Cyclic [G(2′,5′) pA(3′,5′)p] Is the Metazoan Second Messenger Produced by DNA-Activated Cyclic GMP-AMP Synthase

被引:812
作者
Gao, Pu [1 ]
Ascano, Manuel [2 ]
Wu, Yang [1 ]
Barchet, Winfried [3 ]
Gaffney, Barbara L. [4 ]
Zillinger, Thomas [3 ]
Serganov, Artem A. [2 ]
Liu, Yizhou [1 ]
Jones, Roger A. [4 ]
Hartmann, Gunther [3 ]
Tuschl, Thomas [2 ]
Patel, Dinshaw J. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Struct Biol Program, New York, NY 10065 USA
[2] Rockefeller Univ, Lab RNA Mol Biol, Howard Hughes Med Inst, New York, NY 10065 USA
[3] Univ Bonn, Univ Hosp Bonn, Inst Clin Chem & Clin Pharmacol, D-53127 Bonn, Germany
[4] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
关键词
C-DI-GMP; STRUCTURAL BASIS; CYTOSOLIC DNA; INTRACELLULAR DNA; I INTERFERON; BACTERIAL; 2ND-MESSENGER; DIGUANYLIC ACID; LIGAND-BINDING; SENSOR; INFLAMMASOME;
D O I
10.1016/j.cell.2013.04.046
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
Recent studies identified cyclic GMP-AMP (cGAMP) as a metazoan second messenger triggering an interferon response. cGAMP is generated from GTP and ATP by cytoplasmic dsDNA sensor cGAMP synthase (cGAS). Wecombined structural, chemical, biochemical, and cellular assays to demonstrate that this second messenger contains G(2',5')pA and A(3',5')pG phosphodiester linkages, designated c[G(2',5') pA(3',5')p]. We show that, upon dsDNA binding, cGAS is activated through conformational transitions, resulting in formation of a catalytically competent and accessible nucleotide-binding pocket for generation of c[G(2',5')pA(3',5')p]. We demonstrate that cyclization occurs in a stepwise manner through initial generation of 5'-pppG(2',5') pA prior to cyclization to c[G(2',5')pA(3',5')p], with the latter positioned precisely in the catalytic pocket. Mutants of cGAS dsDNA-binding or catalytic pocket residues exhibit reduced or abrogated activity. Our studies have identified c[G(2',5')pA(3',5')p] as a founding member of a family of metazoan 2',5'-containing cyclic heterodinucleotide second messengers distinct from bacterial 3',5' cyclic dinucleotides.
引用
收藏
页码:1094 / 1107
页数:14
相关论文
共 37 条
[1]   An orthogonal proteomic-genomic screen identifies AIM2 as a cytoplasmic DNA sensor for the inflammasome [J].
Buerckstuemmer, Tilmann ;
Baumann, Christoph ;
Blueml, Stephan ;
Dixit, Evelyn ;
Duernberger, Gerhard ;
Jahn, Hannah ;
Planyavsky, Melanie ;
Bilban, Martin ;
Colinge, Jacques ;
Bennett, Keiryn L. ;
Superti-Furga, Giulio .
NATURE IMMUNOLOGY, 2009, 10 (03) :266-272
[2]   Structural basis of activity and allosteric control of diguanylate cyclase [J].
Chan, C ;
Paul, R ;
Samoray, D ;
Amiot, NC ;
Giese, B ;
Jenal, U ;
Schirmer, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (49) :17084-17089
[3]   Coordinated Regulation of Accessory Genetic Elements Produces Cyclic Di-Nucleotides for V. cholerae Virulence [J].
Davies, Bryan W. ;
Bogard, Ryan W. ;
Young, Travis S. ;
Mekalanos, John J. .
CELL, 2012, 149 (02) :358-370
[4]   Structural basis for cytosolic double-stranded RNA surveillance by human oligoadenylate synthetase [J].
Donovan, Jesse ;
Dufner, Matthew ;
Korennykh, Alexei .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (05) :1652-1657
[5]   ATOMIC-RESOLUTION STRUCTURE OF THE CELLULOSE SYNTHASE REGULATOR CYCLIC DIGUANYLIC ACID [J].
EGLI, M ;
GESSNER, RV ;
WILLIAMS, LD ;
QUIGLEY, GJ ;
VANDERMAREL, GA ;
VANBOOM, JH ;
RICH, A ;
FREDERICK, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (08) :3235-3239
[6]   AIM2 activates the inflammasome and cell death in response to cytoplasmic DNA [J].
Fernandes-Alnemri, Teresa ;
Yu, Je-Wook ;
Datta, Pinaki ;
Wu, Jianghong ;
Alnemri, Emad S. .
NATURE, 2009, 458 (7237) :509-U5
[7]  
Gaffney B.L., 2012, CURR PROTOC NUCL ACI, V14
[8]   One-Flask Syntheses of c-di-GMP and the [Rp,Rp] and [Rp,Sp] Thiophosphate Analogues [J].
Gaffney, Barbara L. ;
Veliath, Elizabeth ;
Zhao, Jianwei ;
Jones, Roger A. .
ORGANIC LETTERS, 2010, 12 (14) :3269-3271
[9]   Crystal structure of the 2′-specific and double-stranded RNA-activated interferon-induced antiviral protein 2′-5′-oligoadenylate synthetase [J].
Hartmann, R ;
Justesen, J ;
Sarkar, SN ;
Sen, GC ;
Yee, VC .
MOLECULAR CELL, 2003, 12 (05) :1173-1185
[10]   Intracellular DNA recognition [J].
Hornung, Veit ;
Latz, Eicke .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (02) :123-130