Transcriptome-wide measurement of translation by ribosome profiling

被引:297
作者
McGlincy, Nicholas J. [1 ]
Ingolia, Nicholas T. [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Ctr RNA Syst Biol, Calif Inst Quantitat Biosci, 16 Barker Hall 3202, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
RNA; Translation; Ribosome; Ribosome profiling; High-throughput sequencing; RNA-sequencing; MESSENGER-RNA; MAMMALIAN-CELLS; IN-VIVO; REVEALS; VISUALIZATION; FOOTPRINT; ALIGNMENT; DYNAMICS; INSIGHTS;
D O I
10.1016/j.ymeth.2017.05.028
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Translation is one of the fundamental processes of life. It comprises the assembly of polypeptides whose amino acid sequence corresponds to the codon sequence of an mRNA's ORF. Translation is performed by the ribosome; therefore, in order to understand translation and its regulation we must be able to determine the numbers and locations of ribosomes on mRNAs in vivo. Furthermore, we must be able to examine their redistribution in different physiological contexts and in response to experimental manipulations. The ribosome profiling method provides us with an opportunity to learn these locations, by sequencing a cDNA library derived from the short fragments of mRNA covered by the ribosome. Since its original description, the ribosome profiling method has undergone continuing development; in this article we describe the method's current state. Important improvements include: the incorporation of sample barcodes to enable library multiplexing, the incorporation of unique molecular identifiers to enable to removal of duplicated sequences, and the replacement of a gel-purification step with the enzymatic degradation of unligated linker. (C) 2017 The Authors. Published by Elsevier Inc.
引用
收藏
页码:112 / 129
页数:18
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