RIBOSOMAL-RNA-MESSENGER-RNA BASE-PAIRING STIMULATES A PROGRAMMED -1-RIBOSOMAL FRAMESHIFT

被引:114
|
作者
LARSEN, B
WILLS, NM
GESTELAND, RF
ATKINS, JF
机构
[1] UNIV UTAH, DEPT HUMAN GENET, SALT LAKE CITY, UT 84112 USA
[2] UNIV UTAH, HOWARD HUGHES MED INST, SALT LAKE CITY, UT 84112 USA
关键词
D O I
10.1128/JB.176.22.6842-6851.1994
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页码:6842 / 6851
页数:10
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