Related Experiment Video
Updated: Jul 10, 2026

Determination of the Optimal Chromosomal Location(s) for a DNA Element in Escherichia coli Using a Novel Transposon-mediated Approach
Published on: September 11, 2017
Translation initiation region sequence preferences in Escherichia coli
Vladimir Vimberg1, Age Tats, Maido Remm
1Institute of Technology, University of Tartu, Nooruse 1, Tartu 50411, Estonia. riboloom@hot.ee
The optimal Shine-Dalgarno (SD) sequence length for bacterial translation initiation is six nucleotides. AU-rich enhancers significantly boost translation efficiency, especially when combined with strong SD sequences.
Area of Science:
- Bacterial molecular biology
- Gene expression regulation
Background:
- The mRNA translation initiation region (TIR) includes the initiator codon, Shine-Dalgarno (SD) sequence, and translational enhancers.
- A/U-rich sequences are a common class of translational enhancers.
Purpose of the Study:
- To investigate the impact of SD sequence length and enhancer presence on translation initiation efficiency.
- To understand the interplay between SD sequences, enhancers, and bacterial growth conditions.
Main Methods:
- Experimental testing of varying SD sequence lengths and enhancer presence.
- In silico analysis of TIRs in E. coli mRNAs.
Main Results:
- A six-nucleotide SD sequence (AGGAGG) is most efficient at 37°C.
- A/U-rich enhancers significantly stimulate translation, particularly during the bacterial exponential growth phase.
- SD sequences and enhancers exhibit cooperative effects, with strong SDs showing greater enhancement.
- Bacterial growth temperature influences TIR selection, favoring shorter SD sequences at lower temperatures.
- No significant correlation was found between SD sequence base-pairing potential and codon adaptation index in E. coli.
Conclusions:
- In E. coli, Shine-Dalgarno sequence selection is primarily influenced by growth temperature, not growth rate.
- A/U-rich enhancers substantially enhance translation by acting cooperatively with SD sequences.
Related Concept Videos
Leaky Scanning
Initiation of Translation
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
Translation in Prokaryotes
Prokaryotic Gene Structure and Organization
Mismatch Repair
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Translational Regulation

