Literature DB >> 8941321

The influence of AUG codons in the hepatitis C virus 5' nontranslated region on translation and mapping of the translation initiation window.

R C Rijnbrand1, T E Abbink, P C Haasnoot, W J Spaan, P J Bredenbeek.   

Abstract

The initiation of translation of hepatitis C virus (HCV) is cap-independent and mediated by an internal ribosome entry site (IRES) that is located in the 5' nontranslated region (5' NTR) of the viral genome. This 5' NTR is relatively long and folds into a complex structure involving multiple hairpins and a pseudoknot. Within the sequence encompassing the IRES there are several AUG triplets. Some of these AUG codons are conserved between HCV genotypes and the related pestiviruses. In this study the 5 AUG codons (positions 13, 32, 85, 96, and 215) that are present in the 5' NTR of the HCV H-strain have been mutagenized to determine their influence on HCV cap-independent translation. The effect of these mutations on the expression of a chloramphenicol acetyl transferase (CAT) gene was tested in vaccinia virus. vTF7-3 infected Hep2 cells transfected with plasmids for the expression of a monocistronic HCV 5' NTR-CAT mRNA. Mutating the AUG codons at positions 13, 32, and 215 does not have a significant effect on CAT expression, inactivating the AUG codons at either position 85 or position 96 severely impaired IRES function. To determine whether ribosomes scan the RNA to select the initiation site, AUG codons were inserted up- and downstream of the authentic HCV polyprotein translation initiation codon (position 342). Analysis of these mutants has revealed that the ribosome is unable to use an AUG codon that is placed either 7 nucleotides upstream or 8 nucleotides downstream of the inactivated AUG at position 342. These results indicate that when scanning is involved in the recognition of the translation initiating AUG, it is limited to a narrow region between nucleotides 335 and 350.

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Year:  1996        PMID: 8941321     DOI: 10.1006/viro.1996.0626

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


  26 in total

1.  Inhibition of the protein kinase PKR by the internal ribosome entry site of hepatitis C virus genomic RNA.

Authors:  Jashmin Vyas; Androulla Elia; Michael J Clemens
Journal:  RNA       Date:  2003-07       Impact factor: 4.942

2.  Sendai virus Y proteins are initiated by a ribosomal shunt.

Authors:  P Latorre; D Kolakofsky; J Curran
Journal:  Mol Cell Biol       Date:  1998-09       Impact factor: 4.272

3.  Functional analysis of the interaction between HCV 5'UTR and putative subunits of eukaryotic translation initiation factor eIF3.

Authors:  E Buratti; S Tisminetzky; M Zotti; F E Baralle
Journal:  Nucleic Acids Res       Date:  1998-07-01       Impact factor: 16.971

4.  Gene expression and regulation from the p7 promoter of Aedes densonucleosis virus.

Authors:  M W Kimmick; B N Afanasiev; B J Beaty; J O Carlson
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

5.  A prokaryotic-like mode of cytoplasmic eukaryotic ribosome binding to the initiation codon during internal translation initiation of hepatitis C and classical swine fever virus RNAs.

Authors:  T V Pestova; I N Shatsky; S P Fletcher; R J Jackson; C U Hellen
Journal:  Genes Dev       Date:  1998-01-01       Impact factor: 11.361

6.  Mutational analysis of the GB virus B internal ribosome entry site.

Authors:  R Rijnbrand; G Abell; S M Lemon
Journal:  J Virol       Date:  2000-01       Impact factor: 5.103

7.  Two alternative ways of start site selection in human norovirus reinitiation of translation.

Authors:  Christine Luttermann; Gregor Meyers
Journal:  J Biol Chem       Date:  2014-03-05       Impact factor: 5.157

8.  Specific interaction of eukaryotic translation initiation factor 3 with the 5' nontranslated regions of hepatitis C virus and classical swine fever virus RNAs.

Authors:  D V Sizova; V G Kolupaeva; T V Pestova; I N Shatsky; C U Hellen
Journal:  J Virol       Date:  1998-06       Impact factor: 5.103

9.  A phylogenetically conserved stem-loop structure at the 5' border of the internal ribosome entry site of hepatitis C virus is required for cap-independent viral translation.

Authors:  M Honda; M R Beard; L H Ping; S M Lemon
Journal:  J Virol       Date:  1999-02       Impact factor: 5.103

Review 10.  Structure and functions of hepatitis C virus proteins: 15 years after.

Authors:  L Krekulová; V Rehák; L W Riley
Journal:  Folia Microbiol (Praha)       Date:  2006       Impact factor: 2.099

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