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一段不会导致DNA弯曲的腺嘌呤序列的结构细节。

Structural details of an adenine tract that does not cause DNA to bend.

作者信息

Burkhoff A M, Tullius T D

机构信息

Department of Biology, Johns Hopkins University, Baltimore, Maryland 21218.

出版信息

Nature. 1988 Feb 4;331(6155):455-7. doi: 10.1038/331455a0.

Abstract

Runs of adenines (adenine tracts) have been implicated as the main determinant of sequence-directed DNA bending. The most widely used experimental test for bending relies on the observation that bent DNA migrates more slowly than straight DNA on a polyacrylamide electrophoresis gel. It was shown recently that the polymer (GTTTTAAAAC)n runs with normal mobility on a gel, whereas (GAAAATTTTC)n runs more slowly and thus appears to be strongly bent. The observation that these similar sequences, which differ only in the order of the adenine and thymine tracts, adopt such different shapes offers a stringent test of theories to explain DNA bending. Although the wedge model for DNA bending has recently been elaborated to explain the gel mobilities of these molecules, we wished to determine experimentally the structural basis for the difference in bending. We report here measurements of the frequency of cleavage by the hydroxyl radical at each nucleotide of cloned versions of the two polymers (see Fig. 1). We show that the TTTTAAAA sequence does not display the cleavage pattern that is associated with bent DNA, whereas the AAAATTTT sequence does. The observed sequence dependence of the cleavage pattern of an adenine tract is at odds with current models for DNA bending, which assume that adenine tracts always adopt the same conformation.

摘要

腺嘌呤串联序列(腺嘌呤片段)被认为是序列导向的DNA弯曲的主要决定因素。用于检测弯曲的最广泛使用的实验方法依赖于这样的观察结果:在聚丙烯酰胺电泳凝胶上,弯曲的DNA比直的DNA迁移得更慢。最近有研究表明,聚合物(GTTTTAAAAC)n在凝胶上以正常迁移率移动,而(GAAAATTTTC)n迁移得更慢,因此似乎有强烈的弯曲。这些仅在腺嘌呤和胸腺嘧啶片段顺序上不同的相似序列呈现出如此不同形状的观察结果,为解释DNA弯曲的理论提供了严格的检验。尽管最近已经详细阐述了DNA弯曲的楔形模型来解释这些分子的凝胶迁移率,但我们希望通过实验确定弯曲差异的结构基础。我们在此报告了对两种聚合物克隆版本中每个核苷酸处羟基自由基切割频率的测量(见图1)。我们发现,TTTTAAAA序列没有显示出与弯曲DNA相关的切割模式,而AAAATTTT序列则有。观察到的腺嘌呤片段切割模式的序列依赖性与当前的DNA弯曲模型不一致,当前模型假定腺嘌呤片段总是采用相同的构象。

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