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Expression Levels Influence Ribosomal Frameshifting at the Tandem Rare Arginine Codons AGG_AGG and AGA_AGA in Escherichia coli

机译:表达水平影响在大肠杆菌中串联的稀有精氨酸密码子AGG_AGG和AGA_AGA的核糖体移码

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摘要

The rare codons AGG and AGA comprise 2% and 4%, respectively, of the arginine codons of Escherichia coli K-12, and their cognate tRNAs are sparse. At tandem occurrences of either rare codon, the paucity of cognate aminoacyl tRNAs for the second codon of the pair facilitates peptidyl-tRNA shifting to the +1 frame. However, AGG_AGG and AGA_AGA are not underrepresented and occur 4 and 42 times, respectively, in E. coli genes. Searches for corresponding occurrences in other bacteria provide no strong support for the functional utilization of frameshifting at these sequences. All sequences tested in their native context showed 1.5 to 11% frameshifting when expressed from multicopy plasmids. A cassette with one of these sequences singly integrated into the chromosome in stringent cells gave 0.9% frameshifting in contrast to two- to four-times-higher values obtained from multicopy plasmids in stringent cells and eight-times-higher values in relaxed cells. Thus, +1 frameshifting efficiency at AGG_AGG and AGA_AGA is influenced by the mRNA expression level. These tandem rare codons do not occur in highly expressed mRNAs.
机译:稀有密码子AGG和AGA分别占大肠杆菌K-12精氨酸密码子的2%和4%,它们的同源tRNA稀疏。在任一稀有密码子的串联出现时,该对第二个密码子的同源氨基酰基tRNA的稀缺性促进了肽基tRNA移向+1框。但是,在大肠杆菌基因中,AGG_AGG和AGA_AGA的代表性并不低,分别发生4和42次。在其他细菌中寻找相应事件的搜索没有为这些序列上移码的功能利用提供强有力的支持。从多拷贝质粒表达时,在其天然环境中测试的所有序列均显示1.5%至11%的移码。与在严格细胞中从多拷贝质粒获得的高两倍至四倍的值和在松弛细胞中获得高八倍的值相比,具有这些序列之一的盒在严格细胞中单独整合到染色体中的帧移位为0.9%。因此,在AGG_AGG和AGA_AGA处的+1移码效率受mRNA表达水平的影响。这些串联的稀有密码子不会出现在高表达的mRNA中。

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