The protein synthesis inhibitors, oxazolidinones and chloramphenicol, cause extensive translational inaccuracy in vivo

被引:75
作者
Thompson, J
O'Connor, M
Mills, JA
Dahlberg, AE [1 ]
机构
[1] Brown Univ, Dept Mol & Cellular Biol & Biochem, Providence, RI 02912 USA
[2] Essential Therapeut Inc, Mountain View, CA 94043 USA
关键词
translational fidelity; nonsense suppression; frameshifting; antibiotics; ribosomes;
D O I
10.1016/S0022-2836(02)00784-2
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
The oxazolidinone family is a new class of synthetic antibiotics that bind to the bacterial 50 S ribosomal subunit. Two members of the family, linezolid and XA043, were examined for their effects on translational fidelity using a lac Z reporter gene in vivo. Both promoted highly significant frameshifting and nonsense suppression. Chloramphenicol, a peptidyl transferase inhibitor, affected translational fidelity in a similar fashion. Neither the oxazolidinones nor chloramphenicol stimulated misincorporation of amino acid residues at position 461 in the lac Z gene. In contrast, the aminoglycosides gentamicin and paromomycin, which interact with the decoding region of the 30 S subunit, caused significant misincorporation but only modest increases in frameshifting or stop codon readthrough of the lac Z gene. We conclude that effects on translational fidelity may play a significant role in the mechanism of action of the oxazolidinones. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:273 / 279
页数:7
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