Suppr超能文献

连接功能分析阐明 RNA 结合蛋白的作用。

Tethered Function Assays to Elucidate the Role of RNA-Binding Proteins.

机构信息

Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Bern, Switzerland.

出版信息

Methods Mol Biol. 2022;2537:285-306. doi: 10.1007/978-1-0716-2521-7_17.

Abstract

The fate of each RNA molecule is strongly determined by RNA-binding proteins (RBPs) which accompany transcripts from its synthesis to its degradation. To elucidate the effect of a specific RBP on bound RNA, it can be artificially recruited to a specific site on a reporter mRNA that can be followed by a variety of methods. In this so-called tethering assay, the protein of interest (POI) is fused to the coat protein of the MS2 bacteriophage and expressed in your favorite cells together with a reporter gene containing MS2 binding sites. The MS2 binding sites are recognized by the MS2 coat protein (MS2CP) with high affinity and specificity and by doing so, the POI is tethered to the reporter RNA. Here, we describe how with the help of this assay the human cytoplasmic poly(A) binding protein is recruited to a mini-μ RNA reporter, thereby influencing the stability of the reporter transcript.

摘要

每个 RNA 分子的命运都受到 RNA 结合蛋白(RBPs)的强烈影响,这些蛋白伴随转录本从合成到降解的全过程。为了阐明特定 RBP 对结合 RNA 的影响,可以将其人工募集到报告 mRNA 上的特定部位,然后通过多种方法进行追踪。在这种所谓的连接测定中,感兴趣的蛋白质(POI)与 MS2 噬菌体的外壳蛋白融合,并与含有 MS2 结合位点的报告基因一起在您喜欢的细胞中表达。MS2 结合位点与 MS2 外壳蛋白(MS2CP)高度亲和且特异性结合,从而将 POI 连接到报告 RNA 上。在这里,我们描述了如何借助该测定法将细胞质多聚腺苷酸结合蛋白募集到 mini-μ RNA 报告基因上,从而影响报告转录本的稳定性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验