首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Long repeating (TTAGGG)n single-stranded DNA self-condenses into compact beaded filaments stabilized by G-quadruplex formation
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Long repeating (TTAGGG)n single-stranded DNA self-condenses into compact beaded filaments stabilized by G-quadruplex formation

机译:长重复(TTAGGG)n单链DNA自凝结成紧密的串珠丝并通过G-四链体形成而稳定

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摘要

Conformations adopted by long stretches of single-stranded DNA (ssDNA) are of central interest in understanding the architecture of replication forks, R loops, and other structures generated during DNA metabolism in vivo. This is particularly so if the ssDNA consists of short nucleotide repeats. Such studies have been hampered by the lack of defined substrates greater than ∼150 nt and the absence of high-resolution biophysical approaches. Here we describe the generation of very long ssDNA consisting of the mammalian telomeric repeat (5′-TTAGGG-3′)n, as well as the interrogation of its structure by EM and single-molecule magnetic tweezers (smMT). This repeat is of particular interest because it contains a run of three contiguous guanine residues capable of forming G quartets as ssDNA. Fluorescent-dye exclusion assays confirmed that this G-strand ssDNA forms ubiquitous G-quadruplex folds. EM revealed thick bead-like filaments that condensed the DNA ∼12-fold. The bead-like structures were 5 and 8 nm in diameter and linked by thin filaments. The G-strand ssDNA displayed initial stability to smMT force extension that ultimately released in steps that were multiples ∼28 nm at forces between 6 and 12 pN, well below the >20 pN required to unravel G-quadruplexes. Most smMT steps were consistent with the disruption of the beads seen by EM. Binding by RAD51 distinctively altered the force extension properties of the G-strand ssDNA, suggesting a stochastic G-quadruplex-dependent condensation model that is discussed.
机译:长链单链DNA(ssDNA)所采用的构象是了解复制叉,R环和体内DNA代谢过程中产生的其他结构的结构的主要兴趣。如果ssDNA由短核苷酸重复组成,则尤其如此。由于缺乏确定的大于150nt的底物以及缺乏高分辨率的生物物理方法,这些研究受到了阻碍。在这里,我们描述了由哺乳动物端粒重复序列(5'-TTAGGG-3')n组成的非常长的ssDNA的生成,以及由EM和单分子磁性镊子(smMT)对其结构的询问。该重复序列是特别令人感兴趣的,因为它包含三个能够形成G四重奏作为ssDNA的连续的鸟嘌呤残基。荧光染料排除试验证实,该G链ssDNA形成遍在的G-四链体折叠。 EM显示出粗大的珠子状细丝,将DNA浓缩了约12倍。珠状结构的直径分别为5和8 nm,并通过细丝连接。 G链ssDNA对smMT力延伸显示出初始稳定性,最终在6到12 pN之间的力下以〜28 nm的倍数逐步释放,远低于解开G-四链体所需的> 20 pN。大多数smMT步骤与EM观察到的珠子破坏一致。通过RAD51的结合显着改变了G链ssDNA的力延伸特性,表明了讨论的随机G-四链体依赖性缩合模型。

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