Innate immunity induced by composition-dependent RIG-I recognition of hepatitis C virus RNA
By Takeshi Saito, D. Owen, F. Jiang, J. Marcotrigiano, M. Gale. Nature, 2008
787 citations recorded by the source corpus.
Subfields: Epidemiology, Hepatology, Immunology
View Paper: https://www.semanticscholar.org/paper/15cb7ce0a9b033208be6ecfc0e149dbf1f8f0947
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Citations in the corpus
- Preference of RIG-I for short viral RNA molecules in infected cells revealed by next-generation sequencing (2010, background): “Additionally, 5′ppp containing RNAs rich in U residues have been found to act as more potent inducers of RIG-I, indicating that sequence composition might play a role in activation (22).”
- Structural Basis of RNA Recognition and Activation by Innate Immune Receptor RIG-I (2011, methodology): “The observed fluorescence anisotropy (robs) as a function of protein concentration (Pt) was fit to equations (1) and (2) to obtain the equilibrium dissociation constant, Kd.”
- RNA recognition and signal transduction by RIG‐I‐like receptors (2009, background): “It should be noted that a recent report suggested that RIG-I requires a polyuridine motif at the 3¢-non-translated region of the HCV genome; however, it remains to be addressed whether this is the case for other viruses (63).”
- 5′-triphosphate RNA requires base-paired structures to activate antiviral signaling via RIG-I (2009, background): “Recently, it was suggested that viral RNA requires A- or U-rich stretches to activate RIG-I (15).”
- Viral evasion and subversion of pattern-recognition receptor signalling (2008, background): “Although the 5′ triphosphate is necessary, it is not sufficient for RIG-I activatio”
- RIG-I detects viral genomic RNA during negative-strand RNA virus infection. (2010, background): “, 2008) and, in some cases, to require specific structural determinants or sequence motifs (Marques et al., 2006; Saito et al., 2008; Schlee et al., 2009b; Schmidt et al., 2009; Uzri and Gehrke, 2009).”
- Pattern recognition receptors and inflammation. (2010, methodology): “Poly(U)- or poly(A)-rich sequences from the HCV RNA 30 untranslated region (UTR) are responsible for RIG-I-mediated IFN production, based on RNAs generated by in vitro transcription using T7 polymerase (Saito et al., 2008).”