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揭示 DNA i 型发夹结构稳定性的 4n-1 规则:碱基对与环长。

Unraveling the 4n - 1 rule for DNA i-motif stability: base pairs vs. loop lengths.

机构信息

Department of Chemistry, 315 S. 1400 East. and University of Utah, Salt Lake City, UT 84112-0850, USA.

出版信息

Org Biomol Chem. 2018 Jun 20;16(24):4537-4546. doi: 10.1039/c8ob01198b.

DOI:10.1039/c8ob01198b
PMID:29873385
Abstract

Previously our laboratory identified that poly-2'-deoxycytidine (dCn) strands of DNA with lengths greater than 12 nucleotides could adopt i-motif folds, while the pH-dependent stabilities follow a 4n - 1 repeat pattern with respect to chain length (J. Am. Chem. Soc., 2017, 139, 4682-4689). Herein, model i-motif folds in which loop configurations were forced by judiciously mutating dC to non-dC nucleotides allowed a structural model to be proposed to address this phenomenon. The model was developed by systematically studying two i-motifs with either an even or odd number of d(C·C)+ hemiprotonated base pairs in the core. First, a trend in the pH-dependent stability vs. loop nucleotide identity was observed: dC > dT ∼ dU ≫ dA ∼ dG. Next, loops comprised of dT nucleotides in the two different core base pair configurations were studied while systematically changing the loop lengths. We found that an i-motif with an even number of base pairs in the core with a single nucleotide in each of the three loops was the most stable, as well as an i-motif with an odd number of core base pairs having one nucleotide in the two exterior loops and three nucleotides in the central loop. A systematic increase in the central loop from 1-4 nucleotides for an odd number of base pairs in the i-motif core reproduced the 4n - 1 repeat pattern observed in the poly-dCn strands. Additional loop configurations were studied to further support the model. The results are discussed with respect to their biological relevance.

摘要

此前,我们实验室已经确定,长度大于 12 个核苷酸的聚 2'-脱氧胞苷(dCn)链可以形成 i- 发夹结构,而 pH 依赖性稳定性则遵循链长的 4n-1 重复模式(J. Am. Chem. Soc.,2017,139,4682-4689)。在此,通过巧妙地将 dC 突变为非 dC 核苷酸来强制形成环构象的模型 i- 发夹结构,允许提出一个结构模型来解决这一现象。该模型是通过系统研究两个 i- 发夹结构来建立的,这两个 i- 发夹结构的核心中分别具有偶数或奇数个 d(C·C)+半质子化碱基对。首先,观察到 pH 依赖性稳定性与环核苷酸身份之间的趋势:dC>dT∼dU≫dA∼dG。接下来,研究了在两种不同核心碱基对构象中包含 dT 核苷酸的环,同时系统地改变环的长度。我们发现,核心中具有偶数个碱基对且每个环中各有一个核苷酸的 i- 发夹结构最稳定,以及核心中具有奇数个碱基对且两个外部环中各有一个核苷酸且中央环中有三个核苷酸的 i- 发夹结构最稳定。对于核心中具有奇数个碱基对的 i- 发夹结构,中央环从 1 到 4 个核苷酸的系统增加再现了在多聚 dCn 链中观察到的 4n-1 重复模式。进一步研究了其他环构象以进一步支持该模型。讨论了这些结果及其生物学相关性。

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