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本文引用的文献

1
Implications for switching restriction enzyme specificities from the structure of BstYI bound to a BglII DNA sequence.基于与BglII DNA序列结合的BstYI结构对切换限制酶特异性的启示。
Structure. 2005 May;13(5):791-801. doi: 10.1016/j.str.2005.02.018.
2
Structure of HinP1I endonuclease reveals a striking similarity to the monomeric restriction enzyme MspI.HinP1I核酸内切酶的结构显示出与单体限制性酶MspI惊人的相似性。
Nucleic Acids Res. 2005 Apr 1;33(6):1892-901. doi: 10.1093/nar/gki337. Print 2005.
3
Type II restriction endonucleases: structure and mechanism.II型限制性核酸内切酶:结构与机制
Cell Mol Life Sci. 2005 Mar;62(6):685-707. doi: 10.1007/s00018-004-4513-1.
4
A homology model of restriction endonuclease SfiI in complex with DNA.限制性内切酶SfiI与DNA复合物的同源模型。
BMC Struct Biol. 2005 Jan 24;5:2. doi: 10.1186/1472-6807-5-2.
5
REBASE--restriction enzymes and DNA methyltransferases.REBASE——限制性内切酶和DNA甲基转移酶。
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D230-2. doi: 10.1093/nar/gki029.
6
An asymmetric complex of restriction endonuclease MspI on its palindromic DNA recognition site.限制性内切酶MspI在其回文DNA识别位点上的不对称复合物。
Structure. 2004 Sep;12(9):1741-7. doi: 10.1016/j.str.2004.07.014.
7
Dynamics of DNA loop capture by the SfiI restriction endonuclease on supercoiled and relaxed DNA.SfiI限制性内切核酸酶对超螺旋和松弛DNA的DNA环捕获动力学
J Mol Biol. 2004 May 21;339(1):53-66. doi: 10.1016/j.jmb.2004.03.046.
8
Crystal structure of BstYI at 1.85A resolution: a thermophilic restriction endonuclease with overlapping specificities to BamHI and BglII.分辨率为1.85埃的嗜热限制性内切酶BstYI的晶体结构:对BamHI和BglII具有重叠特异性的嗜热限制性内切酶。
J Mol Biol. 2004 May 7;338(4):725-33. doi: 10.1016/j.jmb.2004.02.074.
9
3DNA: a software package for the analysis, rebuilding and visualization of three-dimensional nucleic acid structures.3DNA:一个用于三维核酸结构分析、重建和可视化的软件包。
Nucleic Acids Res. 2003 Sep 1;31(17):5108-21. doi: 10.1093/nar/gkg680.
10
Crystallization of restriction endonuclease SfiI in complex with DNA.限制性内切酶SfiI与DNA复合物的结晶。
Acta Crystallogr D Biol Crystallogr. 2003 Aug;59(Pt 8):1493-5. doi: 10.1107/s0907444903011910. Epub 2003 Jul 23.

结合DNA的四聚体内切酶SfiI结构所呈现的连续结合事件。

A view of consecutive binding events from structures of tetrameric endonuclease SfiI bound to DNA.

作者信息

Vanamee Eva Scheuring, Viadiu Hector, Kucera Rebecca, Dorner Lydia, Picone Stephen, Schildkraut Ira, Aggarwal Aneel K

机构信息

Structural Biology Program, Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

EMBO J. 2005 Dec 7;24(23):4198-208. doi: 10.1038/sj.emboj.7600880. Epub 2005 Nov 24.

DOI:10.1038/sj.emboj.7600880
PMID:16308566
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1356319/
Abstract

Many reactions in cells proceed via the sequestration of two DNA molecules in a synaptic complex. SfiI is a member of a growing family of restriction enzymes that can bind and cleave two DNA sites simultaneously. We present here the structures of tetrameric SfiI in complex with cognate DNA. The structures reveal two different binding states of SfiI: one with both DNA-binding sites fully occupied and the other with fully and partially occupied sites. These two states provide details on how SfiI recognizes and cleaves its target DNA sites, and gives insight into sequential binding events. The SfiI recognition sequence (GGCCNNNN[downward arrow]NGGCC) is a subset of the recognition sequence of BglI (GCCNNNN[downward arrow]NGGC), and both enzymes cleave their target DNAs to leave 3-base 3' overhangs. We show that even though SfiI is a tetramer and BglI is a dimer, and there is little sequence similarity between the two enzymes, their modes of DNA recognition are unusually similar.

摘要

细胞中的许多反应是通过在突触复合物中隔离两个DNA分子来进行的。SfiI是一个不断增加的限制酶家族的成员,它可以同时结合并切割两个DNA位点。我们在此展示了与同源DNA结合的四聚体SfiI的结构。这些结构揭示了SfiI的两种不同结合状态:一种是两个DNA结合位点都被完全占据,另一种是位点被完全和部分占据。这两种状态提供了关于SfiI如何识别和切割其靶DNA位点的详细信息,并深入了解了连续的结合事件。SfiI识别序列(GGCCNNNN[向下箭头]NGGCC)是BglI识别序列(GCCNNNN[向下箭头]NGGC)的一个子集,并且这两种酶都切割它们的靶DNA以留下3个碱基的3'突出端。我们表明,尽管SfiI是四聚体而BglI是二聚体,并且这两种酶之间几乎没有序列相似性,但它们的DNA识别模式异常相似。