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首页> 外文期刊>Nucleic acids research >The stability of duplexes involving AT and/or G4EtC base pairs is not dependent on their AT/G4EtC ratio content. Implication for DNA sequencing by hybridization
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The stability of duplexes involving AT and/or G4EtC base pairs is not dependent on their AT/G4EtC ratio content. Implication for DNA sequencing by hybridization

机译:涉及AT和/或G4EtC碱基对的双链体的稳定性不取决于其AT / G4EtC比含量。杂交对DNA测序的意义

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Sequencing by the recently reported hybridization technique requires the formation of DNA duplexes with similar stabilities. In this paper we describe a new strategy to obtain DNA duplexes with a thermal stability independent of their AT/GC ratio content. Melting data were acquired on 35 natural and 27 modified duplexes of a given length and of varying base compositions. Duplexes built with AT and/or G4EtC base pairs exhibit a thermal stability restrained to a lower range of temperature than that of the corresponding natural compounds (16 instead of 51°C). The 16°C difference in thermal stability observed between the least stable and the most stable duplex built with AT and/or G4EtC base pairs is mainly due to the sequence effect and not to their AT/G4EtC ratio content. Thus N-4-ethyl-2′-deoxycytidine (d4EtC) hybridizes specifically with natural deoxyguanosine leading to a G4EtC base pair whose stability is very close to that of the natural AT base pair. Oligonucleotide probes involving d4EtC can be easily prepared by chemical synthesis with phosphoramidite chemistry. Modified DNA targets were successfully amplified by random priming or PCR techniques using d4EtCTP, dATP, dGTP and dTTP in the presence of DNA polymerase. This new system might be very useful for DNA sequencing by hybridization.
机译:通过最近报道的杂交技术进行测序需要形成具有相似稳定性的DNA双链体。在本文中,我们描述了一种获得热稳定性独立于AT / GC比含量的DNA双链体的新策略。在给定长度和不同碱基组成的35个天然和27个修饰双链体上获得了熔解数据。用AT和/或G <4> Et 碱基对构建的双链体显示出比相应天然化合物低的温度范围(16而不是51°C)的热稳定性。用AT和/或G 4Et C碱基对构建的最不稳定和最稳定的双链体之间观察到的16°C热稳定性差异主要是由于序列效应而不是其AT / G 4Et C比含量。因此,N-4-乙基-2'-脱氧胞苷(d 4Et C)与天然脱氧鸟苷特异性杂交,形成G 4Et C碱基对,其稳定性非常接近于该碱基对。自然AT碱基对。含有d 4Et C的寡核苷酸探针可以很容易地通过亚磷酰胺化学合成来制备。在DNA聚合酶存在下,使用d 4Et CTP,dATP,dGTP和dTTP通过随机引物或PCR技术成功扩增了修饰的DNA靶标。这个新系统可能对通过杂交进行DNA测序非常有用。

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