Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783517051578482688 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7130620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1984 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT braytonpeterr furthercharacterizationofmousehepatitisvirusrnadependentrnapolymerases AT stohlmanstephena furthercharacterizationofmousehepatitisvirusrnadependentrnapolymerases AT laimichaelmc furthercharacterizationofmousehepatitisvirusrnadependentrnapolymerases |