Lemieux N, Apiou F, Vogt N, Malfoy B, Dutrillaux B
Départment de Pathologie, Faculté de Médecine, Université de Montréal, Québec, Canada.
Cancer Genet Cytogenet. 1996 Aug;90(1):75-9. doi: 10.1016/0165-4608(96)00061-1.
The MDA-MB-134 cell line was characterized by the presence of two homogeneously staining region (hsr) carrier chromosomes containing sequences from 8p11-p12, 11q13, and 8q24. Using fluorescence in situ hybridization, a detailed study of the organization of this chromosome has been performed. The hsr carrier chromosomes are shown to be identical and to derive from a chromosome 11, on which large segments of the long arm of chromosome 8 are translocated, forming its short arm. The hsr segment is inserted in the long arm, distally to C1NH gene. It is formed by sequences from both chromosomes 8 and 11. For the genes investigated by both methods the number of copies detected by in situ hybridization is compatible with that expected by quantification of Southern blots. In spite of its complexity, a possible mechanism of formation is proposed.
MDA-MB-134细胞系的特征是存在两条均一染色区(hsr)携带染色体,其包含来自8p11 - p12、11q13和8q24的序列。利用荧光原位杂交技术,已对该染色体的组织结构进行了详细研究。结果显示,hsr携带染色体是相同的,且源自11号染色体,8号染色体长臂的大片段易位至该染色体上,形成了其短臂。hsr片段插入到长臂中,位于C1NH基因的远端。它由8号和11号染色体的序列组成。对于通过两种方法研究的基因,原位杂交检测到的拷贝数与Southern印迹定量预期的拷贝数相符。尽管其结构复杂,但仍提出了一种可能的形成机制。