首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Sequence Context Effect on Strand Slippage in Natural DNA Primer-Templates
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Sequence Context Effect on Strand Slippage in Natural DNA Primer-Templates

机译:序列背景对天然DNA引物模板中链滑动的影响

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摘要

Strand slippage has been found to occur in primer-templates containing a templating thymine, cytosine, and guanine, leading to the formation of misaligned structures with a single-nucleotide bulge. If remained in the active site of low-fidelity polymerases during DNA replication, these misaligned structures can ultimately bring about deletion mutations. In this study, we performed NMR investigations on primer-template models containing a templating adenine. Similar to our previous results on guanine, adenine templates are also less prone to strand slippage than pyrimidine templates. Misalignment occurs only in primer-templates that form a terminal C·G or G·C base pair. Together with our previous findings on thymine, cytosine, and guanine templates, the present study reveals strand slippage can occur in any kind of natural templating bases during DNA replication, providing insights into the origin of mutation hotspots in natural DNA sequences. In addition to the type of incoming base upon misincorporation, the propensity of strand slippage in primer-templates depends also on the type of templating base, its upstream and downstream bases.
机译:已经发现在包含模板胸腺嘧啶,胞嘧啶和鸟嘌呤的引物模板中发生链滑动,导致形成具有单核苷酸凸起的错位结构。如果在DNA复制过程中保留在低保真聚合酶的活性位点,这些错位的结构最终会导致缺失突变。在这项研究中,我们对包含模板腺嘌呤的引物-模板模型进行了NMR研究。与我们以前关于鸟嘌呤的结果相似,腺嘌呤模板也比嘧啶模板不容易发生链滑动。错位仅在形成末端C·G或G·C碱基对的引物模板中发生。结合我们先前在胸腺嘧啶,胞嘧啶和鸟嘌呤模板上的发现,本研究表明链滑移可能发生在DNA复制过程中的任何类型的天然模板碱基中,从而洞察了天然DNA序列中突变热点的起源。除了因掺入错误而引入的碱基的类型外,引物模板中链滑动的倾向还取决于模板碱基的类型,其上游和下游碱基。

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