Reddy K S, Sulcova V
Cytogenetics, Quest Diagnostics Inc., San Juan Capistrano, CA 92690, USA. reddyk@quest diagnostics.com
Hum Genet. 1998 Jun;102(6):653-62. doi: 10.1007/s004390050758.
Variant chromosomes are polymorphic in areas that are rich in repeat sequences such as the pericentromeric regions or in the acrocentric short arm regions. The dynamic nature of these regions is evident in the polymorphisms they exhibit. In this paper three unusual variants are described: a chromosome 21 with additional material on its short arm, a chromosome 7 with an insertion in the short arm and a chromosome 2 with satellites at the end of the long arm. All three variants were shown to involve acrocentric elements using special banding techniques and fluorescence in situ hybridization. The 21 variant was found to be a tricentric with a 21 and two 15 alpha-, two classical and three acrocentric beta-satellite signals interspersed by AgNOR-positive regions. The telomeres were present at the two terminal ends. The insertion on chromosome 7 was found to be C-band positive and to contain acrocentric beta-satellite DNA. However, acrocentric alpha-satellite, classical satellite, whole-chromosome-painting or all-telomeres sequence probes did not hybridize to the insertion. The satellited region of chromosome 2 had two C-bands, a small positive all-centromeres probe signal, and two signals for the beta-satellite probe. Sandwiched between the beta-satellite sequences was an AgNOR-positive region. The telomeres were present at the two ends of the satellited chromosome 2. Chromosome 2 subtelomeric probes hybridized to the terminal ends of the short and long arm of chromosome 2. The common thread in these three variants is the involvement of acrocentric short arm elements. The acrocentric short arm elements are shown to move to other acrocentric or nonacrocentric chromosomes and relocate to both terminal and interstitial positions. The integrations are stable and heritable.
变异染色体在富含重复序列的区域具有多态性,如着丝粒周围区域或近端着丝粒短臂区域。这些区域的动态性质在它们所表现出的多态性中很明显。本文描述了三种不寻常的变异体:一条21号染色体短臂上有额外的物质,一条7号染色体短臂有插入片段,一条2号染色体长臂末端有随体。使用特殊的显带技术和荧光原位杂交显示,所有这三种变异体都涉及近端着丝粒元件。发现21号变异体是一个三着丝粒,有一个21号染色体和两个15号染色体的α卫星信号、两个经典卫星信号和三个近端着丝粒β卫星信号,被银染核仁组织区阳性区域穿插。端粒位于两个末端。发现7号染色体上的插入片段C带阳性,包含近端着丝粒β卫星DNA。然而,近端着丝粒α卫星、经典卫星、全染色体涂染或所有端粒序列探针均未与该插入片段杂交。2号染色体的随体区域有两个C带、一个小的全着丝粒阳性探针信号和两个β卫星探针信号。夹在β卫星序列之间的是一个银染核仁组织区阳性区域。端粒位于有随体的2号染色体两端。2号染色体亚端粒探针与2号染色体短臂和长臂的末端杂交。这三种变异体的共同特点是涉及近端着丝粒短臂元件。近端着丝粒短臂元件显示可移动到其他近端着丝粒或非近端着丝粒染色体,并重新定位到末端和中间位置。这些整合是稳定且可遗传的。