Spivak Graciela
Department of Biology, Stanford University, 385 Serra Mall, Stanford, CA 94395-5020, USA
Mutagenesis. 2015 Jan;30(1):5-9. doi: 10.1093/mutage/geu036.
The comet assay combined with fluorescence in-situ hybridisation (FISH) is a powerful technique for comparative analyses of damage induction and repair in genomes and in specific DNA sequences within single cells. Recent advances in the methodology of comet-FISH will be considered here, with particular attention to the design and generation of fluorescent probes. In general, all the approaches must fulfil a few basic requirements: the probes should be no longer than ~300 nucleotides in length (single or double stranded) to be able to penetrate the gel in which the target genomic DNA is embedded, they should be sequence-specific, and their signal should be detectable and distinct from the background fluorescence and the dye used to stain the DNA.
彗星试验结合荧光原位杂交(FISH)是一种强大的技术,可用于比较分析单个细胞内基因组和特定DNA序列中的损伤诱导和修复情况。本文将探讨彗星-FISH方法的最新进展,尤其关注荧光探针的设计和生成。一般来说,所有方法都必须满足一些基本要求:探针长度(单链或双链)应不超过约300个核苷酸,以便能够穿透嵌入目标基因组DNA的凝胶;它们应具有序列特异性,并且其信号应可检测,且与背景荧光和用于染色DNA的染料不同。