首页> 外文期刊>Nucleic Acids Research >Chromosomal transformation in Bacillus subtilis is a non-polar recombination reaction
【24h】

Chromosomal transformation in Bacillus subtilis is a non-polar recombination reaction

机译:枯草芽孢杆菌中的染色体转化是一种非极性重组反应

获取原文
获取原文并翻译 | 示例
           

摘要

Natural chromosomal transformation is one of the primary driving forces of bacterial evolution. This reaction involves the recombination of the internalized linear single-stranded (ss) DNA with the homologous resident duplex via RecA-mediated integration in concert with SsbA and DprA or RecO. We show that sequence divergence prevents Bacillus subtilis chromosomal transformation in a log-linear fashion, but it exerts a minor effect when the divergence is localized at a discrete end. In the nucleotide bound form, RecA shows no apparent preference to initiate recombination at the 3'- or 5'-complementary end of the linear duplex with circular ssDNA, but nucleotide hydrolysis is required when heterology is present at both ends. RecA center dot dATP initiates pairing of the linear 5' and 3' complementary ends, but only initiation at the 5'-end remains stably paired in the absence of SsbA. Our results suggest that during gene transfer RecA center dot ATP, in concert with SsbA and DprA or RecO, shows a moderate preference for the 3'-end of the duplex. We show that RecA-mediated recombination initiated at the 3'- or 5'-complementary end might have significant implication on the ecological diversification of bacterial species with natural transformation.
机译:天然染色体转化是细菌进化的主要驱动力之一。该反应涉及通过与SsbA和DprA或RecO协同的RecA介导的整合,使内化的线性单链(ss)DNA与同源的驻留双链体重组。我们表明,序列差异阻止了枯草芽孢杆菌的染色体转化,以对数线性方式,但是当差异位于离散末端时,它发挥了较小的作用。在核苷酸结合形式中,RecA没有明显的偏好在环状双链体的3'-或5'-互补端起始与环状ssDNA的重组,但是当两端均存在异源时,则需要进行核苷酸水解。 RecA中心点dATP启动线性5'和3'互补末端的配对,但只有在5'末端的起始在没有SsbA的情况下仍保持稳定配对。我们的结果表明,在基因转移过程中,RecA中心点ATP与SsbA和DprA或RecO协同作用,显示出对双链体3'端的中等偏爱。我们显示,RecA介导的重组始于3'-或5'-互补端,可能对具有自然转化的细菌物种的生态多样性产生重大影响。

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