| Literature DB >> 30346115 |
Ben B Li1,2, Changli Qian1, Thomas M Roberts1, Jean J Zhao1,2.
Abstract
This unit describes a reverse transcription-quantitative PCR (RT-qPCR)-based method for gene-targeted measurement of RNA translation levels. The method includes washing and lysing cells with a buffer containing cycloheximide to enrich ribosomal accumulation at translation initiation sites (TIS), followed by enzymatic treatment to generate ribosomal footprints, reverse transcription targeted towards TIS of specific transcripts of interest to generate complementary DNA (cDNA), and qPCR to measure the abundance of these footprints. This method enables time- and cost-effective assessment of changes in translation levels across focused panels of genes and across numerous samples.Entities:
Keywords: RNA translation; RT-qPCR; protein synthesis
Mesh:
Substances:
Year: 2018 PMID: 30346115 PMCID: PMC6326074 DOI: 10.1002/cpmb.71
Source DB: PubMed Journal: Curr Protoc Mol Biol ISSN: 1934-3647