Ablasser Andrea, Bauernfeind Franz, Hartmann Gunther, Latz Eicke, Fitzgerald Katherine A, Hornung Veit
Institute for Clinical Chemistry and Pharmacology, University of Bonn, Bonn, Germany.
Nat Immunol. 2009 Oct;10(10):1065-72. doi: 10.1038/ni.1779. Epub 2009 Jul 16.
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-kappaB. 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.
RNA可被Toll样受体7(TLR7)和TLR8或RNA解旋酶LGP2、Mda5和RIG-I识别,从而触发抗病毒反应。而关于DNA传感器的了解则少得多。在此,我们鉴定出一种涉及RNA聚合酶III和RIG-I的新型DNA传感途径。在该途径中,富含AT的双链DNA(dsDNA)作为RNA聚合酶III的模板,转录为含有5'-三磷酸基团的双链RNA(dsRNA)。这种dsRNA激活RIG-I会诱导I型干扰素的产生并激活转录因子NF-κB。该途径在识别由RNA聚合酶III转录并随后触发RIG-I激活的爱泼斯坦-巴尔病毒编码的小RNA中起重要作用。因此,RNA聚合酶III和RIG-I在感知病毒DNA方面至关重要。