Double-Stranded RNA Sensors and Modulators in Innate Immunity

被引:274
作者
Hur, Sun [1 ,2 ]
机构
[1] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 37, 2019 | 2019年 / 37卷
关键词
dsRNA; RIG-I-like receptor; protein kinase R; oligoadenylate synthase; dsRNA-dependent adenosine deaminase; RNA interference; PROTEIN-KINASE PKR; 2'-5' OLIGOADENYLATE SYNTHETASE; RIG-I; BINDING-PROTEIN; ADENOSINE-DEAMINASE; STRUCTURAL BASIS; DSRNA BINDING; TAR-RNA; INDUCED ACTIVATION; ANTIVIRAL ACTIVITY;
D O I
10.1146/annurev-immunol-042718-041356
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Detection of double-stranded RNAs (dsRNAs) is a central mechanism of innate immune defense in many organisms. We here discuss several families of dsRNA-binding proteins involved in mammalian antiviral innate immunity. These include RIG-I-like receptors, protein kinase R, oligoadenylate synthases, adenosine deaminases acting on RNA, RNA interference systems, and other proteins containing dsRNA-binding domains and helicase domains. Studies suggest that their functions are highly interdependent and that their interdependence could offer keys to understanding the complex regulatory mechanisms for cellular dsRNA homeostasis and antiviral immunity. This review aims to highlight their interconnectivity, as well as their commonalities and differences in their dsRNA recognition mechanisms.
引用
收藏
页码:349 / 375
页数:27
相关论文
共 217 条
[91]   The Oligoadenylate Synthetase Family: An Ancient Protein Family with Multiple Antiviral Activities [J].
Kristiansen, Helle ;
Gad, Hans Henrik ;
Eskildsen-Larsen, Signe ;
Despres, Philippe ;
Hartmann, Rune .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2011, 31 (01) :41-47
[92]   Structure of Human DROSHA [J].
Kwon, S. Chul ;
Tuan Anh Nguyen ;
Choi, Yeon-Gil ;
Jo, Myung Hyun ;
Hohng, Sungchul ;
Kim, V. Narry ;
Woo, Jae-Sung .
CELL, 2016, 164 (1-2) :81-90
[93]   MDA5 Localizes to Stress Granules, but This Localization Is Not Required for the Induction of Type I Interferon [J].
Langereis, Martijn A. ;
Feng, Qian ;
van Kuppeveld, Frank J. .
JOURNAL OF VIROLOGY, 2013, 87 (11) :6314-6325
[94]   Interactions between the double-stranded RNA-binding proteins TRBP and PACT define the Medipal domain that mediates protein-protein interactions [J].
Laraki, Ghislaine ;
Clerzius, Guerline ;
Daher, Aicha ;
Melendez-Pena, Carlos ;
Daniels, Sylvanne ;
Gatignol, Anne .
RNA BIOLOGY, 2008, 5 (02) :92-103
[95]   Emerging roles of DROSHA beyond primary microRNA processing [J].
Lee, Dooyoung ;
Shin, Chanseok .
RNA BIOLOGY, 2018, 15 (02) :186-193
[96]   Differential roles of human Dicer-binding proteins TRBP and PACT in small RNA processing [J].
Lee, Ho Young ;
Zhou, Kaihong ;
Smith, Alison Marie ;
Noland, Cameron L. ;
Doudna, Jennifer A. .
NUCLEIC ACIDS RESEARCH, 2013, 41 (13) :6568-6576
[97]   OASL1 inhibits translation of the type I interferon-regulating transcription factor IRF7 [J].
Lee, Myeong Sup ;
Kim, Byungil ;
Oh, Goo Taeg ;
Kim, Young-Joon .
NATURE IMMUNOLOGY, 2013, 14 (04) :346-355
[98]   The biology of DHX9 and its potential as a therapeutic target [J].
Lee, Teresa ;
Pelletier, Jerry .
ONCOTARGET, 2016, 7 (27) :42716-42739
[99]   The role of PACT in the RNA silencing pathway [J].
Lee, Y ;
Hur, I ;
Park, SY ;
Kim, YK ;
Suh, MR ;
Kim, VN .
EMBO JOURNAL, 2006, 25 (03) :522-532
[100]   Structure of the kinase domain of human RNA-dependent protein kinase with K296R mutation reveals a face-to-face dimer [J].
Li FengZhi ;
Li SiWei ;
Wang Zheng ;
Shen YueQuan ;
Zhang TongCun ;
Yang Xue .
CHINESE SCIENCE BULLETIN, 2013, 58 (09) :998-1002