Loupart M L, Walker R, Brammar W, Varley J
ICI/University Joint Laboratory, University of Leicster, UK.
Chromosome Res. 1995 Nov;3(7):410-6. doi: 10.1007/BF00713890.
Fluorescence in situ hybridization (FISH) was used to establish the copy number of chromosome 1 in a set of nine breast tumours in which the chromosome had previously been shown to have undergone a variety of rearrangements by loss of heterozygosity studies. In each case, FISH with satellite III DNA from chromosome 1q12 confirmed the results obtained by Southern hybridization. Importantly, in all five cases with rearrangements thought not to involve the centromeric region, FISH showed that the events had not disrupted the gross chromosome structure. This study highlights the potential of using the two techniques together to obtain a clearer picture of both large- and small-scale alterations to chromosomes in solid tumours.
荧光原位杂交(FISH)被用于确定一组9个乳腺肿瘤中1号染色体的拷贝数,此前通过杂合性缺失研究已表明该染色体发生了多种重排。在每种情况下,用来自1号染色体1q12的卫星III DNA进行FISH,证实了Southern杂交所获得的结果。重要的是,在所有5例被认为不涉及着丝粒区域的重排病例中,FISH显示这些事件并未破坏染色体的总体结构。这项研究突出了将这两种技术结合使用的潜力,以便更清楚地了解实体瘤中染色体的大规模和小规模改变情况。