Levsky Jeffrey M, Singer Robert H
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
J Cell Sci. 2003 Jul 15;116(Pt 14):2833-8. doi: 10.1242/jcs.00633.
Fluorescence in situ hybridization (FISH), the assay of choice for localization of specific nucleic acids sequences in native context, is a 20-year-old technology that has developed continuously. Over its maturation, various methodologies and modifications have been introduced to optimize the detection of DNA and RNA. The pervasiveness of this technique is largely because of its wide variety of applications and the relative ease of implementation and performance of in situ studies. Although the basic principles of FISH have remained unchanged, high-sensitivity detection, simultaneous assay of multiple species, and automated data collection and analysis have advanced the field significantly. The introduction of FISH surpassed previously available technology to become a foremost biological assay. Key methodological advances have allowed facile preparation of low-noise hybridization probes, and technological breakthroughs now permit multi-target visualization and quantitative analysis - both factors that have made FISH accessible to all and applicable to any investigation of nucleic acids. In the future, this technique is likely to have significant further impact on live-cell imaging and on medical diagnostics.
荧光原位杂交(FISH)是在自然环境中定位特定核酸序列的首选检测方法,这是一项有着20年历史且不断发展的技术。在其成熟过程中,人们引入了各种方法和改进措施来优化DNA和RNA的检测。这项技术的广泛应用很大程度上是因为其多种多样的应用以及原位研究相对容易实施和操作。尽管FISH的基本原理保持不变,但高灵敏度检测、多种物种的同时检测以及自动化数据收集和分析已使该领域取得了显著进展。FISH的引入超越了以前可用的技术,成为最重要的生物学检测方法。关键的方法学进展使得能够轻松制备低噪声杂交探针,而技术突破现在允许进行多靶点可视化和定量分析——这两个因素使得FISH为所有人所用,并适用于任何核酸研究。未来,这项技术可能会对活细胞成像和医学诊断产生重大的进一步影响。