RIG-I-dependent sensing of poly(dA:dT) through the induction of an RNA polymerase III-transcribed RNA intermediate

被引:696
作者
Ablasser, Andrea [1 ]
Bauernfeind, Franz [1 ]
Hartmann, Gunther [1 ]
Latz, Eicke [2 ]
Fitzgerald, Katherine A. [2 ]
Hornung, Veit [1 ]
机构
[1] Univ Bonn, Inst Clin Chem & Pharmacol, D-5300 Bonn, Germany
[2] Univ Massachusetts, Sch Med, Div Infect Dis & Immunol, Worcester, MA USA
基金
美国国家卫生研究院;
关键词
ANTIVIRAL SIGNALING PROTEIN; INNATE IMMUNE-RESPONSES; EPSTEIN-BARR-VIRUS; NF-KAPPA-B; IFN-BETA; RIBONUCLEIC-ACIDS; ADAPTER PROTEIN; RECOGNITION; DNA; INFLAMMASOME;
D O I
10.1038/ni.1779
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
RNA is sensed by Toll-like receptor 7 (TLR7) and TLR8 or by the RNA helicases LGP2, Mda5 and RIG-I to trigger antiviral responses. Much less is known about sensors for DNA. Here we identify a novel DNA-sensing pathway involving RNA polymerase III and RIG-I. In this pathway, AT-rich double-stranded DNA (dsDNA) served as a template for RNA polymerase III and was transcribed into double-stranded RNA (dsRNA) containing a 5'-triphosphate moiety. Activation of RIG-I by this dsRNA induced production of type I interferon and activation of the transcription factor NF-kappa B. This pathway was important in the sensing of Epstein-Barr virus-encoded small RNAs, which were transcribed by RNA polymerase III and then triggered RIG-I activation. Thus, RNA polymerase III and RIG-I are pivotal in sensing viral DNA.
引用
收藏
页码:1065 / U40
页数:9
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