A combination of mRNA features influence the efficiency of leaderless mRNA translation initiation. (23rd September 2021)

• Record Type: Journal Article
• Authors: Bharmal, Mohammed-Husain M; Gega, Alisa; Schrader, Jared M
• Is Part Of: NAR genomics and bioinformatics. Volume 3:issue 3(2021)
• Publication Date: 2021-09-23
• Subjects: Genomics -- Periodicals; Bioinformatics -- Periodicals; 572.8
• DOI: 10.1093/nargab/lqab081
• Languages: English
• ISSNs: 2631-9268

Abstract

Abstract: Bacterial translation is thought to initiate by base pairing of the 16S rRNA and the Shine–Dalgarno sequence in the mRNA's 5′ untranslated region (UTR). However, transcriptomics has revealed that leaderless mRNAs, which completely lack any 5′ UTR, are broadly distributed across bacteria and can initiate translation in the absence of the Shine–Dalgarno sequence. To investigate the mechanism of leaderless mRNA translation initiation, synthetic in vivo translation reporters were designed that systematically tested the effects of start codon accessibility, leader length, and start codon identity on leaderless mRNA translation initiation. Using these data, a simple computational model was built based on the combinatorial relationship of these mRNA features that can accurately classify leaderless mRNAs and predict the translation initiation efficiency of leaderless mRNAs. Thus, start codon accessibility, leader length, and start codon identity combine to define leaderless mRNA translation initiation in bacteria.