,优先重组区域特有的尚未确定的DNA构象或核苷酸特征,包括其中存在的那些Alu元件,更有可能影响它们的脆性。