Literature DB >> 6296295

RNA-dependent RNA polymerase activity in murine coronavirus-infected cells.

B W Mahy, S Siddell, H Wege, V ter Meulen.   

Abstract

The multiplication of murine coronavirus strains A59 or JHM in Sac(-) cells was unaffected by the presence of alpha-amanitin at concentrations which inhibited the host cell DNA-dependent RNA polymerase activity. In cells infected with the A59 virus strain, actinomycin D-resistant RNA synthesis could readily be detected by pulse-labelling with [3H]uridine; this virus-specific RNA synthesis was not induced in the presence of the protein synthesis inhibitor anisomycin. A new RNA-dependent RNA polymerase activity was detected in the large particle fraction of A59 virus-infected cells. Optimal conditions for enzyme activity in vitro were established. Maximum activity occurred 5 h after infection, coincident with the peak of virus-specific RNA synthesis detected by pulse-labelling in vivo.

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Year:  1983        PMID: 6296295     DOI: 10.1099/0022-1317-64-1-103

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  24 in total

1.  Characterization of coronavirus RNA polymerase gene products.

Authors:  J Herold; S Siddell; J Ziebuhr
Journal:  Methods Enzymol       Date:  1996       Impact factor: 1.600

2.  Coronavirus genomic and subgenomic minus-strand RNAs copartition in membrane-protected replication complexes.

Authors:  P B Sethna; D A Brian
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

3.  Structure of the intracellular defective viral RNAs of defective interfering particles of mouse hepatitis virus.

Authors:  S Makino; N Fujioka; K Fujiwara
Journal:  J Virol       Date:  1985-05       Impact factor: 5.103

4.  Mechanism of coronavirus transcription: duration of primary transcription initiation activity and effects of subgenomic RNA transcription on RNA replication.

Authors:  Y S Jeong; S Makino
Journal:  J Virol       Date:  1992-06       Impact factor: 5.103

5.  Colocalization and membrane association of murine hepatitis virus gene 1 products and De novo-synthesized viral RNA in infected cells.

Authors:  S T Shi; J J Schiller; A Kanjanahaluethai; S C Baker; J W Oh; M M Lai
Journal:  J Virol       Date:  1999-07       Impact factor: 5.103

6.  In vitro replication of mouse hepatitis virus strain A59.

Authors:  S R Compton; D B Rogers; K V Holmes; D Fertsch; J Remenick; J J McGowan
Journal:  J Virol       Date:  1987-06       Impact factor: 5.103

7.  The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanism.

Authors:  P J Bredenbeek; C J Pachuk; A F Noten; J Charité; W Luytjes; S R Weiss; W J Spaan
Journal:  Nucleic Acids Res       Date:  1990-04-11       Impact factor: 16.971

8.  Coronavirus mRNA synthesis involves fusion of non-contiguous sequences.

Authors:  W Spaan; H Delius; M Skinner; J Armstrong; P Rottier; S Smeekens; B A van der Zeijst; S G Siddell
Journal:  EMBO J       Date:  1983       Impact factor: 11.598

9.  SARS-coronavirus replication/transcription complexes are membrane-protected and need a host factor for activity in vitro.

Authors:  Martijn J van Hemert; Sjoerd H E van den Worm; Kèvin Knoops; A Mieke Mommaas; Alexander E Gorbalenya; Eric J Snijder
Journal:  PLoS Pathog       Date:  2008-05-02       Impact factor: 6.823

10.  Defective-interfering particles of murine coronavirus: mechanism of synthesis of defective viral RNAs.

Authors:  S Makino; C K Shieh; J G Keck; M M Lai
Journal:  Virology       Date:  1988-03       Impact factor: 3.616

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