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通过 RNA 免疫沉淀翻译起始因子来测量翻译效率。

Measuring Translation Efficiency by RNA Immunoprecipitation of Translation Initiation Factors.

机构信息

Comparative Oncology Laboratory, University of California at Davis, Davis, CA, USA.

出版信息

Methods Mol Biol. 2021;2267:73-79. doi: 10.1007/978-1-0716-1217-0_5.

Abstract

Eukaryotic mRNAs are bound by a multitude of RNA binding proteins (RBPs) that control their localization, transport, and translation. Measuring the rate of translation of mRNAs is critical for understanding the factors and pathways involved in gene expression. In this chapter, we present a method to compare the rate of translation of individual mRNA species based on the fraction of mRNA bound by a specific ribonucleoprotein involved in the general translation machinery. The ribonucleoprotein complex is immunoprecipitated using an antibody for the RBP, followed by RT-PCR to semi-quantitatively determine the amount of an individual mRNA fraction bound by a translation regulating protein such as eIF4E.

摘要

真核生物的 mRNA 结合了大量 RNA 结合蛋白(RBPs),这些蛋白控制着它们的定位、运输和翻译。测量 mRNA 的翻译速度对于理解参与基因表达的因素和途径至关重要。在本章中,我们提出了一种方法,基于与一般翻译机制相关的特定核糖核蛋白结合的 mRNA 分数,来比较单个 mRNA 种类的翻译速度。使用针对 RBP 的抗体对核糖核蛋白复合物进行免疫沉淀,然后进行 RT-PCR,以半定量确定与翻译调节蛋白(如 eIF4E)结合的单个 mRNA 分数的量。

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