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从尿嘧啶-DNA糖基化酶的结构研究结果中吸取的经验教训。

Lessons learned from structural results on uracil-DNA glycosylase.

作者信息

Parikh S S, Putnam C D, Tainer J A

机构信息

Department of Molecular Biology, Skaggs Institute for Chemical Biology, The Scripps Research Institute, MB4, 10550 North Torrey Pines Road, La Jolla, CA 92037-1027, USA.

出版信息

Mutat Res. 2000 Aug 30;460(3-4):183-99. doi: 10.1016/s0921-8777(00)00026-4.

Abstract

Uracil-DNA glycosylase (UDG) functions as a sentry guarding against uracil in DNA. UDG initiates DNA base excision repair (BER) by hydrolyzing the uracil base from the deoxyribose. As one of the best studied DNA glycosylases, a coherent and complete functional mechanism is emerging that combines structural and biochemical results. This functional mechanism addresses the detection of uracil bases within a vast excess of normal DNA, the features of the enzyme that drive catalysis, and coordination of UDG with later steps of BER while preventing the release of toxic intermediates. Many of the solutions that UDG has evolved to overcome the challenges of policing the genome are shared by other DNA glycosylases and DNA repair enzymes, and thus appear to be general.

摘要

尿嘧啶-DNA糖基化酶(UDG)起到防止DNA中出现尿嘧啶的哨兵作用。UDG通过水解脱氧核糖上的尿嘧啶碱基来启动DNA碱基切除修复(BER)。作为研究最深入的DNA糖基化酶之一,一种结合了结构和生化结果的连贯且完整的功能机制正在形成。这种功能机制涉及在大量正常DNA中检测尿嘧啶碱基、驱动催化作用的酶的特性,以及UDG与BER后续步骤的协调,同时防止有毒中间体的释放。UDG为克服监管基因组的挑战而进化出的许多解决方案也为其他DNA糖基化酶和DNA修复酶所共有,因此似乎具有普遍性。

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