Abstract

The initiation of translation is a fundamental and highly regulated process in gene expression. Translation initiation in prokaryotic systems usually requires interaction between the ribosome and an mRNA sequence upstream of the initiation codon, the so-called ribosome-binding site (Shine-Dalgarno sequence). However, a large number of genes do not possess Shine-Dalgarno sequences, and it is unknown how start codon recognition occurs in these mRNAs. We have performed genome-wide searches in various groups of prokaryotes in order to identify sequence elements and/or RNA secondary structural motifs that could mediate translation initiation in mRNAs lacking Shine-Dalgarno sequences. We find that mRNAs without a Shine-Dalgarno sequence are generally less structured in their translation initiation region and show a minimum of mRNA folding at the start codon. Using reporter gene constructs in bacteria, we also provide experimental support for local RNA unfoldedness determining start codon recognition in Shine-Dalgarno–independent translation. Consistent with this, we show that AUG start codons reside in single-stranded regions, whereas internal AUG codons are usually in structured regions of the mRNA. Taken together, our bioinformatics analyses and experimental data suggest that local absence of RNA secondary structure is necessary and sufficient to initiate Shine-Dalgarno–independent translation. Thus, our results provide a plausible mechanism for how the correct translation initiation site is recognized in the absence of a ribosome-binding site.

Highlights

  • Shine-Dalgarno (SD) sequences reside in the 59 untranslated region (59 UTR) of prokaryotic messenger RNAs and facilitate translation initiation

  • While we find no evidence for alternative sequence motifs or secondary structural requirements, we have discovered that mRNAs lacking an SD sequence exhibit a pronounced minimum in mRNA secondary structure at the translational start codon, suggesting that start codon accessibility is the major factor in SD-independent translation initiation

  • Initiation of translation depends on molecular recognition of the messenger RNA by ribosomes. In prokaryotes, this recognition is mediated by a specific sequence motif in the 59 untranslated region of the mRNA, called ‘‘ribosome-binding site’’ or ‘‘Shine-Dalgarno sequence.’’ many messenger RNAs lack Shine-Dalgarno sequences, and it is currently unknown how the correct translation initiation site is recognized in these mRNAs

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Summary

Introduction

Shine-Dalgarno (SD) sequences reside in the 59 untranslated region (59 UTR) of prokaryotic messenger RNAs and facilitate translation initiation. They act as ribosome-binding sites by recognizing a sequence motif at the 39 end of the 16S ribosomal RNA in the 30S ribosomal subunit (referred to as anti-ShineDalgarno sequence, ASD) via complementary base pairing [1,2]. The SD-ASD interaction is conserved across the prokaryotic kingdom and has even been retained in some cell organelles that evolved from prokaryotes more than a billion years ago. Tobacco plastids (chloroplasts) and the c-proteobacterium Escherichia coli have identical ASD sequences in the 39 end of their 16S ribosomal RNAs (59 TGGATCACCTCCTT 39; ASD motif underlined) and, plastid SD sequences can be recognized in E. coli and vice versa [3,4]. The conserved spacing determined for E. coli is 49 nucleotides

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