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pUC57 plasmid DNA> | ...tRNAHis (CAC) were made by inserting DNA sequences flanked by a T7 promoter and a BstN1 restriction site into pUC57 (<b>GenScript</b> Corporation), and for 5U mRNA was made by inserting DNA flanked by a T7 promoter between PstI and SmaI restriction sites of pUC18 (Picoscript)... | Get A Quote |
After translational termination, mRNA and P site deacylated tRNA remain associated with ribosomes in posttermination complexes (post-TCs), which must therefore be recycled by releasing mRNA and deacylated tRNA and by dissociating ribosomes into subunits. Recycling of bacterial post-TCs requires elongation factor EF-G and a ribosome recycling factor RRF. Eukaryotes do not encode a RRF homolog, and their mechanism of ribosomal recycling is unknown. We investigated eukaryotic recycling using post-TCs assembled on a model mRNA encoding a tetrapeptide followed by a UAA stop codon and report that initiation factors eIF3, eIF1, eIF1A, and eIF3j, a loosely associated subunit of eIF3, can promote recycling of eukaryotic... More