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A序列中DNA弯曲时A链与T链小沟相互作用的直接比较。

Direct comparison of A- and T-strand minor groove interactions in DNA curvature at A tracts.

作者信息

Maki Angèle S, Kim TaeWoo, Kool Eric T

机构信息

Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA.

出版信息

Biochemistry. 2004 Feb 3;43(4):1102-10. doi: 10.1021/bi035340m.

Abstract

To investigate the relative contributions of minor-groove electrostatic interactions in the mechanism of A-tract DNA curvature, we carried out experiments with modified DNA bases in both strands of the tract. We employed 3-deazaadenine nucleoside (D), which lacks the adenine N3 nitrogen in the minor groove and thus cannot act as an electron donor, as well as difluorotoluene (F), a nonpolar thymine mimic. The effects of these analogues in A-tract curvature were quantified using ligation ladder gel mobility methods developed by Crothers and by Maher. Through single substitutions of D in A(5) tracts, we found that this analogue results in decreased curvature only when situated toward the 3' end of the tract. This is distinct from the behavior in the T-rich strand where F substitution causes the greatest reductions in curvature toward the 5' end. To test for cooperative pairwise effects, we also studied 10 different D + F double substitutions and found evidence supporting a number of localized cooperative electrostatic interactions but not between the two most sensitive sites in the opposite strands. These results suggest that there are two discrete locations in the A-tract minor groove where electrostatic interactions are important in causing curvature: one near the 5' end of the T-rich strand, and one near the 3' end of the A-rich strand. The results are consistent with an important role of localized cations in the minor groove. Possible effects of groove solvation and stacking at the A-tract junction are also discussed.

摘要

为了研究小沟静电相互作用在A-序列DNA弯曲机制中的相对贡献,我们对该序列两条链中的DNA碱基进行了修饰实验。我们使用了3-脱氮腺嘌呤核苷(D),它在小沟中缺少腺嘌呤的N3氮,因此不能作为电子供体,以及二氟甲苯(F),一种非极性的胸腺嘧啶类似物。使用由克罗瑟斯和马赫开发的连接梯凝胶迁移方法对这些类似物在A-序列弯曲中的作用进行了量化。通过在A(5)序列中单个替换D,我们发现只有当该类似物位于序列的3'端时,才会导致弯曲度降低。这与富含胸腺嘧啶的链中的行为不同,在该链中F替换导致朝向5'端的弯曲度最大程度降低。为了测试协同成对效应,我们还研究了10种不同的D + F双替换,并发现有证据支持一些局部协同静电相互作用,但不是在相反链中两个最敏感位点之间。这些结果表明,在A-序列小沟中有两个离散位置,静电相互作用在导致弯曲方面很重要:一个靠近富含胸腺嘧啶链的5'端,另一个靠近富含腺嘌呤链的3'端。结果与小沟中局部阳离子的重要作用一致。还讨论了A-序列连接处小沟溶剂化和堆积的可能影响。

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