首页> 外文期刊>FEBS Open Bio >miR‐127‐5p negatively regulates enterovirus 71 replication by directly targeting SCARB2
【24h】

miR‐127‐5p negatively regulates enterovirus 71 replication by directly targeting SCARB2

机译:miR‐127-5p通过直接靶向SCARB2负调控肠病毒71复制

获取原文
获取外文期刊封面目录资料

摘要

Enterovirus 71 (EV71) is the major causative agent of hand‐foot‐and‐mouth disease in young children and can cause severe cerebral and pulmonary complications and even fatality. This study aimed at elucidating whether and how EV71 infection is regulated by a cellular microRNA, miR‐127‐5p. We found that miR‐127‐5p can downregulate the expression of SCARB2, a main receptor of EV71, by targeting two potential sites in its 3′ UTR region and inhibit EV71 infection. Meanwhile, miR‐127‐5p expression was upregulated during EV71 infection. Notably, transfecting cells with miR‐127‐5p mimics led to a significant decrease in viral replication, while inhibition of endogenous miR‐127‐5p facilitated viral replication. Furthermore, our evidence showed that miR‐127‐5p did not affect postentry viral replication. Taken together, these results indicated that miR‐127‐5p inhibited EV71 replication by targeting the SCARB2 mRNA.
机译:肠病毒71(EV71)是幼儿手足口病的主要病原体,可导致严重的脑部和肺部并发症甚至死亡。这项研究旨在阐明是否以及如何通过细胞microRNA miR-127-5p调节EV71感染。我们发现miR‐127-5p可以通过靶向EV71的3'UTR区域中的两个潜在位点并抑制EV71感染来下调EV71的主要受体SCARB2的表达。同时,在EV71感染期间,miR-127-5p表达上调。值得注意的是,用miR-127-5p模拟物转染细胞会导致病毒复制显着减少,而抑制内源性miR-127-5p会促进病毒复制。此外,我们的证据表明miR-127-5p不会影响进入后的病毒复制。综上所述,这些结果表明miR‐127-5p通过靶向SCARB2 mRNA抑制了EV71复制。

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