Division of Chemistry, Department of Medical Sciences, Faculty of Medicine, University of Miyazaki, Japan.
Research Center for Advanced Science and Technology, The University of Tokyo, Japan.
Sci Rep. 2016 Sep 13;6:33217. doi: 10.1038/srep33217.
Chromosome visualization is essential for chromosome analysis and genetic diagnostics. Here, we developed a click chemistry approach for multicolor imaging of chromosomal DNA instead of the traditional dye method. We first demonstrated that the commercially available reagents allow for the multicolor staining of chromosomes. We then prepared two pro-fluorophore moieties that served as light-up reporters to stain chromosomal DNA based on click reaction and visualized the clear chromosomes in multicolor. We applied this strategy in fluorescence in situ hybridization (FISH) and identified, with high sensitivity and specificity, telomere DNA at the end of the chromosome. We further extended this approach to observe several basic stages of cell division. We found that the click reaction enables direct visualization of the chromosome behavior in cell division. These results suggest that the technique can be broadly used for imaging chromosomes and may serve as a new approach for chromosome analysis and genetic diagnostics.
染色体显影对于染色体分析和遗传诊断至关重要。在这里,我们开发了一种点击化学方法,用于对染色体 DNA 进行多色成像,而不是传统的染色方法。我们首先证明,市售的试剂允许对染色体进行多色染色。然后,我们制备了两个前荧光团部分,作为点亮报告子,基于点击反应对染色体 DNA 进行染色,并以多色观察到清晰的染色体。我们将这种策略应用于荧光原位杂交 (FISH) 中,并以高灵敏度和特异性识别染色体末端的端粒 DNA。我们进一步扩展了这种方法来观察细胞分裂的几个基本阶段。我们发现,点击反应能够直接观察细胞分裂过程中的染色体行为。这些结果表明,该技术可广泛用于染色体成像,并可能成为染色体分析和遗传诊断的新方法。