蛋白质与mRNA 3 '亚型的结合

Q2 Biochemistry, Genetics and Molecular Biology
Joseph V. Geisberg, Zarmik Moqtaderi
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引用次数: 1

摘要

在这里,我们描述了CLIP-READS,一种结合交联和免疫沉淀(CLIP)和3 '区提取和深度测序(READS)元素的技术,以提供mRNA 3 '异构体与给定信使核糖核蛋白(mRNP)结合的全基因组图谱。在CLIP-READS中,细胞生长到对数期,用紫外光(254 nm)照射形成rna -蛋白加合物。蛋白质- mRNA复合物是免疫沉淀的细胞提取物与特异性抗体感兴趣的蛋白质,之后的蛋白质成分被消化掉Pronase。信使rna随后受到3 ' READS的影响。由3 ' READS并行处理的输入样本允许通过感兴趣的mRNP对同种异构体特异性结合进行相对量化。©2019 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protein Binding to mRNA 3′ Isoforms

Here we describe CLIP-READS, a technique that combines elements of crosslinking and immunoprecipitation (CLIP) and 3′ region extraction and deep sequencing (READS), to provide a genome-wide map of mRNA 3′ isoform binding by a given messenger ribonucleoprotein (mRNP). In CLIP-READS, cells are grown to logarithmic phase and are irradiated with UV light (254 nm) to form RNA–protein adducts. The protein−mRNA complexes are immunoprecipitated from cell extracts with an antibody specific to the protein of interest, after which the protein component is digested away with Pronase. Messenger RNAs are then subjected to 3′ READS. An input sample processed by 3′ READS in parallel allows for the relative quantification of isoform-specific binding by the mRNP of interest. © 2019 by John Wiley & Sons, Inc.

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来源期刊
Current Protocols in Molecular Biology
Current Protocols in Molecular Biology Biochemistry, Genetics and Molecular Biology-Molecular Biology
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