Riboswitches as antibacterial drug targets

被引:346
作者
Blount, Kenneth F.
Breaker, Ronald R.
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[3] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
D O I
10.1038/nbt1268
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
New validated cellular targets are needed to reinvigorate antibacterial drug discovery. This need could potentially be filled by riboswitches - messenger RNA ( mRNA) structures that regulate gene expression in bacteria. Riboswitches are unique among RNAs that serve as drug targets in that they have evolved to form structured and highly selective receptors for small drug-like metabolites. In most cases, metabolite binding to the receptor represses the expression of the gene( s) encoded by the mRNA. If a new metabolite analog were designed that binds to the receptor, the gene( s) regulated by that riboswitch could be repressed, with a potentially lethal effect to the bacteria. Recent work suggests that certain antibacterial compounds discovered decades ago function at least in part by targeting riboswitches. Herein we will summarize the experiments validating riboswitches as drug targets, describe the existing technology for riboswitch drug discovery and discuss the challenges that may face riboswitch drug discoverers.
引用
收藏
页码:1558 / 1564
页数:7
相关论文
共 63 条
[1]   Biosynthesis of vitamin B2 (riboflavin) [J].
Bacher, A ;
Eberhardt, S ;
Fischer, M ;
Kis, K ;
Richter, G .
ANNUAL REVIEW OF NUTRITION, 2000, 20 :153-167
[2]   New RNA motifs suggest an expanded scope for riboswitches in bacterial genetic control [J].
Barrick, JE ;
Corbino, KA ;
Winkler, WC ;
Nahvi, A ;
Mandal, M ;
Collins, J ;
Lee, M ;
Roth, A ;
Sudarsan, N ;
Jona, I ;
Wickiser, JK ;
Breaker, RR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (17) :6421-6426
[3]   Structure of a natural guanine-responsive riboswitch complexed with the metabolite hypoxanthine [J].
Batey, RT ;
Gilbert, SD ;
Montange, RK .
NATURE, 2004, 432 (7015) :411-415
[4]  
BEREZOVSKII VM, 1977, BIOORG KHIM+, V3, P521
[5]  
Blount Kenneth, 2006, RNA Biol, V3, P77
[6]  
BLOUNT KF, 2007, IN PRESS NAT CHEM BI
[7]   Riboflavin production in Lactococcus lactis:: Potential for in situ production of vitamin-enriched foods [J].
Burgess, C ;
O'Connell-Motherway, M ;
Sybesma, W ;
Hugenholtz, J ;
van Sinderen, D .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) :5769-5777
[8]   Evidence for a second class of S-adenosylmethionine riboswitches and other regulatory RNA motifs in alpha-proteobacteria -: art. no. r70 [J].
Corbino, KA ;
Barrick, JE ;
Lim, J ;
Welz, R ;
Tucker, BJ ;
Puskarz, I ;
Mandal, M ;
Rudnick, ND ;
Breaker, RR .
GENOME BIOLOGY, 2005, 6 (08)
[9]   Sampling the antibiotic resistome [J].
D'Costa, VM ;
McGrann, KM ;
Hughes, DW ;
Wright, GD .
SCIENCE, 2006, 311 (5759) :374-377
[10]  
DIGIROLAMO M, 1986, PHYSIOL CHEM PHYS M, V18, P159