Park V M, Gustashaw K M, Wathen T M
Genetics Center, Department of Pediatrics, Case Western Reserve University, Cleveland, OH 44106.
Am J Hum Genet. 1992 May;50(5):914-23.
We describe a novel chromosome structure in which telomeric sequences are present interstitially, at the apparent breakpoint junctions of structurally abnormal chromosomes. In the linear chromosomes with interstitial telomeric sequences, there were three sites of hybridization of the telomere consensus sequence within each derived chromosome: one at each terminus and one at the breakpoint junction. Telomeric sequences also were observed within a ring chromosome. The rearrangements examined were constitutional chromosome abnormalities with a breakpoint assigned to a terminal band. In each case (with the exception of the ring chromosome), an acentric segment of one chromosome was joined to the terminus of an apparently intact recipient chromosome. One case exhibited apparent instability of the chromosome rearrangement, resulting in somatic mosaicism. The rearrangements described here differ from the telomeric associations observed in certain tumors, which appear to represent end-to-end fusion of two or more intact chromosomes. The observed interstitial telomeric sequences appear to represent nonfunctional chromosomal elements, analogous to the inactivated centromeres observed in dicentric chromosomes.
我们描述了一种新型染色体结构,其中端粒序列间隙性地存在于结构异常染色体的明显断点连接处。在带有间隙端粒序列的线性染色体中,每个衍生染色体内部存在三个端粒共有序列杂交位点:两端各一个,断点连接处一个。在环状染色体中也观察到了端粒序列。所检测的重排是染色体结构异常,断点定位于末端带。在每种情况下(环状染色体除外),一条染色体的无着丝粒片段与一条明显完整的受体染色体的末端相连。有一例表现出染色体重排明显不稳定,导致体细胞嵌合体。这里描述的重排不同于在某些肿瘤中观察到的端粒关联,后者似乎代表两个或更多完整染色体的端对端融合。观察到的间隙端粒序列似乎代表无功能的染色体元件,类似于在双着丝粒染色体中观察到的失活着丝粒。