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Cell Microbiol. 2013 Mar;15(3):386-94. doi: 10.1111/cmi.12061. Epub 2012 Nov 21.

Structural basis of innate immune recognition of viral RNA.

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  • 1Department of Molecular Biophysics & Biochemistry, Yale University, New Haven, CT 06520, USA.

Abstract

Viral RNA is recognized by innate immune receptors from two different families. In endolysosomal compartments, Toll-like receptors (TLRs) 3, 7 and 8 recognize either double-stranded RNA (dsRNA) or single-stranded RNA. In the cytoplasm, viral genomic RNA or transcriptional intermediates are recognized by DExD/H-box helicases RIG-I and MDA5. Recent structural studies of these RNA sensors have provided atomic-level insight into the recognition mechanism of viral RNA. TLR3 dimerizes around a straight 45-bp stretch of dsRNA, explaining the length requirement of at least 40 bp for dsRNA recognition. RIG-I recognizes blunt ends of dsRNA with 5'-triphosphate caps. Ligand binding releases RIG-I from a closed autoinhibited state, exposing the CARD signalling domains. MDA5 recognizes long dsRNA by cooperatively assembling into helical filaments. RNA recognition by RIG-I and MDA5 triggers assembly of their common downstream signalling adaptor MAVS from its inactive monomeric form into its active polymeric form. While RIG-I and MDA5 appear to activate MAVS via distinct oligomerization mechanisms, a common paradigm is emerging in innate immunity for signal transduction by oligomerization-dependent signalling platforms. Many open questions remain including the role of proteolytic activation in RNA recognition by TLR3 and how unanchored ubiquitin chains contribute to RNA recognition by RIG-I and MDA5.

© 2012 Blackwell Publishing Ltd.

PMID:
23110455
[PubMed - indexed for MEDLINE]
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