Key result
Arterivirus nsp11 possesses pyrimidine-specific endoribonuclease activity that is independent of divalent cations in vitro, distinguishing its biochemical requirements from coronavirus nsp15.
Arterivirus nsp11 possesses pyrimidine-specific endoribonuclease activity, confirming the nidovirus-wide conservation of this RNA-processing enzyme.
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May guide arterivirus antiviral targeting; confirms nidovirus-wide conservation of cation-independent endoribonuclease activity.
Nidoviruses (arteriviruses, coronaviruses, and roniviruses) are a phylogenetically compact but diverse group of positive-strand RNA viruses that includes important human and animal pathogens. Nidovirus RNA synthesis is mediated by a cytoplasmic membrane-associated replication/transcription complex that includes up to 16 viral nonstructural proteins (nsps), which carry common enzymatic activities, like the viral RNA polymerase, but also unusual and poorly understood RNA-processing functions. Of these, a conserved endoribonuclease (NendoU) is a major genetic marker that is unique to nidoviruses. NendoU activity was previously verified in vitro for the coronavirus nsp15, but not for any of its distantly related orthologs from other nidovirus lineages, like the arterivirus nsp11. Here, we show that the bacterially expressed nsp11 proteins of two arteriviruses, equine arteritis virus and porcine respiratory and reproductive syndrome virus, possess pyrimidine-specific endoribonuclease activity. RNA cleavage was independent of divalent cations in vitro and was greatly reduced by replacement of residues previously implicated in catalysis. Comparative characterization of the NendoU activity in arteriviruses and severe acute respiratory syndrome coronavirus revealed common and distinct features of their substrate requirements and reaction mechanism. Our data provide the first biochemical evidence of endoribonuclease activity associated with arterivirus nsp11 and support the conclusion that this remarkable RNA-processing enzyme, whose substrate in the infected cell remains to be identified, distinguishes nidoviruses from all other RNA viruses.
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Nedialkova et al. (2009) studied this question. Arterivirus nsp11 vs. SARS-CoV nsp15 was evaluated on Endoribonuclease activity and substrate specificity. Arterivirus nsp11 possesses pyrimidine-specific endoribonuclease activity that is independent of divalent cations in vitro, distinguishing its biochemical requirements from coronavirus nsp15.
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