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Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases

Two temporally and enzymatically distinct RNA-dependent RNA polymerase activities associated with membranes of the mouse hepatitis virus (MHV)-infected cells have been identified previously [Brayton et al., J. Virol.42, 847–853 (1982)]. In this paper, the subcellular distribution and functions of th...

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Detalles Bibliográficos
Autores principales: Brayton, Peter R., Stohlman, Stephen A., Lai, Michael M.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7130620/
https://www.ncbi.nlm.nih.gov/pubmed/6322429
http://dx.doi.org/10.1016/0042-6822(84)90439-2
Descripción
Sumario:Two temporally and enzymatically distinct RNA-dependent RNA polymerase activities associated with membranes of the mouse hepatitis virus (MHV)-infected cells have been identified previously [Brayton et al., J. Virol.42, 847–853 (1982)]. In this paper, the subcellular distribution and functions of these two polymerases were examined. Fractionation of the postnuclear membranes by sucrose gradient sedimentation showed that the early polymerase activity (detected at 1 hr p.i.) was homogeneous, while the late polymeras e (6 hr p.i.) was associated with two distinct membrane fractions. The early polymerase synthesized a single RNA species of viral genomic size and negative sense. In contrast, the light peak of the late polymerase synthesized genomic-sized RNA of positive sense, while the heavy peak of the activity synthesized positive-sensed genomic and subgenomic mRNAs. These findings suggest that the light peak of the late polymerase represents a replication complex while the heavy peak represents a transcription complex. They also establish the essential features of the mode of replication of MHV.