Hutchison/MRC Research Centre and Department of Pathology, University of Cambridge, Cambridge, UK.
Genome Res. 2011 Apr;21(4):525-34. doi: 10.1101/gr.114116.110. Epub 2011 Jan 20.
Reciprocal chromosome translocations are often not exactly reciprocal. Most familiar are deletions at the breakpoints, up to megabases in extent. We describe here the opposite phenomenon-duplication of tens or hundreds of kilobases at the breakpoint junction, so that the same sequence is present on both products of a translocation. When the products of the translocation are mapped on the genome, they overlap. We report several of these "overlapping-breakpoint" duplications in breast cancer cell lines HCC1187, HCC1806, and DU4475. These lines also had deletions and essentially balanced translocations. In HCC1187 and HCC1806, we identified five cases of duplication ranging between 46 kb and 200 kb, with the partner chromosome showing deletions between 29 bp and 31 Mb. DU4475 had a duplication of at least 200 kb. Breakpoints were mapped using array painting, i.e., hybridization of chromosomes isolated by flow cytometry to custom oligonucleotide microarrays. Duplications were verified by fluorescent in situ hybridization (FISH), PCR on isolated chromosomes, and cloning of breakpoints. We propose that these duplications are the counterpart of deletions and that they are produced at a replication bubble, comprising two replication forks with the duplicated sequence in between. Both copies of the duplicated sequence would go to one daughter cell, on different products of the translocation, while the other daughter cell would show deletion. These duplications may have been overlooked because they may be missed by FISH and array-CGH and may be interpreted as insertions by paired-end sequencing. Such duplications may therefore be quite frequent.
相互易位染色体通常不是完全相互的。最常见的是在断点处缺失,多达兆碱基。我们在这里描述了相反的现象-在断点连接处重复数十或数百千碱基,使得相同的序列存在于易位的两个产物上。当易位的产物映射到基因组上时,它们会重叠。我们在乳腺癌细胞系 HCC1187、HCC1806 和 DU4475 中报告了几个这样的“重叠断点”重复。这些系也有缺失和基本平衡的易位。在 HCC1187 和 HCC1806 中,我们鉴定了五个重复范围在 46kb 到 200kb 之间的案例,与伙伴染色体之间的缺失范围在 29bp 到 31Mb 之间。DU4475 至少有 200kb 的重复。使用阵列绘画(即通过流式细胞术分离的染色体与定制寡核苷酸微阵列杂交)来定位断点。通过荧光原位杂交(FISH)、分离染色体上的 PCR 和断点克隆来验证重复。我们提出这些重复是缺失的对应物,它们是在复制泡中产生的,复制泡包含两个复制叉,中间有重复的序列。重复序列的两个副本都将进入一个子细胞,在易位的不同产物上,而另一个子细胞将显示缺失。这些重复可能被忽略了,因为它们可能会错过 FISH 和阵列-CGH,并且可能被配对末端测序解释为插入。因此,这样的重复可能相当频繁。