4.8 Article

Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells

期刊

ELIFE
卷 3, 期 -, 页码 -

出版社

ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.01535

关键词

-

类别

资金

  1. Cancer Research UK
  2. Medical Research Council
  3. Marie Curie
  4. Fondation Bettencourt-Schueller
  5. European Research Council [AdG-2010-268670]
  6. Netherlands Organisation for Scientific Research [NWO-017.006.043]
  7. Netherlands Organisation for Scientifique Research [NWO-CW-700.59.007]
  8. MRC [MC_UU_12010/8] Funding Source: UKRI
  9. Cancer Research UK [15689] Funding Source: researchfish
  10. Medical Research Council [MC_UU_12010/8] Funding Source: researchfish

向作者/读者索取更多资源

The RIG-I-like receptors RIG-I, LGP2, and MDA5 initiate an antiviral response that includes production of type I interferons (IFNs). The nature of the RNAs that trigger MDA5 activation in infected cells remains unclear. Here, we purify and characterise LGP2/RNA complexes from cells infected with encephalomyocarditis virus (EMCV), a picornavirus detected by MDA5 and LGP2 but not RIG-I. We show that those complexes contain RNA that is highly enriched for MDA5-stimulatory activity and for a specific sequence corresponding to the L region of the EMCV antisense RNA. Synthesis of this sequence by in vitro transcription is sufficient to generate an MDA5 stimulatory RNA. Conversely, genomic deletion of the L region in EMCV generates viruses that are less potent at stimulating MDA5-dependent IFN production. Thus, the L region antisense RNA of EMCV is a key determinant of innate immunity to the virus and represents an RNA that activates MDA5 in virally-infected cells.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据