Varley H, Di S, Scherer S W, Royle N J
Department of Genetics, University of Leicester, Leicester, LE1 7RH, United Kingdom.
Am J Hum Genet. 2000 Sep;67(3):610-22. doi: 10.1086/303050. Epub 2000 Aug 1.
We have developed a strategy for the isolation of terminal deletion breakpoints from any chromosome that has been healed by de novo addition of a telomere repeat array. Breakpoints at 7q32 and 22q13.3 have been isolated and characterized in two patients (patients FB336R and AJ). Both truncated chromosomes have been healed by the addition of a novel telomere, with such an addition possibly mediated by the enzyme telomerase. The breakpoint at 7q32 in patient FB336R shows a structure similar to that of breakpoints on other chromosomes that have been healed in this way. However, the breakpoint at 22q13.3 in patient AJ has 10 nucleotides of unknown origin inserted between the sequence unique to chromosome 22q and the start of the telomere repeat array. This unusual structure is suggestive of a multistep healing event resulting in de novo telomere addition at this breakpoint, and possible mechanisms are discussed.
我们已经开发出一种策略,用于从任何通过端粒重复序列阵列的从头添加而愈合的染色体中分离末端缺失断点。在两名患者(患者FB336R和AJ)中分离并鉴定了7q32和22q13.3处的断点。两条截短的染色体都通过添加新的端粒而愈合,这种添加可能由端粒酶介导。患者FB336R中7q32处的断点显示出与以这种方式愈合的其他染色体上的断点相似的结构。然而,患者AJ中22q13.3处的断点在22q染色体特有的序列与端粒重复序列阵列的起始之间插入了10个来源不明的核苷酸。这种不寻常的结构提示了一个多步骤的愈合事件,导致在此断点处从头添加端粒,并讨论了可能的机制。