Recognition of the bacterial second messenger cyclic diguanylate by its cognate riboswitch

被引:159
作者
Kulshina, Nadia [1 ,3 ]
Baird, Nathan J. [2 ,3 ]
Ferre-D'Amare, Adrian R. [1 ,2 ,3 ]
机构
[1] Univ Washington, Mol & Cellular Biol Program, Seattle, WA 98195 USA
[2] Fred Hutchinson Canc Res Ctr, Howard Hughes Med Inst, Seattle, WA 98104 USA
[3] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
基金
美国国家卫生研究院;
关键词
CRYSTAL-STRUCTURES; STRUCTURAL BASIS; BIOLOGICAL MACROMOLECULES; SOLUTION SCATTERING; LIGAND-BINDING; RNA; GUANINE; RIBOZYME; RESOLUTION; CRYSTALLIZATION;
D O I
10.1038/nsmb.1701
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 cyclic diguanylate (bis-(3'-5')-cyclic dimeric guanosine monophosphate, c-di-GMP) riboswitch is the first known example of a gene-regulatory RNA that binds a second messenger. c-di-GMP is widely used by bacteria to regulate processes ranging from biofilm formation to the expression of virulence genes. The cocrystal structure of the c-di-GMP responsive GEMM riboswitch upstream of the tfoX gene of Vibrio cholerae reveals the second messenger binding the RNA at a three-helix junction. The two-fold symmetric second messenger is recognized asymmetrically by the monomeric riboswitch using canonical and noncanonical base-pairing as well as intercalation. These interactions explain how the RNA discriminates against cyclic diadenylate (c-di-AMP), a putative bacterial second messenger. Small-angle X-ray scattering and biochemical analyses indicate that the RNA undergoes compaction and large-scale structural rearrangement in response to ligand binding, consistent with organization of the core three-helix junction of the riboswitch concomitant with binding of c-di-GMP.
引用
收藏
页码:1212 / 1217
页数:7
相关论文
共 56 条
[1]   Structure of a folding intermediate reveals the interplay between core and peripheral elements in RNA folding [J].
Baird, NJ ;
Westhof, E ;
Qin, H ;
Pan, T ;
Sosnick, TR .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 352 (03) :712-722
[2]   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
[3]   Crystallography & NMR system:: A new software suite for macromolecular structure determination [J].
Brunger, AT ;
Adams, PD ;
Clore, GM ;
DeLano, WL ;
Gros, P ;
Grosse-Kunstleve, RW ;
Jiang, JS ;
Kuszewski, J ;
Nilges, M ;
Pannu, NS ;
Read, RJ ;
Rice, LM ;
Simonson, T ;
Warren, GL .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1998, 54 :905-921
[4]   Ribbons [J].
Carson, M .
MACROMOLECULAR CRYSTALLOGRAPHY, PT B, 1997, 277 :493-505
[5]   Mechanism of mRNA destabilization by the glmS ribozyme [J].
Collins, Jennifer A. ;
Irnov, Irnov ;
Baker, Stephanie ;
Winkler, Wade C. .
GENES & DEVELOPMENT, 2007, 21 (24) :3356-3368
[6]   THE CONTACTS OF YEAST TRANSFER RNASER WITH SERYL-TRANSFER RNA-SYNTHETASE STUDIED BY FOOTPRINTING EXPERIMENTS [J].
DOCKBREGEON, AC ;
GARCIA, A ;
GIEGE, R ;
MORAS, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 188 (02) :283-290
[7]   Riboswitches:: small-molecule recognition by gene regulatory RNAs [J].
Edwards, Thomas E. ;
Klein, Daniel J. ;
Ferre-D'Amare, Adrian R. .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2007, 17 (03) :273-279
[8]   Crystal structures of the thi-box riboswitch bound to thiamine pyrophosphate analogs reveal adaptive RNA-small molecule recognition [J].
Edwards, Thomas E. ;
Ferre-D'Amare, Adrian R. .
STRUCTURE, 2006, 14 (09) :1459-1468
[9]   PROBING THE STRUCTURE OF RNAS IN SOLUTION [J].
EHRESMANN, C ;
BAUDIN, F ;
MOUGEL, M ;
ROMBY, P ;
EBEL, JP ;
EHRESMANN, B .
NUCLEIC ACIDS RESEARCH, 1987, 15 (22) :9109-9128
[10]   Footprinting analysis demonstrates extensive similarity between eukaryotic RNase P and RNase MRP holoenzymes [J].
Esakova, Olga ;
Perederina, Anna ;
Quan, Chao ;
Schmitt, Mark E. ;
Krasilnikov, Andrey S. .
RNA, 2008, 14 (08) :1558-1567