scholarly journals The Effect of L3T4 T Cell Depletion on the Pathogenesis of Theiler's Murine Encephalomyelitis Virus Infection in CBA Mice

1987 ◽  
Vol 68 (6) ◽  
pp. 1659-1667 ◽  
Author(s):  
C. J. R. Welsh ◽  
P. Tonks ◽  
A. A. Nash ◽  
W. F. Blakemore
2019 ◽  
Vol 47 (15) ◽  
pp. 8207-8223 ◽  
Author(s):  
Sawsan Napthine ◽  
Susanne Bell ◽  
Chris H Hill ◽  
Ian Brierley ◽  
Andrew E Firth

AbstractMany viruses utilize programmed –1 ribosomal frameshifting (–1 PRF) to express additional proteins or to produce frameshift and non-frameshift protein products at a fixed stoichiometric ratio. PRF is also utilized in the expression of a small number of cellular genes. Frameshifting is typically stimulated by signals contained within the mRNA: a ‘slippery’ sequence and a 3′-adjacent RNA structure. Recently, we showed that −1 PRF in encephalomyocarditis virus (EMCV) is trans-activated by the viral 2A protein, leading to a temporal change in PRF efficiency from 0% to 70% during virus infection. Here we analyzed PRF in the related Theiler's murine encephalomyelitis virus (TMEV). We show that 2A is also required for PRF in TMEV and can stimulate PRF to levels as high as 58% in rabbit reticulocyte cell-free translations and 81% during virus infection. We also show that TMEV 2A trans-activates PRF on the EMCV signal but not vice versa. We present an extensive mutational analysis of the frameshift stimulators (mRNA signals and 2A protein) analysing activity in in vitro translation, electrophoretic mobility shift and in vitro ribosome pausing assays. We also investigate the PRF mRNA signal with RNA structure probing. Our results substantially extend previous characterization of protein-stimulated PRF.


2015 ◽  
Vol 593 ◽  
pp. 124-128 ◽  
Author(s):  
Ellen Merckx ◽  
Thomas Demuyser ◽  
Eduard Bentea ◽  
Joeri Van Liefferinge ◽  
Giulia Albertini ◽  
...  

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