Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991, Moscow, Russia.
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991, Moscow, Russia.
Biochimie. 2019 May;160:122-128. doi: 10.1016/j.biochi.2019.02.013. Epub 2019 Mar 3.
Conformation of the telomeric DNA fragment dG(TTAG) depends on multiple factors including solution conditions, length, and the nucleotide sequence of the flanking regions. In potassium solution, this sequence tends to adopt hybrid (3 + 1) G-quadruplex (G4) Form 1 or Form 2 conformation contingent on the flanking nucleotides. Theoretically, other (3 + 1) G4 folds (beyond Forms 1 and 2) are not sterically forbidden, but are presumably energetically disfavored. We report here on the effect of substituting the TTA loop with a single T nucleotide for one, two, or three loops of telomeric DNA that allowed us to expand the conformational diversity of the G4 DNA. Circular dichroism, gel migration, and chemical probing with DMS and ZnP1 (a porphyrin derivative sensitive to G4 conformation) were applied to monitor conformations that occurred upon shortening each loop to a single nucleotide. We found that all oligonucleotide models formed an intramolecular quadruplex structure and that shortening the loops led to the prevalence of G4 with quartets of the same polarity. Despite similar CD signatures, each modified sequence had one of three specific patterns of light-induced oxidation with ZnP1. According to the predominant modification pattern, folding of each sequence could be assigned to one of three major G4 conformations: parallel and two different (3 + 1) G4 folds. We here provide novel experimental evidence of the propensity for modified telomeric sequences to form a (3 + 1) G4 conformer containing one lateral and two propeller loops.
端粒 DNA 片段 dG(TTAG)的构象取决于多种因素,包括溶液条件、长度和侧翼区域的核苷酸序列。在钾溶液中,该序列倾向于采用杂交(3+1)G-四链体(G4)形式 1 或形式 2,这取决于侧翼核苷酸。从理论上讲,其他(3+1)G4 折叠(超出形式 1 和 2)在空间上不是禁止的,但可能在能量上是不利的。我们在这里报告了用单个 T 核苷酸替代 TTA 环的效果,对于端粒 DNA 的一个、两个或三个环进行了取代,这使我们能够扩展 G4 DNA 的构象多样性。圆二色性、凝胶迁移和用 DMS 和 ZnP1(一种对 G4 构象敏感的卟啉衍生物)进行化学探测被应用于监测每个环缩短到单个核苷酸时发生的构象。我们发现所有寡核苷酸模型都形成了分子内四链体结构,并且缩短环导致具有相同极性四联体的 G4 占优势。尽管 CD 特征相似,但每种修饰序列都具有 ZnP1 光诱导氧化的三种特定模式之一。根据主要修饰模式,每个序列的折叠可以分配到三种主要 G4 构象之一:平行和两种不同的(3+1)G4 折叠。我们在这里提供了修饰端粒序列形成含有一个侧向和两个推进器环的(3+1)G4 构象体的倾向的新的实验证据。