Inhibitory activity for the interferon-induced protein kinase is associated with the reovirus serotype 1 σ3 protein

F. Imani, Bertram Jacobs

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Abstract

In this report we demonstrate that reovirus serotype 1-infected cells contain an inhibitor of the interferon-induced, double-stranded RNA (dsRNA)-dependent protein kinase. We provide evidence that suggests that the virus-encoded σ3 protein is likely responsible for this kinase inhibitory activity. We could not detect activation of the dsRNA-dependent protein kinase in extracts prepared from either interferon-treated or untreated reovirus serotype 1-infected mouse L cells under conditions that led to activation of the kinase in extracts prepared from either interferon-treated or untreated, uninfected cells. Extracts from reovirus-infected cells blocked activation of kinase in extracts from interferon-treated cells when the two were mixed prior to assay. The kinase inhibitory activity in extracts of reovirus-infected cells could be overcome by adding ~100-fold excess of dsRNA over the amount required to activate kinase in extracts of uninfected cells. Kinase inhibitory activity in extracts of interferon-treated, virus-infected cells could be overcome with somewhat less dsRNA (~10-fold excess). Most of the inhibitory activity in the extracts could be removed by adsorption with immobilized anti-reovirus σ3 serum or immobilized dsRNA, suggesting that the dsRNA-binding σ3 protein is necessary for kinase inhibitory activity. Purified σ3 protein, when added to reaction mixtures containing partially purified kinase, inhibited enzyme activation. Control of activation of this kinase, which can modify eukaryotic protein synthesis initiation factor 2, may be relevant to the sensitivity of reovirus replication to treatment of cells with interferon and to the shutoff of host protein synthesis in reovirus-infected cells.

Original languageEnglish (US)
Pages (from-to)7887-7891
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume85
Issue number21
DOIs
StatePublished - Jan 1 1988

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