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Design of modified oligodeoxyribonucleotide probes to detect telomere repeat sequences in FISH assays.

机译:设计修饰的寡脱氧核糖核苷酸探针以检测FISH分析中的端粒重复序列。

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摘要

A series of dye-labeled oligonucleotide probes containing base and sugar modifications were tested for the ability to detect telomeric repeat sequences in FISH assays. These modified oligonucleotides, all 18 nt in length, were complementary to either the cytidine-rich (C(3)TA(2))(n)or guanosine-rich (T(2)AG(3))(n)telomere target sequences. Oligonucleotides were modified to either increase target affinity by enhancing duplex stability [2'-OMe ribose sugars and 5-(1-propynyl)pyrimidine residues] or inhibit the formation of inter- or intramolecular structures (7-deazaguanosine and 6-thioguanosine residues), which might interfere with binding to the target. Several dye-labeled oligonucleotide probes were found that could effectively stain the telomeric repeat sequences of either cytidine- or guanosine-rich strands in a specific manner. Such probes could be used as an alternative to peptide nucleic acids for investigating the dynamics of telomere length and maintenance. In principle, these relatively inexpensive and readily synthesized modified oligonucleotides could be used for other FISH-related assays.
机译:测试了一系列含有碱基和糖修饰基团的染料标记寡核苷酸探针在FISH分析中检测端粒重复序列的能力。这些修饰的寡核苷酸,全长均为18 nt,与富含胞苷的(C(3)TA(2))(n)或富含鸟苷的(T(2)AG(3))(n)端粒靶标互补序列。修饰寡核苷酸以通过增强双链体稳定性[2'-OMe核糖和5-(1-丙炔基)嘧啶残基]增加靶标亲和力,或抑制分子间或分子内结构的形成(7-脱氮鸟苷和6-硫鸟苷残基) ,这可能会干扰与目标的绑定。发现了几种染料标记的寡核苷酸探针,它们可以以特定方式有效地染色富含胞苷或鸟苷的链的端粒重复序列。这样的探针可以用作肽核酸的替代物,用于研究端粒长度和维持的动力学。原则上,这些相对便宜且易于合成的修饰寡核苷酸可用于其他FISH相关测定。

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