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酿酒酵母2微米环状质粒的FLP重组酶使其DNA靶点弯曲。分离出在DNA弯曲方面有缺陷的FLP突变体。

FLP recombinase of the 2 microns circle plasmid of Saccharomyces cerevisiae bends its DNA target. Isolation of FLP mutants defective in DNA bending.

作者信息

Schwartz C J, Sadowski P D

机构信息

Department of Medical Genetics, University of Toronto, Ontario, Canada.

出版信息

J Mol Biol. 1989 Feb 20;205(4):647-58. doi: 10.1016/0022-2836(89)90310-0.

Abstract

The FLP recombinase is encoded by the yeast plasmid 2 microns circle and catalyses a site-specific recombination reaction that results in inversion of a segment of the 2 micron plasmid. We describe a method for the isolation of inactivating mutations in the FLP gene. The analysis of the recombination and binding activity of defective FLP proteins in vitro resulted in the identification of two classes of mutations: those that completely abolish FLP function by interfering with DNA binding and others that block recombination after the binding step. We have shown that FLP-mediated recombination is accompanied by bending of the DNA target and that mutations in the FLP recombinase that block bending also eliminate recombination.

摘要

FLP重组酶由酵母质粒2微米环编码,催化位点特异性重组反应,导致2微米质粒的一段发生倒位。我们描述了一种分离FLP基因失活突变的方法。对有缺陷的FLP蛋白在体外的重组和结合活性进行分析,鉴定出两类突变:一类通过干扰DNA结合完全消除FLP功能,另一类在结合步骤后阻断重组。我们已经表明,FLP介导的重组伴随着DNA靶标的弯曲,并且FLP重组酶中阻断弯曲的突变也消除了重组。

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