首页> 美国卫生研究院文献>RNA >Site-specific crosslinking of human microRNPs to RNA targets
【2h】

Site-specific crosslinking of human microRNPs to RNA targets

机译:人类microRNP与RNA靶标的位点特异性交联

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

MicroRNAs (miRNAs) regulate the expression of numerous genes and are implicated in the pathogenesis of many human diseases. miRNAs act as specificity determinants to guide deposition of microRNPs (miRNPs) onto miRNA recognition elements (MREs) that are found in mRNA targets. We have adapted a site-specific crosslinking approach, previously used in the analysis of splicing, to interrogate protein factors that physically associate with MREs in human cells. We find that Ago proteins are the only proteins that bind to the MRE in a miRNA-dependent manner. Our method may be used in various experimental systems to analyze protein factors that influence MRE accessibility by miRNAs and the composition of MRE-bound miRNPs.
机译:微小RNA(miRNA)调节许多基因的表达,并与许多人类疾病的发病机制有关。 miRNA作为特异性决定因素,可指导将microRNP(miRNP)沉积到在mRNA靶标中发现的miRNA识别元件(MRE)上。我们已经调整了以前在剪接分析中使用的特定于站点的交联方法,以查询与人细胞中MRE物理相关的蛋白质因子。我们发现Ago蛋白是唯一以miRNA依赖性方式与MRE结合的蛋白。我们的方法可用于各种实验系统中,分析影响miRNA通过MRE接近MRE的蛋白质因子以及结合MRE的miRNP的成分。

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