Tsvetkov Vladimir B
Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine, Moscow 119435, Russia.
Center for Mathematical Modeling in Drug Development, I.M. Sechenov First Moscow State Medical University, Trubetskaya Str. 8-2, Moscow 119991, Russia.
Int J Mol Sci. 2025 Jun 21;26(13):5979. doi: 10.3390/ijms26135979.
Tetrahelical DNA structures, such as G-quadruplexes (G4s) or i-motifs (iMs), are adopted by sequences comprising several G/C tracts, exist in equilibria with respective duplexes, and may contribute to genomic instability upon helicase deficiency. To understand genomic rearrangements resulting from the juxtaposition of G/C-rich DNA duplexes, models of possible intermediate structures are needed. In this study, a general strategy for creating and verifying in silico 3D models of tetrahelical DNA was proposed. This strategy was used to investigate contacts of two or more duplexes with n G/C tracts ( = 2-6) separated by T/A nucleotides. The revealed viable structures of DNA-DNA contacts include stacks of right-handed and left-handed G-quadruplexes (G4s), Holliday structure-resembling assemblies with the G4 and iM opposite each other on the borders of the central "hole", etc. Based on molecular dynamic simulations, the most probable variants were determined by estimating the contributions to the free energy. The results may be used to clarify the mechanisms of strand exchange and other rearrangements upon DNA breaks near prolonged G/C-rich sites in living systems. Additionally, they provide a balanced view on the polymorphic programmed DNA assemblies in artificial systems.
四螺旋DNA结构,如G-四链体(G4s)或i-基序(iMs),由包含几个G/C片段的序列形成,与各自的双链体处于平衡状态,并且在解旋酶缺乏时可能导致基因组不稳定。为了理解富含G/C的DNA双链体并置导致的基因组重排,需要可能的中间结构模型。在本研究中,提出了一种创建和验证四螺旋DNA的计算机三维模型的通用策略。该策略用于研究两个或多个由T/A核苷酸隔开的具有n个G/C片段(n = 2-6)的双链体之间的接触。所揭示的DNA-DNA接触的可行结构包括右手和左手G-四链体(G4s)的堆叠、在中央“孔”的边界上G4和iM彼此相对的类霍利迪结构组装体等。基于分子动力学模拟,通过估计对自由能的贡献来确定最可能的变体。这些结果可用于阐明生物系统中富含G/C的延长位点附近DNA断裂时链交换和其他重排的机制。此外,它们为人工系统中多态性程序化DNA组装提供了一个平衡的观点。