Direct analysis of ribosome targeting illuminates thousand-fold regulation of translation initiation

Abstract

Translational control shapes the proteome in normal and pathophysiological conditions. Current high-throughput approaches reveal large differences in mRNA-specific translation activity but cannot identify the causative mRNA features. We developed direct analysis of ribosome targeting (DART) and used it to dissect regulatory elements within 5' untranslated regions that confer thousand-fold differences in ribosome recruitment in biochemically accessible cell lysates. Using DART, we identified novel translational enhancers and silencers, determined a functional role for most alternative 5' UTR isoforms expressed in yeast, and revealed a general mode of increased translation via direct binding to a core translation factor. DART enables systematic assessment of the translational regulatory potential of 5' UTR variants, whether native or disease-associated, and will facilitate engineering of mRNAs for optimized protein production in various systems. HighlightsO_LIDART illuminates thousand-fold differences in 5' UTR-specific translation activity C_LIO_LISNPs and alternative 5' UTR isoforms affect ribosome recruitment significantly C_LIO_LIInhibitory effects of RNA structures are highly dependent on 5' UTR context C_LIO_LI5' UTR motifs bind initiation factors directly, broadly stimulating translation C_LI