Literature DB >> 8395114

Evidence for new transcriptional units encoded at the 3' end of the mouse hepatitis virus genome.

M C Schaad1, R S Baric.   

Abstract

Prior studies have demonstrated that the mouse hepatitis virus (MHV) genome is divided into at least seven coding regions each transcribed into a distinct mRNA. The majority of these mRNAs are synthesized from a highly conserved intergenic start site (UCU/CAAAC), contain a 65-72 nt leader RNA at their 5' end and form a 3' co-terminal nested set. In this study, we have used radiolabeling experiments to demonstrate the presence of a small approximately 900 nt mRNA and its corresponding RF RNA in MHV-infected cells. Surprisingly, PCR amplification and sequence analysis revealed the presence of not one, but two small leader-containing RNAs that initiate from highly conserved intergenic start sites (UCCAAAC and UCUAAAU) which are located within the 3'-most nucleocapsid gene sequence. These studies provide evidence suggesting that one or two additional small mRNAs are encoded from the 3' end of the MHV genome.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8395114     DOI: 10.1006/viro.1993.1467

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  15 in total

1.  Secondary structure and function of the 5'-proximal region of the equine arteritis virus RNA genome.

Authors:  Erwin Van Den Born; Alexander P Gultyaev; Eric J Snijder
Journal:  RNA       Date:  2004-03       Impact factor: 4.942

2.  Coronaviruses as vectors: stability of foreign gene expression.

Authors:  Cornelis A M de Haan; Bert Jan Haijema; David Boss; Frank W H Heuts; Peter J M Rottier
Journal:  J Virol       Date:  2005-10       Impact factor: 5.103

3.  Analysis of a recombinant mouse hepatitis virus expressing a foreign gene reveals a novel aspect of coronavirus transcription.

Authors:  F Fischer; C F Stegen; C A Koetzner; P S Masters
Journal:  J Virol       Date:  1997-07       Impact factor: 5.103

4.  Expanded subgenomic mRNA transcriptome and coding capacity of a nidovirus.

Authors:  Han Di; Joseph C Madden; Esther K Morantz; Hsin-Yao Tang; Rachel L Graham; Ralph S Baric; Margo A Brinton
Journal:  Proc Natl Acad Sci U S A       Date:  2017-10-04       Impact factor: 11.205

5.  Function of a 5'-end genomic RNA mutation that evolves during persistent mouse hepatitis virus infection in vitro.

Authors:  W Chen; R S Baric
Journal:  J Virol       Date:  1995-12       Impact factor: 5.103

6.  Genetics of mouse hepatitis virus transcription: evidence that subgenomic negative strands are functional templates.

Authors:  M C Schaad; R S Baric
Journal:  J Virol       Date:  1994-12       Impact factor: 5.103

7.  Molecular anatomy of mouse hepatitis virus persistence: coevolution of increased host cell resistance and virus virulence.

Authors:  W Chen; R S Baric
Journal:  J Virol       Date:  1996-06       Impact factor: 5.103

8.  Reverse genetic analysis of the transcription regulatory sequence of the coronavirus transmissible gastroenteritis virus.

Authors:  Kristopher M Curtis; Boyd Yount; Amy C Sims; Ralph S Baric
Journal:  J Virol       Date:  2004-06       Impact factor: 5.103

9.  Map locations of mouse hepatitis virus temperature-sensitive mutants: confirmation of variable rates of recombination.

Authors:  K Fu; R S Baric
Journal:  J Virol       Date:  1994-11       Impact factor: 5.103

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

Authors:  Eric F Donaldson; Amy C Sims; Rachel L Graham; Mark R Denison; Ralph S Baric
Journal:  J Virol       Date:  2007-03-28       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.