Effect of mutations in the A site of 16S rRNA on aminoglycoside antibiotic-ribosome interaction

被引:85
作者
Recht, MI
Douthwaite, S
Dahlquist, KD
Puglisi, JD [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Struct Biol, Stanford, CA 94305 USA
[2] Odense Univ, Dept Mol Biol, DK-5320 Odense M, Denmark
关键词
decoding region; paromomycin; rRNA structure; antibiotic resistance;
D O I
10.1006/jmbi.1998.2446
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Decoding of genetic information occurs upon interaction of an mRNA codon-tRNA anticodon complex with the small subunit of the ribosome. The ribosomal decoding region is associated with highly conserved sequences near the 3' end of 16 S rRNA. The decoding process is perturbed by the aminoglycoside antibiotics, which also interact with this region of rRNA. Mutations of certain nucleotides in rRNA reduce aminoglycoside binding affinity, as previously demonstrated using a model RNA oligonucleotide system. Here, predictions from the oligonucleotide system were tested in the ribosome by mutation of universally conserved nucleotides at 1406 to 1408 and 1494 to 1495 in the decoding region of plasmid-encoded bacterial 16 S rRNA. Phenotypic changes range from the benign effect of U1406 --> A or A1408 --> G substitutions, to the highly deleterious 1406G and 1495 mutations that assemble into 30 S subunits but are defective in forming functional ribosomes. Changes in the local conformation of the decoding region caused by these mutations were identified by chemical probing of isolated 30 S subunits. Ribosomes containing 16 S rRNA with mutations at positions 1408, 1407 + 1494, or 1495 had reduced affinity for the aminoglycoside paromomycin, whereas no discernible reduction in affinity was observed with 1406 mutant ribosomes. These data are consistentwith prior NMR structural determination of aminoglycoside interaction with the decoding region, and further our understanding of how aminoglycoside resistance can be conferred. (C) 1999 Academic Press.
引用
收藏
页码:33 / 43
页数:11
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