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一种通过多重荧光原位杂交(M-FISH)快速准确识别染色体重排的优化全自动系统。

An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH).

作者信息

Eils R, Uhrig S, Saracoglu K, Sätzler K, Bolzer A, Petersen I, Chassery J, Ganser M, Speicher M R

机构信息

Interdisciplinary Center of Scientific Computing, University of Heidelberg, Heidelberg (Germany).

出版信息

Cytogenet Cell Genet. 1998;82(3-4):160-71. doi: 10.1159/000015092.

DOI:10.1159/000015092
PMID:9858809
Abstract

Multiplex-FISH (M-FISH) is a recently developed technique by which each of the two dozen human chromosomes-the 22 autosomes and the X and Y sex chromosomes-can be stained or "painted" with uniquely distinctive colors. Using a combinatorial labeling technique and a specially designed filter set, each DNA probe can be identified by its unique spectral signature. Here we present several significant optimizations of the M-FISH technology. First, a new strategy for labeling the probes is described which allows for easy and fast production of the complex M-FISH probe mix. Second, a newly developed, completely motorized microscope equipped with an eight-position filter wheel and a new generation of filter sets is presented that allows fully automatic imaging of a complete metaphase spread within seconds. Third, to determine the characteristic spectral signatures for all different combinations of fluorochromes, we developed a novel multichannel image analysis method. The spectral analysis is solely guided by the image information itself and does not require any user interaction. A complete analysis of a metaphase spread can be accomplished in less than 3 min. Sophisticated built-in quality controls were developed, and the value of visual inspection of M-FISH images as a simple means of controlling the computer-generated chromosome classification are illustrated. In addition, we discuss advantages of adding new fluorochromes to the traditionally used five fluorochromes.

摘要

多重荧光原位杂交(M-FISH)是一项最近开发的技术,通过该技术,人类的24条染色体(22条常染色体以及X和Y性染色体)中的每一条都可以用独特的颜色进行染色或“描绘”。使用组合标记技术和专门设计的滤光片组,每个DNA探针都可以通过其独特的光谱特征来识别。在此,我们展示了M-FISH技术的几个重要优化。首先,描述了一种标记探针的新策略,该策略允许轻松快速地制备复杂的M-FISH探针混合物。其次,展示了一种新开发的、完全自动化的显微镜,其配备了八位置滤光轮和新一代滤光片组,能够在几秒钟内对完整中期染色体进行全自动成像。第三,为了确定所有不同荧光染料组合的特征光谱特征,我们开发了一种新颖的多通道图像分析方法。光谱分析完全由图像信息本身引导,不需要任何用户交互。对中期染色体的完整分析可以在不到3分钟内完成。我们开发了复杂的内置质量控制,并说明了对M-FISH图像进行目视检查作为控制计算机生成的染色体分类的一种简单方法的价值。此外,我们还讨论了在传统使用的五种荧光染料中添加新荧光染料的优点。

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An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH).一种通过多重荧光原位杂交(M-FISH)快速准确识别染色体重排的优化全自动系统。
Cytogenet Cell Genet. 1998;82(3-4):160-71. doi: 10.1159/000015092.
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