From the Lineberger Comprehensive Cancer Center, University of North Carolina-Chapel Hill, Chapel Hill, North Carolina 27599.
the Department of Cancer Biology and Genetics, Ohio State University Wexner Medical Center, Columbus, Ohio 43210.
J Biol Chem. 2018 Jun 15;293(24):9473-9485. doi: 10.1074/jbc.RA118.002158. Epub 2018 Apr 19.
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 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') , 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.
长链单链 DNA(ssDNA)的构象是理解复制叉、R 环和其他在 DNA 代谢过程中产生的结构的核心关注点。如果 ssDNA 由短核苷酸重复组成,情况尤其如此。这些研究受到缺乏大于约 150 个核苷酸的定义明确的底物和缺乏高分辨率生物物理方法的阻碍。在这里,我们描述了由哺乳动物端粒重复(5'-TTAGGG-3')组成的非常长的 ssDNA 的产生,以及通过 EM 和单分子磁镊(smMT)对其结构的检测。这种重复特别有趣,因为它包含一个连续三个鸟嘌呤残基的序列,这些残基能够形成 ssDNA 中的 G 四联体。荧光染料排除测定证实了这种 G 链 ssDNA 形成了普遍存在的 G-四联体折叠。EM 揭示了浓缩 DNA 约 12 倍的厚珠状纤维。珠状结构的直径为 5nm 和 8nm,由细纤维连接。G 链 ssDNA 显示出对 smMT 力延伸的初始稳定性,最终以倍数为 28nm 的步释放,在 6 到 12pN 之间的力下,这远低于解开 G-四联体所需的 >20pN。大多数 smMT 步骤与 EM 中观察到的珠状结构的破坏一致。RAD51 的结合显著改变了 G 链 ssDNA 的力延伸特性,表明存在一种随机的 G-四联体依赖的凝聚模型,对此进行了讨论。