The "very moment" when UDG recognizes aflipped-out uracil base in dsDNA

Vinnarasi Saravanan, Nessim Raouraoua, Guillaume Brysbaert, Stefano Giordano, Marc F Lensink, Fabrizio Cleri, Ralf Blossey
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Abstract

Uracil-DNA glycosylase (UDG) is the first enzyme in the base-excision repair (BER) pathway, acting on uracil bases in DNA. How UDG finds its targets has not been conclusively resolved yet. Based on available structural and other experimental evidence, two possible pathways are under discussion. In one, the action of UDG on the DNA bases is believed to follow a "pinch-push-pull" model, in which UDG generates the base-flip in an active manner. A second scenario is based on the exploitation of bases flipping out thermally from the DNA. Recent molecular dynamics (MD) studies of DNA in trinucleosome arrays have shown that base-flipping can be readily induced by the action of mechanical forces on DNA alone. This alternative mechanism could possibly enhance the probability for the second scnenario of UDG- uracil interaction via the formation of a recognition complex of UDG with flipped-out base. In this work we describe DNA structures with flipped-out uracil bases generated by MD simulations which we then subject to docking simulations with the UDG enzyme. Our results for the UDG-uracil recognition complex support the view that base-flipping induced by DNA mechanics can be a relevant mechanism of uracil base recognition by the UDG glycosylase in chromatin.
UDG 识别 dsDNA 中翻转的尿嘧啶碱基的 "非常时刻"
尿嘧啶-DNA 糖基化酶(UDG)是碱基切除修复(BER)途径中的第一种酶,作用于 DNA 中的尿嘧啶碱基。UDG 如何找到它的目标尚未得到最终解决。根据现有的结构和其他实验证据,目前正在讨论两种可能的途径。其一,UDG 对 DNA 碱基的作用被认为遵循 "捏-推-拉 "模式,即 UDG 以主动方式产生碱基翻转。第二种情况是利用碱基在 DNA 中的热翻转。最近对三核体阵列中 DNA 的分子动力学(MD)研究表明,仅通过 DNA 上的机械力就能轻易诱导碱基翻转。这种替代机制有可能通过 UDG 与翻转碱基形成识别复合物,提高 UDG 与尿嘧啶相互作用的第二种情况的发生概率。在这项工作中,我们描述了通过 MD 模拟生成的带有外翻尿嘧啶碱基的 DNA 结构,然后将其与 UDG 酶进行对接模拟。我们对 UDG-尿嘧啶识别复合物的研究结果支持这样一种观点,即 DNA 力学引起的碱基翻转可能是染色质中 UDG 糖基化酶识别尿嘧啶碱基的一种相关机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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