Table 1.
dsRNA-binding proteins |
dsRNA-binding domains |
Best-known functions | Effect on other dsRNA-binding proteins |
Disease implication |
---|---|---|---|---|
RLRs | Helicase domain, C-terminal domain | Antiviral signal activation | Induce PKR, OASes, and ADARs through interferon signaling | Aicardi-Goutieres syndrome, Singleton-Merten syndrome, systemic lupus erythematosus |
PKR | dsRBDs | Translational suppression | Amplifies RLR signaling | Unknown |
OASes, RNase L | NTase domains | Translational suppression | Amplify RLR signaling | Unknown |
ADARs | dsRBDs | RNA editing and resolving dsRNA structure | Suppress RLRs, PKR, OASes; assist Dicer | Aicardi-Goutieres syndrome |
Dicer, Drosha | PAZ, dsRBDs, RNase III, helicase domain | Processing dsRNAs | Inhibit RLRs | Age-related macular degeneration, polyglutamine diseases |
PACT, TRBP | dsRBDs | Regulate PKR, Dicer, and RLRs | Inhibit PKR, promote Dicer and RLRs | Dystonia |
Helicases (besides RLRs and Dicer) | Helicase domains and others | Regulate dsRNA-dependent immunity | Unknown | Unknown |
Abbreviations: ADAR, adenosine deaminases acting on RNA; dsRBD, dsRNA-binding domain; NTase, nucleotide transferase; OASes, oligoadenylate synthases; PAZ, Piwi Argonaute and Zwille; PKR, protein kinase R; RLR, RIG-I-like receptor; RNase, ribonuclease.