首页> 美国卫生研究院文献>BMC Molecular Biology >Short-term cytotoxic effects and long-term instability of RNAi delivered using lentiviral vectors
【2h】

Short-term cytotoxic effects and long-term instability of RNAi delivered using lentiviral vectors

机译:使用慢病毒载体递送的RNAi的短期细胞毒性作用和长期不稳定性

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

BackgroundRNA interference (RNAi) can potently reduce target gene expression in mammalian cells and is in wide use for loss-of-function studies. Several recent reports have demonstrated that short double-stranded RNAs (dsRNAs), used to mediate RNAi, can also induce an interferon-based response resulting in changes in the expression of many interferon-responsive genes. Off-target gene silencing has also been described, bringing into question the validity of certain RNAi-based approaches for studying gene function. We have targeted the plasminogen activator inhibitor-2 (PAI-2 or SERPINB2) mRNA using lentiviral vectors for delivery of U6 promoter-driven PAI-2-targeted short hairpin RNA (shRNA) expression. PAI-2 is reported to have anti-apoptotic activity, thus reduction of endogenous expression may be expected to make cells more sensitive to programmed cell death.
机译:背景技术RNA干扰(RNAi)可以有效地降低哺乳动物细胞中靶基因的表达,并广泛用于功能丧失研究。最近的几篇报道表明,用于介导RNAi的短双链RNA(dsRNA)也可以诱导基于干扰素的应答,从而导致许多干扰素应答基因的表达发生变化。还描述了脱靶基因沉默,这使某些基于RNAi的方法研究基因功能的有效性受到质疑。我们已使用慢病毒载体靶向纤溶酶原激活物抑制剂2(PAI-2或SERPINB2)mRNA,以递送U6启动子驱动的PAI-2-靶向短发夹RNA(shRNA)表达。据报道,PAI-2具有抗凋亡活性,因此内源性表达的降低有望使细胞对程序性细胞死亡更加敏感。

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