Department of Molecular and Cell Biology, Center for RNA Systems Biology, California Institute for Quantitative Biosciences, University of California, Berkeley, 16 Barker Hall # 3202, Berkeley, CA 94720-3202, USA.
Methods. 2017 Aug 15;126:112-129. doi: 10.1016/j.ymeth.2017.05.028. Epub 2017 Jun 1.
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.
翻译是生命的基本过程之一。它包括将与 mRNA 的 ORF 的密码子序列相对应的多肽组装起来。翻译是由核糖体进行的;因此,为了理解翻译及其调控,我们必须能够确定核糖体在体内 mRNA 上的数量和位置。此外,我们必须能够检查它们在不同生理环境中的重新分布以及对实验操作的反应。核糖体分析方法通过对核糖体覆盖的短片段 mRNA 的 cDNA 文库进行测序,为我们提供了了解这些位置的机会。自最初描述以来,核糖体分析方法一直在不断发展;在本文中,我们描述了该方法的现状。重要的改进包括:加入样品条形码以实现文库的多重化,加入独特的分子标识符以去除重复序列,以及用酶促降解未连接的接头取代凝胶纯化步骤。