Larsen B, Wills N M, Gesteland R F, Atkins J F
Howard Hughes Medical Institute, University of Utah, Salt Lake City 84112.
J Bacteriol. 1994 Nov;176(22):6842-51. doi: 10.1128/jb.176.22.6842-6851.1994.
Base pairing between the 3' end of 16S rRNA and mRNA is shown to be important for the programmed -1 frameshifting utilized in decoding the Escherichia coli dnaX gene. This pairing is the same as the Shine-Dalgarno pairing used by prokaryotic ribosomes in selection of translation initiators, but for frameshifting the interaction occurs within elongating ribosomes. For dnaX -1 frameshifting, the 3' base of the Shine-Dalgarno sequence is 10 nucleotides 5' of the shift site. Previously, Shine-Dalgarno rRNA-mRNA pairing was shown to stimulate the +1 frameshifting necessary for decoding the release factor 2 gene. However, in the release factor 2 gene, the Shine-Dalgarno sequence is located 3 nucleotides 5' of the shift site. When the Shine-Dalgarno sequence is moved to the same position relative to the dnaX shift site, it is inhibitory rather than stimulatory. Shine-Dalgarno interactions by elongating ribosomes are likely to be used in stimulating -1 frameshifting in the decoding of a variety of genes.
16S rRNA的3'端与mRNA之间的碱基配对对于大肠杆菌dnaX基因解码过程中所利用的程序性-1移码至关重要。这种配对与原核生物核糖体在选择翻译起始位点时所使用的Shine-Dalgarno配对相同,但对于移码而言,这种相互作用发生在正在延伸的核糖体内部。对于dnaX -1移码,Shine-Dalgarno序列的3'碱基位于移码位点5'端10个核苷酸处。此前,已表明Shine-Dalgarno rRNA-mRNA配对可刺激解码释放因子2基因所需的+1移码。然而,在释放因子2基因中,Shine-Dalgarno序列位于移码位点5'端3个核苷酸处。当Shine-Dalgarno序列相对于dnaX移码位点移动到相同位置时,它具有抑制作用而非刺激作用。正在延伸的核糖体的Shine-Dalgarno相互作用可能用于刺激多种基因解码过程中的-1移码。