首页> 美国卫生研究院文献>Nucleic Acids Research >Effect of DNA bending in various regions of a consensus-like Escherichia coli promoter on its strength in vivo and structure of the open complex in vitro.
【2h】

Effect of DNA bending in various regions of a consensus-like Escherichia coli promoter on its strength in vivo and structure of the open complex in vitro.

机译:DNA在共有型大肠杆菌启动子的各个区域弯曲对其体内强度和体外开放复合物结构的影响。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A series of E. coli promoters made of the consensus -35 and -10 hexamers separated by 17 bp spacer with variously located bending dTn.dAn, n = 5 or 6, sequences was constructed and cloned into the plasmid pDS3. Electrophoretic gel mobilities of restriction fragments containing these promoters correlated with the number of the T tracts encoded in the promoter sequences. The open complexes formed by E. coli RNA polymerase on promoters containing the T5(-34...-38) tract exhibited gel retardation indicative of their different gross geometry. The strength of these promoters measured in vivo in relation to an internal transcriptional standard was shown to be significantly lower than that of the group without the T5(-34...-38) tract. Within both these groups the promoters with two T6 tracts in the spacer, aligned in phase with the B-DNA helix repeat, had lower transcriptional activity, while the T6 tract encoded in the -7...-2 promoter region apparently had no influence on the strength of the respective promoters.
机译:构建了一系列由共有的-35和-10六聚体组成的大肠杆菌启动子,这些启动子被17 bp间隔物隔开,弯曲位置dTn.dAn,n = 5或6,序列不同,并将其克隆到质粒pDS3中。含有这些启动子的限制性片段的电泳凝胶迁移率与在启动子序列中编码的T束的数目有关。大肠杆菌RNA聚合酶在含有T5(-34 ...- 38)的启动子上形成的开放复合物显示出凝胶阻滞,表明它们的总体几何形状不同。相对于内部转录标准,这些启动子的体内强度显示出显着低于没有T5(-34 ...- 38)束的组。在这两个组中,间隔区中具有与B-DNA螺旋重复序列同相排列的两个T6通道的启动子具有较低的转录活性,而在-7 ...- 2启动子区域中编码的T6通道显然没有影响取决于各自促进者的力量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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