首页> 美国卫生研究院文献>PLoS Clinical Trials >Nuclear Translocation of Acinetobacter baumannii Transposase Induces DNA Methylation of CpG Regions in the Promoters of E-cadherin Gene
【2h】

Nuclear Translocation of Acinetobacter baumannii Transposase Induces DNA Methylation of CpG Regions in the Promoters of E-cadherin Gene

机译:鲍曼不动杆菌转座酶的核易位诱导E-钙粘蛋白基因启动子中CpG区的DNA甲基化

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

Nuclear targeting of bacterial proteins has emerged as a pathogenic mechanism whereby bacterial proteins induce host cell pathology. In this study, we examined nuclear targeting of Acinetobacter baumannii transposase (Tnp) and subsequent epigenetic changes in host cells. Tnp of A. baumannii ATCC 17978 possesses nuclear localization signals (NLSs), 225RKRKRK230. Transient expression of A. baumannii Tnp fused with green fluorescent protein (GFP) resulted in the nuclear localization of these proteins in COS-7 cells, whereas the truncated Tnp without NLSs fused with GFP were exclusively localized in the cytoplasm. A. baumannii Tnp was found in outer membrane vesicles, which delivered this protein to the nucleus of host cells. Nuclear expression of A. baumannii Tnp fused with GFP in A549 cells induced DNA methylation of CpG regions in the promoters of E-cadherin (CDH1) gene, whereas the cytoplasmic localization of the truncated Tnp without NLSs fused with GFP did not induce DNA methylation. DNA methylation in the promoters of E-cadherin gene induced by nuclear targeting of A. baumannii Tnp resulted in down-regulation of gene expression. In conclusion, our data show that nuclear traffic of A. baumannii Tnp induces DNA methylation of CpG regions in the promoters of E-cadherin gene, which subsequently down-regulates gene expression. This study provides a new insight into the epigenetic control of host genes by bacterial proteins.
机译:细菌蛋白的核靶向已成为一种致病机制,细菌蛋白可诱导宿主细胞病理。在这项研究中,我们检查了鲍曼不动杆菌转座酶(Tnp)的核定靶以及随后宿主细胞的表观遗传变化。鲍曼不动杆菌ATCC 17978的Tnp拥有核定位信号(NLSs)225RKRKRK230。融合有绿色荧光蛋白(GFP)的鲍曼不动杆菌Tnp的瞬时表达导致这些蛋白在COS-7细胞中的核定位,而不含NLS的截短的Tnp与GFP融合仅定位在细胞质中。在外膜囊泡中发现了鲍曼不动杆菌Tnp,该蛋白将这种蛋白传递到宿主细胞的核中。鲍曼不动杆菌Tnp与GFP融合在A549细胞中的核表达可诱导E-钙粘蛋白(CDH1)基因启动子中CpG区的DNA甲基化,而无NLSs的截短Tnp的胞质定位则不诱导DNA甲基化。鲍曼不动杆菌Tnp的核靶向诱导E-钙粘着蛋白基因启动子中的DNA甲基化导致基因表达下调。总之,我们的数据表明鲍曼不动杆菌Tnp的核运输诱导E-钙粘蛋白基因启动子中CpG区的DNA甲基化,从而下调基因表达。这项研究为细菌蛋白对宿主基因的表观遗传控制提供了新的见识。

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