Takahashi Y, Fujita H, Nakamura Y, Kurahashi H
Department of Medical Genetics, Osaka University Medical School, Japan.
Jpn J Hum Genet. 1997 Dec;42(4):517-23. doi: 10.1007/BF02767028.
We investigated six Robertsonian translocations, including two cases of rob(13q14q); one of rob(14q21q), one of rob (13q22q), and two of rob(21q21q), by means of fluorescence in situ hybridization (FISH) using five repetitive DNA probes: two alpha-satellite DNAs (D21Z1/D13Z1 and D14Z1/D22Z1), satellite III DNA, beta-satellite DNA, and ribosomal DNA. Single color FISH successfully defined the breakpoints in four cases of the six. Since the remaining two cases, rob(13q22q) and rob(21q21q), revealed to retain rDNA, we tried to define the breakpoints in detail by dual color FISH in these rare types. In the rob(13q22q) the chromosomal breakage on chromosome 22 was likely to have occurred within the rDNA region and that the chromosome 13 breakpoint was within the alpha-satellite region. In one rob(21q21q) case we defined the breakpoint on one chromosome distal to, or within, the beta-satellite region distal to the rDNA, and the other chromosome breakage had occurred within alpha-satellite DNA. Our results underscored the power of dual-color FISH for defining the precise locations of breakpoints in Robertsonian translocations.
我们通过荧光原位杂交(FISH),使用五种重复DNA探针:两种α-卫星DNA(D21Z1/D13Z1和D14Z1/D22Z1)、卫星III DNA、β-卫星DNA和核糖体DNA,对六例罗伯逊易位进行了研究,其中包括两例rob(13q14q);一例rob(14q21q),一例rob(13q22q),以及两例rob(21q21q)。单色FISH成功确定了六例中的四例的断点。由于其余两例,即rob(13q22q)和rob(21q21q),显示保留了rDNA,我们试图通过双色FISH在这些罕见类型中详细确定断点。在rob(13q22q)中,22号染色体上的染色体断裂可能发生在rDNA区域内,而第13号染色体的断点在α-卫星区域内。在一例rob(21q21q)中,我们确定了一条染色体上的断点位于rDNA远端的β-卫星区域远端或该区域内,而另一条染色体的断裂发生在α-卫星DNA内。我们的结果强调了双色FISH在确定罗伯逊易位中断点精确位置方面的作用。