Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Am J Med Genet A. 2010 May;152A(5):1111-26. doi: 10.1002/ajmg.a.33278.
Insertional translocations (ITs) are rare events that require at least three breaks in the chromosomes involved and thus qualify as complex chromosomal rearrangements (CCR). In the current study, we identified 40 ITs from approximately 18,000 clinical cases (1:500) using array-comparative genomic hybridization (aCGH) in conjunction with fluorescence in situ hybridization (FISH) confirmation of the aCGH findings, and parental follow-up studies. Both submicroscopic and microscopically visible IT events were detected. They were divided into three major categories: (1) simple intrachromosomal and interchromosomal IT resulting in pure segmental trisomy, (2) complex IT involving more than one abnormality, (3) deletion inherited from a parent with a balanced IT resulting in pure segmental monosomy. Of the cases in which follow-up parental studies were available, over half showed inheritance from an apparently unaffected parent carrying the same unbalanced rearrangement detected in the propositi, thus decreasing the likelihood that these IT events are clinically relevant. Nevertheless, we identified six cases in which small submicroscopic events were detected involving known disease-associated genes/genomic segments and are likely to be pathogenic. We recommend that copy number gains detected by clinical aCGH analysis should be confirmed using FISH analysis whenever possible in order to determine the physical location of the duplicated segment. We hypothesize that the increased use of aCGH in the clinic will demonstrate that IT occurs more frequently than previously considered but can identify genomic rearrangements with unclear clinical significance.
插入易位(ITs)是罕见的事件,需要涉及的染色体至少有三个断裂,因此被认为是复杂的染色体重排(CCR)。在当前的研究中,我们使用了阵列比较基因组杂交(aCGH)结合荧光原位杂交(FISH)来确认 aCGH 的发现,并进行了父母随访研究,从大约 18000 例临床病例(1:500)中鉴定出了 40 个 ITs。我们检测到了亚微观和微观可见的 IT 事件。它们分为三大类:(1)简单的染色体内和染色体间 IT,导致纯片段三体;(2)涉及多个异常的复杂 IT;(3)从携带与先证者相同不平衡重排的看似正常的父母遗传的缺失,导致纯片段单体。在有后续父母研究的病例中,超过一半的病例显示来自一个明显未受影响的父母遗传了同样的不平衡重排,这降低了这些 IT 事件具有临床相关性的可能性。然而,我们发现了六个病例,其中检测到了小的亚微观事件,涉及已知的与疾病相关的基因/基因组片段,可能具有致病性。我们建议,临床 aCGH 分析检测到的拷贝数增益应尽可能通过 FISH 分析进行确认,以确定重复片段的物理位置。我们假设,临床中使用 aCGH 的增加将表明 IT 的发生频率比以前认为的要高,但可以识别出具有不明确临床意义的基因组重排。