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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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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
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author Brayton, Peter R.
Stohlman, Stephen A.
Lai, Michael M.C.
author_facet Brayton, Peter R.
Stohlman, Stephen A.
Lai, Michael M.C.
author_sort Brayton, Peter R.
collection PubMed
description 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.
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spelling pubmed-71306202020-04-08 Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases Brayton, Peter R. Stohlman, Stephen A. Lai, Michael M.C. Virology Article 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. Published by Elsevier Inc. 1984-02 2004-06-09 /pmc/articles/PMC7130620/ /pubmed/6322429 http://dx.doi.org/10.1016/0042-6822(84)90439-2 Text en Copyright © 1984 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Brayton, Peter R.
Stohlman, Stephen A.
Lai, Michael M.C.
Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases
title Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases
title_full Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases
title_fullStr Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases
title_full_unstemmed Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases
title_short Further characterization of mouse hepatitis virus RNA-dependent RNA polymerases
title_sort further characterization of mouse hepatitis virus rna-dependent rna polymerases
topic Article
url 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
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