NONCOMPETITIVE INHIBITION OF GROUP-I INTRON RNA SELF-SPLICING BY AMINOGLYCOSIDE ANTIBIOTICS

被引:116
作者
VONAHSEN, U
DAVIES, J
SCHROEDER, R
机构
[1] UNIV VIENNA, INST MIKROBIOL & GENET, A-1090 VIENNA, AUSTRIA
[2] UNIV BRITISH COLUMBIA, DEPT MICROBIOL, VANCOUVER V6T 1Z3, BC, CANADA
基金
奥地利科学基金会;
关键词
AUTOCATALYTIC RNA; 2-DEOXYSTREPTAMINE; RIBOZYME; RIBOSOME;
D O I
10.1016/0022-2836(92)91043-O
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
Aminoglycoside antibiotics inhibit self-splicing of group I intron RNA in vitro at concentrations as low as 10-6 m. The sites of interaction and the mechanism of inhibition have yet to be determined. A comparative study of inhibition by different 2-deoxystreptamine analogues reveals structural features of the aminoglycoside antibiotics required for their interaction and effect on group I introns. Complete antibiotic inhibition of the two steps of splicing was not reversed at high concentrations of guanosine, indicating a non-competitive inhibition. A mutant group I intron in which the conserved guanosine nucleotide of the G-binding site had been replaced by an adenosine, was sensitive to the antibiotics providing direct evidence that the antibiotics do not interact with the G-binding site in the same way as the guanine base. In addition kinetic analyses of the self-splicing process in the presence of antibiotic inhibitors supported a non-competitive mechanism of the mixed type for inhibition of the ribozyme. © 1992.
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页码:935 / 941
页数:7
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