Translation & the Genetic Code

the Shine-Dalgarno sequence

/ SHYNE dal-GAR-no /

A bacterium's ribosome cannot just scan an mRNA from its tip looking for a start codon — bacterial mRNAs often have no convenient end to begin at, and several genes can sit on one mRNA. So how does the ribosome find each gene's AUG? It looks for a short landmark a few bases upstream, the Shine-Dalgarno sequence, which acts like a signpost reading 'start codon just ahead'.

The Shine-Dalgarno sequence is a short purine-rich stretch, classically something like AGGAGG, sitting roughly five to ten bases before the start codon. Its trick is direct base-pairing: the very end of the ribosome's small-subunit RNA (the 16S ribosomal RNA) carries a complementary sequence, and the two zip together. This pairing parks the small subunit at exactly the right distance so that the start AUG falls into the P site, fixing the reading frame in one move. It is found in bacteria and archaea, and it is part of why bacterial translation can begin in the middle of a long mRNA, not only at its end.

This is one of the cleanest differences between bacterial and eukaryotic translation, and it has real consequences. Because several Shine-Dalgarno-plus-AUG units can sit along one bacterial mRNA, a single bacterial mRNA can encode several proteins (a polycistronic message) — something eukaryotic scanning generally cannot do. For genetic engineers, supplying a strong Shine-Dalgarno sequence is a standard way to make bacteria pump out lots of a desired protein. Eukaryotes have no Shine-Dalgarno sequence; they find the start codon by the entirely different cap-and-scan route.

A bacterial mRNA reading 5'-...AGGAGG-(7 bases)-AUG...-3' has its Shine-Dalgarno (AGGAGG) base-pair with the 16S rRNA's tail, positioning the ribosome so that the downstream AUG lands in the P site.

The SD sequence base-pairs with rRNA to position the start codon in the P site.

The Shine-Dalgarno sequence is a bacterial/archaeal feature. Eukaryotes lack it entirely and instead scan from the 5' cap, which is one reason bacterial mRNAs can be polycistronic and eukaryotic ones usually are not.

Also called
SD sequenceribosome binding siteRBS核糖体结合位点核糖體結合位點