Murine hepatitis virus replicase protein nsp10 is a critical regulator of viral RNA synthesis.

ABSTRACT: Coronavirus replication requires proteolytic processing of the large polyprotein encoded by ORF1a/ab into putative functional intermediates and eventually approximately 15 mature proteins. The C-terminal ORF1a protein nsp10 colocalizes with viral replication complexes, but its role in transcription/replication is not well defined. To investigate the role of nsp10 in coronavirus transcription/replication, alanine replacements were engineered into a murine hepatitis virus (MHV) infectious clone in place of conserved residues in predicted functional domains or charged amino acid pairs/triplets, and rescued viruses were analyzed for mutant phenotypes. Of the 16 engineered clones, 5 viable viruses were rescued, 3 mutant viruses generated no cytopathic effect but were competent to synthesize vir

SUBMITTER: Donaldson EF 

PROVIDER: S-EPMC1900072 | biostudies-literature | 2007 Jun

REPOSITORIES: biostudies-literature