Author: Mathew, Suneeth F.; Crowe-McAuliffe, Caillan; Graves, Ryan; Cardno, Tony S.; McKinney, Cushla; Poole, Elizabeth S.; Tate, Warren P.
                    Title: The Highly Conserved Codon following the Slippery Sequence Supports -1 Frameshift Efficiency at the HIV-1 Frameshift Site  Document date: 2015_3_25
                    ID: 10p3mth2_4
                    
                    Snippet: We found previously that the codon immediately following the slippery sequence, that we have termed the intercodon, affects frameshifting mediated by just the slippery sequence in a simple bacterial system [33] . At that time, we proposed a post-translocational mechanism of tRNA slippage from the E and P sites because when the GGG intercodon was changed to a stop codon, frameshift efficiency decreased and was completely eliminated by up-regulatin.....
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: We found previously that the codon immediately following the slippery sequence, that we have termed the intercodon, affects frameshifting mediated by just the slippery sequence in a simple bacterial system [33] . At that time, we proposed a post-translocational mechanism of tRNA slippage from the E and P sites because when the GGG intercodon was changed to a stop codon, frameshift efficiency decreased and was completely eliminated by up-regulating the specific prokaryotic release factor recognising only the cognate stop codon, RF2 [33] . This implied that the intercodon was present in the ribosomal A site prior to frameshifting. Interestingly, stop codons are found at the intercodon position immediately 3´of slippery sequences in several backward frameshift elements, such as those of Rous sarcoma virus and barley yellow dwarf virus [2] , [34] , as well as at the positions of forward frameshifting in +1 PRF elements [4] , [7] .
 
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