Structural basis for discriminative regulation of gene expression by adenine- and guanine-sensing mRNAs

被引:443
作者
Serganov, A
Yuan, YR
Pikovskaya, O
Polonskaia, A
Malinina, L
Phan, AT
Hobartner, C
Micura, R
Breaker, RR
Patel, DJ
机构
[1] Mem Sloan Kettering Canc Ctr, Struct Biol Program, New York, NY 10021 USA
[2] Leopold Franzens Univ, Ctr Mol Biosci, Inst Organ Chem, A-6020 Innsbruck, Austria
[3] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
来源
CHEMISTRY & BIOLOGY | 2004年 / 11卷 / 12期
关键词
D O I
10.1016/j.chembiol.2004.11.018
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
Metabolite-sensing mRNAs, or "riboswitches," specifically interact with small ligands and direct expression of the genes involved in their metabolism. Riboswitches contain sensing "aptamer" modules, capable of ligand-induced structural changes, and downstream regions, harboring expression-controlling elements. We report the crystal structures of the add A-riboswitch and xpt G-riboswitch aptamer modules that distinguish between bound adenine and guanine with exquisite specificity and modulate expression of two different sets of genes. The riboswitches form tuning fork-like architectures, in which the prongs are held in parallel through hairpin loop interactions, and the internal bubble zippers up to form the purine binding pocket. The bound purines are held by hydrogen bonding interactions involving conserved nucleotides along their entire periphery. Recognition specificity is associated with Watson-Crick pairing of the encapsulated adenine and guanine ligands with uridine and cytosine, respectively.
引用
收藏
页码:1729 / 1741
页数:13
相关论文
共 53 条
[1]   Methods used in the structure determination of bovine mitochondrial F-1 ATPase [J].
Abrahams, JP ;
Leslie, AGW .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1996, 52 :30-42
[2]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[3]   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
[4]  
Batey RT, 1999, ANGEW CHEM INT EDIT, V38, P2327
[5]   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
[6]   Specificity of RNA-RNA helix recognition [J].
Battle, DJ ;
Doudna, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (18) :11676-11681
[7]   Engineered allosteric ribozymes as biosensor components [J].
Breaker, RR .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (01) :31-39
[8]  
Brunger AT, 1998, ACTA CRYSTALLOGR D, V54, P905, DOI 10.1107/s0907444998003254
[9]  
CATE JH, 1996, SCIENCE, V20, P1696
[10]   Maximum-likelihood heavy-atom parameter refinement for multiple isomorphous replacement and multiwavelength anomalous diffraction methods [J].
delaFortelle, E ;
Bricogne, G .
MACROMOLECULAR CRYSTALLOGRAPHY, PT A, 1997, 276 :472-494