OAS is 2’-5’-oligoadenylate synthetase that, upon activation by dsRNA, catalyzes the synthesis of oligomers of adenylic acid.
These unusual nucleotide oligomers (oligo- (A)) activate RNase L, another IFN stimulated gene, which then begins to degrade viral and cellular mRNAs
The result of all this is an inhibition of viral and cellular protein synthesis and induction of apoptosis.
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2
Q
Virus Mediated Inhibition of OAS/RNase L
A
HIV infection induces the production of an RNase L inhibitor.
Reovirus σ3 protein, Rotavirus nsP3 protein and Influenza A NS1 protein bind dsRNA and inhibit PKR and OAS
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3
Q
MxA Proteins
A
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4
Q
Virus Mediated Inhibition of Mx Proteins
A
Viruses can evade the antiviral effects of Mx proteins through adaptive mutations in their nucleoprotein/capsid protein, which is a key determinant of Mx sensitivity. (e.g. influenza A viruses)
These mutations can allow viruses to overcome the ability of Mx proteins to restrict viral replication.