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用于可视化活细胞中重复DNA序列的聚酰胺荧光探针。

Polyamide fluorescent probes for visualization of repeated DNA sequences in living cells.

作者信息

Nozeret Karine, Loll François, Escudé Christophe, Boutorine Alexandre S

机构信息

Structure and Instability of Genomes, Sorbonne Universités, Muséum national d'Histoire naturelle, INSERM U 1154, CNRS UMR 7196, 57 rue Cuvier, C.P. 26, 75231 Paris Cedex 05 (France).

出版信息

Chembiochem. 2015 Mar 2;16(4):549-54. doi: 10.1002/cbic.201402676. Epub 2015 Jan 30.

DOI:10.1002/cbic.201402676
PMID:25639955
Abstract

DNA imaging in living cells usually requires transgenic approaches that modify the genome. Synthetic pyrrole-imidazole polyamides that bind specifically to the minor groove of double-stranded DNA (dsDNA) represent an attractive approach for in-cell imaging that does not necessitate changes to the genome. Nine hairpin polyamides that target mouse major satellite DNA were synthesized. Their interactions with synthetic target dsDNA fragments were studied by thermal denaturation, gel-shift electrophoresis, circular dichroism, and fluorescence spectroscopy. The polyamides had different affinities for the target DNA, and fluorescent labeling of the polyamides affected their affinity for their targets. We validated the specificity of the probes in fixed cells and provide evidence that two of the probes detect target sequences in mouse living cell lines. This study demonstrates for the first time that synthetic compounds can be used for the visualization of the nuclear substructures formed by repeated DNA sequences in living cells.

摘要

活细胞中的DNA成像通常需要修饰基因组的转基因方法。特异性结合双链DNA(dsDNA)小沟的合成吡咯-咪唑聚酰胺代表了一种用于细胞内成像的有吸引力的方法,这种方法无需改变基因组。合成了九种靶向小鼠主要卫星DNA的发夹聚酰胺。通过热变性、凝胶迁移电泳、圆二色性和荧光光谱研究了它们与合成靶标dsDNA片段的相互作用。这些聚酰胺对靶标DNA具有不同的亲和力,并且聚酰胺的荧光标记影响它们对靶标的亲和力。我们在固定细胞中验证了探针的特异性,并提供证据表明其中两种探针可检测小鼠活细胞系中的靶标序列。这项研究首次证明合成化合物可用于可视化活细胞中由重复DNA序列形成的核亚结构。

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