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本文引用的文献

1
Signatures of mutation and selection in the cancer genome.癌症基因组中的突变和选择特征。
Nature. 2010 Feb 18;463(7283):893-8. doi: 10.1038/nature08768.
2
Complex landscapes of somatic rearrangement in human breast cancer genomes.人类乳腺癌基因组中体细胞重排的复杂景观。
Nature. 2009 Dec 24;462(7276):1005-10. doi: 10.1038/nature08645.
3
DNA replication: prime-time looping.DNA复制:黄金时段的环化
Nature. 2009 Dec 17;462(7275):854-5. doi: 10.1038/462854a.
4
Mechanisms of change in gene copy number.基因拷贝数变化的机制。
Nat Rev Genet. 2009 Aug;10(8):551-64. doi: 10.1038/nrg2593.
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Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.罕见的致病性微缺失和串联重复是由局部基因组结构介导的微同源性并受其刺激产生的。
Hum Mol Genet. 2009 Oct 1;18(19):3579-93. doi: 10.1093/hmg/ddp306. Epub 2009 Jul 3.
6
A microhomology-mediated break-induced replication model for the origin of human copy number variation.一种关于人类拷贝数变异起源的微同源性介导的断裂诱导复制模型。
PLoS Genet. 2009 Jan;5(1):e1000327. doi: 10.1371/journal.pgen.1000327. Epub 2009 Jan 30.
7
Tandem duplication producing a novel oncogenic BRAF fusion gene defines the majority of pilocytic astrocytomas.串联重复产生一种新的致癌性BRAF融合基因,这在大多数毛细胞型星形细胞瘤中都有体现。
Cancer Res. 2008 Nov 1;68(21):8673-7. doi: 10.1158/0008-5472.CAN-08-2097.
8
Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13).表型正常个体断点连接区的意外复杂性以及产生平衡易位t(1;22)(p36;q13)的相关机制。
Genome Res. 2008 Nov;18(11):1733-42. doi: 10.1101/gr.077453.108. Epub 2008 Sep 2.
9
Mechanisms of leukemia translocations.白血病易位的机制。
Curr Opin Hematol. 2008 Jul;15(4):338-45. doi: 10.1097/MOH.0b013e328302f711.
10
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing.使用全基因组大规模平行双末端测序鉴定癌症中的体细胞获得性重排。
Nat Genet. 2008 Jun;40(6):722-9. doi: 10.1038/ng.128. Epub 2008 Apr 27.

相互易位断点处的大片段重复可能是大片段缺失的对应物,可能是复制泡停滞导致的。

Large duplications at reciprocal translocation breakpoints that might be the counterpart of large deletions and could arise from stalled replication bubbles.

机构信息

Hutchison/MRC Research Centre and Department of Pathology, University of Cambridge, Cambridge, UK.

出版信息

Genome Res. 2011 Apr;21(4):525-34. doi: 10.1101/gr.114116.110. Epub 2011 Jan 20.

DOI:10.1101/gr.114116.110
PMID:21252201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3065700/
Abstract

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.

摘要

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。