...
首页> 外文期刊>Journal of Molecular Biology >THE ROLE OF DNA BENDING IN FLP-MEDIATED SITE-SPECIFIC RECOMBINATION
【24h】

THE ROLE OF DNA BENDING IN FLP-MEDIATED SITE-SPECIFIC RECOMBINATION

机译:DNA弯曲在FLP介导的位点重组中的作用

获取原文
获取原文并翻译 | 示例

摘要

The Flp recombinase of the 2 mu m 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. (C) 1995 Academic Press Limited [References: 53]
机译:酿酒酵母(Saccharomyces cerevisiae)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识别靶位点包含两个Flp结合序列,侧翼为8bp的核心区域。 Flp的结合导致形成两个Flp:DNA复合物(复合物I和II)。 Flp单体与单个对称元件的结合会产生约60度的DNA弯曲(I型弯曲),而两个Flp单体与FRT位点的结合会产生大于144度的DNA弯曲(II型弯曲)。我们已经使用循环置换分析来定位由Flp诱导的I型和II型DNA弯曲的中心,以及Flp肽P27(27 kDa;氨基酸残基124至346)和P32(32 kDa;氨基酸残基124至34)。 423)。 I型弯曲中心的位置取决于基材是否包含一个或两个Flp绑定元素。当基板包含一个对称元素时,由Flp引起的I型弯曲的中心位于b元素的芯-远端。但是,当底物包含两个Flp结合元素时,它位于b元素的核心近端。缺少Flp的NH2末端13 kDa区域的P27和P32肽没有显示这种行为。我们推断Flp的13 kDa区域对于将I型弯曲中心定位在最小的Flp识别位点上至关重要。我们提出了一个模型,其中Flp的单个分子与两个对称元素相互作用以解释这些结果。 Flp引起的II型弯曲的中心在核心区域的中间。我们使用连接缺陷的Flp蛋白来确定II型弯曲中心在上链或下链被切割的复合物中的位置。这种复合物的弯曲中心取决于哪条链被切割。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定义顺序相关联。 (C)1995 Academic Press Limited [参考号:53]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号