Simple and inexpensive ribosome profiling analysis of mRNA translation

被引:40
作者
Reid, David W. [1 ]
Shenolikar, Shirish [1 ,2 ]
Nicchitta, Christopher V. [3 ]
机构
[1] Duke NUS Grad Med Sch, Programme Cardiovasc & Metab Disorders, Singapore 169857, Singapore
[2] Duke NUS Grad Med Sch, Programme Neurosci & Behav Disorders, Singapore 169857, Singapore
[3] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
基金
英国医学研究理事会;
关键词
Ribosome profiling; Deep sequencing; mRNA; Transcriptomics; HUMAN GENOME; ENDOPLASMIC-RETICULUM; IN-VIVO; FRAGMENTS;
D O I
10.1016/j.ymeth.2015.07.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 74
页数:6
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