Genome. 1994 Dec;37(6):1062-5. doi: 10.1139/g94-151.
We describe a direct and sensitive fluorescence in situ hybridization protocol for plant chromosomes. We labelled 45S rDNA with fluorescein-12-dUTP and hybridized to somatic chromosomes of four tomato genotypes. This technique does not require posthybridization immunocytochemical amplifications. The improved signal sensitivity with this technique allowed identification of new rDNA loci on three pairs of chromosomes, in addition to the previously known locus on chromosome 2. We discuss favorable features of direct fluorescence in situ hybridization for chromosomes fixed on a slide and chromosomes or cells in suspension.
我们描述了一种用于植物染色体的直接且灵敏的荧光原位杂交(FISH)方案。我们用荧光素-12-dUTP 标记 45S rDNA,并将其与四个番茄基因型的体细胞染色体杂交。该技术不需要杂交后的免疫细胞化学扩增。与该技术相比,这种方法提高了信号灵敏度,除了先前在第 2 号染色体上已知的位点外,还可以鉴定出另外三对染色体上的新 rDNA 位点。我们讨论了将固定在载玻片上的染色体以及悬浮的染色体或细胞进行直接荧光原位杂交的有利特征。