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对mRNA翻译进行简单且经济的核糖体谱分析。

Simple and inexpensive ribosome profiling analysis of mRNA translation.

作者信息

Reid David W, Shenolikar Shirish, Nicchitta Christopher V

机构信息

Programme in Cardiovascular and Metabolic Disorders, Duke-NUS Graduate Medical School, Singapore 169857, Singapore.

Programme in Cardiovascular and Metabolic Disorders, Duke-NUS Graduate Medical School, Singapore 169857, Singapore; Programme in Neuroscience and Behavioral Disorders, Duke-NUS Graduate Medical School, Singapore 169857, Singapore.

出版信息

Methods. 2015 Dec;91:69-74. doi: 10.1016/j.ymeth.2015.07.003. Epub 2015 Jul 8.

Abstract

The development and application of ribosome profiling has markedly advanced our understanding of ribosomes and mRNA translation. The experimental approach, which relies on deep sequencing of ribosome-protected mRNA fragments generated by treatment of polyribosomes with exogenous nucleases, provides a transcriptome-wide assessment of translation. The broad application of ribosome profiling has been slowed by the complexity and expense of the protocol. Here, we provide a simplified ribosome profiling method that uses micrococcal nuclease to generate ribosome footprints in crude cellular extracts, which are then purified simply by size selection via polyacrylamide gel electrophoresis. This simplification removes the laborious or expensive purification of ribosomes that has typically been used. This direct extraction method generates gene-level ribosome profiling data that are similar to a method that includes ribosome purification. This protocol should significantly ease the barrier to entry for research groups interested in employing ribosome profiling.

摘要

核糖体谱分析技术的发展与应用显著推进了我们对核糖体及mRNA翻译的理解。该实验方法依赖于对用外源核酸酶处理多核糖体所产生的核糖体保护的mRNA片段进行深度测序,从而提供全转录组范围的翻译评估。核糖体谱分析技术的广泛应用因该实验方案的复杂性和成本而受到阻碍。在此,我们提供一种简化的核糖体谱分析方法,该方法使用微球菌核酸酶在粗细胞提取物中生成核糖体足迹,然后通过聚丙烯酰胺凝胶电泳简单地按大小选择进行纯化。这种简化省去了通常使用的繁琐且昂贵的核糖体纯化步骤。这种直接提取方法所生成的基因水平的核糖体谱分析数据与包括核糖体纯化的方法相似。该实验方案应能显著降低有意采用核糖体谱分析技术的研究团队的入门门槛。

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