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A guanine-flipping and sequestration mechanism for G-quadruplex unwinding by RecQ helicases

机译:RecQ解旋酶用于G四链体退绕的鸟嘌呤翻转和螯合机制

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摘要

Homeostatic regulation of G-quadruplexes (G4s), four-stranded structures that can form in guanine-rich nucleic acids, requires G4 unwinding helicases. The mechanisms that mediate G4 unwinding remain unknown. We report the structure of a bacterial RecQ DNA helicase bound to resolved G4 DNA. Unexpectedly, a guanine base from the unwound G4 is sequestered within a guanine-specific binding pocket. Disruption of the pocket in RecQ blocks G4 unwinding, but not G4 binding or duplex DNA unwinding, indicating its essential role in structure-specific G4 resolution. A novel guanine-flipping and sequestration model that may be applicable to other G4-resolving helicases emerges from these studies.
机译:可以在富含鸟嘌呤的核酸中形成的四链结构G-四链体(G4)的稳态调节需要G4解旋解旋酶。调节G4释放的机制仍然未知。我们报告与解决的G4 DNA结合的细菌RecQ DNA解旋酶的结构。出乎意料的是,来自解绕的G4的鸟嘌呤碱基被螯合在鸟嘌呤特异性结合口袋中。 RecQ中口袋的破坏会阻止G4释放,但不会阻止G4结合或双链DNA释放,表明它在结构特异性G4解析中的重要作用。从这些研究中出现了一种新型的鸟嘌呤翻转和螯合模型,该模型可能适用于其他G4解析解旋酶。

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