Liehr T, Starke H, Weise A, Lehrer H, Claussen U
Institute of Human Genetics and Anthropology, Jena, Germany.
Histol Histopathol. 2004 Jan;19(1):229-37. doi: 10.14670/HH-19.229.
Multicolor fluorescence in situ hybridization (FISH) assays are nowadays indispensable for a precise description of complex chromosomal rearrangements. Routine application of such techniques on human chromosomes started in 1996 with the simultaneous use of all 24 human whole chromosome painting probes in multiplex-FISH (M-FISH) and spectral karyotyping (SKY). Since then different approaches for chromosomal differentiation based on multicolor-FISH (mFISH) assays have been described. Predominantly, they have been established to characterize marker chromosomes identified in conventional banding analysis. Their characterization is of high clinical impact and is the requisite condition for further molecular investigations aimed at the identification of disease-related genes. Here we present a review on the available mFISH methods including their advantages, limitations and possible applications.
如今,多色荧光原位杂交(FISH)分析对于精确描述复杂的染色体重排不可或缺。1996年开始将此类技术常规应用于人类染色体,当时在多重FISH(M-FISH)和光谱核型分析(SKY)中同时使用了所有24种人类全染色体涂染探针。从那时起,已经描述了基于多色FISH(mFISH)分析的不同染色体分化方法。主要是,这些方法已被确立用于鉴定常规显带分析中识别出的标记染色体。它们的鉴定具有很高的临床意义,并且是旨在鉴定疾病相关基因的进一步分子研究的必要条件。在此,我们对现有的mFISH方法进行综述,包括其优点、局限性和可能的应用。