Kearney L
Section of Haemato-Oncology, Institute of Cancer Research, London, UK.
Cytogenet Genome Res. 2006;114(3-4):189-98. doi: 10.1159/000094202.
Multiplex FISH (M-FISH) represents one of the most significant developments in molecular cytogenetics of the past decade. Originally designed to generate 24 colour karyotyping, the technique has spawned many variations and an equally diverse range of applications. In tumour and leukaemia cytogenetics, the two groups that have been targeted represent both ends of the cytogenetic spectrum: those with an apparently normal karyotype (suspected of harbouring small rearrangements not detectable by conventional cytogenetics) and those with a complex aberrant karyotype (which are difficult to karyotype accurately due to the sheer number of aberrations). In research, mouse M-FISH provides a powerful tool to characterize mouse models of a disease. In addition, the ability to accurately karyotype single metaphases without selection makes M-FISH the perfect tool in chromosome breakage studies and for characterizing clonal evolution of tumours. Finally, M-FISH has emerged as the perfect partner for the developing genomic microarray (array CGH) technologies, providing a powerful approach to gene discovery.
多重荧光原位杂交(M-FISH)是过去十年分子细胞遗传学领域最重要的进展之一。该技术最初旨在生成24色核型分析,现已衍生出许多变体和同样多样的应用。在肿瘤和白血病细胞遗传学中,被靶向的两组代表了细胞遗传学谱系的两端:一组核型明显正常(怀疑存在常规细胞遗传学无法检测到的小重排),另一组核型复杂异常(由于畸变数量众多,难以准确进行核型分析)。在研究中,小鼠M-FISH为表征疾病的小鼠模型提供了强大工具。此外,无需选择就能准确分析单个中期细胞的核型,这使得M-FISH成为染色体断裂研究以及表征肿瘤克隆进化的理想工具。最后,M-FISH已成为新兴的基因组微阵列(阵列比较基因组杂交)技术的完美搭档,为基因发现提供了强大方法。