4.7 Article

Transcriptome-wide measurement of translation by ribosome profiling

期刊

METHODS
卷 126, 期 -, 页码 112-129

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2017.05.028

关键词

RNA; Translation; Ribosome; Ribosome profiling; High-throughput sequencing; RNA-sequencing

资金

  1. National Institutes of Health [R21 ES022575, P50 GM102706, DP2 CA195768]
  2. Glenn Foundation for Medical Research
  3. NIH [S10 OD018174]

向作者/读者索取更多资源

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.

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