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DNA弯曲在Flp介导的位点特异性重组中的作用。

The role of DNA bending in Flp-mediated site-specific recombination.

作者信息

Luetke K H, Sadowski P D

机构信息

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

出版信息

J Mol Biol. 1995 Aug 25;251(4):493-506. doi: 10.1006/jmbi.1995.0451.

Abstract

The Flp recombinase of the 2 micron plasmid of Saccharomyces cerevisiae binds to a recognition target site, induces DNA bending and catalyses DNA cleavage and strand exchange to bring about recombination. The minimal Flp recognition target site contains two Flp binding sequences flanking an 8 bp core region; binding of Flp results in the formation of two Flp:DNA complexes (complexes I and II). Binding of a Flp monomer to a single symmetry element generates a DNA bend of about 60 degrees (a type I bend), whereas binding of two Flp monomers to the FRT site generates a DNA bend of > 144 degrees (a type II bend). We have used circular permutation analysis to locate the centre of the type I and type II DNA bends induced by Flp, and the Flp peptides P27 (27 kDa; amino acid residues 124 to 346) and P32 (32 kDa; amino acid residues 124 to 423). The location of the centre of the type I bend depends upon whether the substrate contains one or two Flp binding elements. When the substrate contains one symmetry element, the centre of the type I bend induced by Flp is located at the core-distal end of the b element. However, it is located at the core-proximal end of the b element when the substrate contains two Flp-binding elements. The P27 and P32 peptides, which lack the NH2-terminal 13 kDa region of Flp, do not show this behaviour. We deduce that the 13 kDa region of Flp is critical for the positioning of the type I bend centre on a minimal Flp recognition site. We propose a model in which a single molecule of Flp interacts with two symmetry elements to account for these results. The centre of the type II bend induced by Flp is in the middle of the core region. We used ligation-defective Flp proteins to determine the location of the type II bend centres in complexes where either the top or bottom strand was cleaved. The bend centres of such complexes depend upon which strand is cleaved. We propose a model which associates the position of Flp-induced type II bends with a defined order of strand exchanges in the recombination reaction.

摘要

酿酒酵母2μm质粒的Flp重组酶与识别靶位点结合,诱导DNA弯曲,并催化DNA切割和链交换以实现重组。最小的Flp识别靶位点在一个8bp的核心区域两侧包含两个Flp结合序列;Flp的结合导致形成两个Flp:DNA复合物(复合物I和II)。一个Flp单体与单个对称元件的结合产生约60度的DNA弯曲(I型弯曲),而两个Flp单体与FRT位点的结合产生大于144度的DNA弯曲(II型弯曲)。我们使用环形置换分析来定位由Flp以及Flp肽P27(27kDa;氨基酸残基124至346)和P32(32kDa;氨基酸残基124至423)诱导的I型和II型DNA弯曲的中心。I型弯曲中心的位置取决于底物包含一个还是两个Flp结合元件。当底物包含一个对称元件时,由Flp诱导的I型弯曲中心位于b元件的核心远端。然而,当底物包含两个Flp结合元件时,它位于b元件的核心近端。缺少Flp的NH2末端13kDa区域的P27和P32肽不表现出这种行为。我们推断Flp的13kDa区域对于I型弯曲中心在最小Flp识别位点上的定位至关重要。我们提出了一个模型,其中单个Flp分子与两个对称元件相互作用来解释这些结果。由Flp诱导的II型弯曲中心位于核心区域的中间。我们使用连接缺陷型Flp蛋白来确定在顶部或底部链被切割的复合物中II型弯曲中心的位置。此类复合物的弯曲中心取决于切割的是哪条链。我们提出了一个模型,该模型将Flp诱导的II型弯曲的位置与重组反应中链交换的特定顺序相关联。

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