Sekine Y, Ohtsubo E
Institute of Applied Microbiology, University of Tokyo, Japan.
Mol Gen Genet. 1992 Nov;235(2-3):325-32. doi: 10.1007/BF00279377.
The transposase encoded by insertion sequence IS1 is produced from two out-of-phase reading frames (insA and B'-insB) by translational frameshifting, which occurs within a run of six adenines in the -1 direction. To determine the sequence essential for frameshifting, substitution mutations were introduced within the region containing the run of adenines and were examined for their effects on frameshifting. Substitutions at each of three (2nd, 3rd and 4th) adenine residues in the run, which are recognized by tRNA(Lys) reading insA, caused serious defects in frameshifting, showing that the three adenine residues are essential for frameshifting. The effects of substitution mutations introduced in the region flanking the run of adenines and in the secondary structures located downstream were, however, small, indicating that such a region and structures are not essential for frameshifting. Deletion of a region containing the termination codon of insA caused a decrease in beta-galactosidase activity specified by the lacZ fusion plasmid in frame with B'-insB. Exchange of the wild-type termination codon of insA for a different one or introduction of an additional termination codon in the region upstream of the native termination codon caused an increase in beta-galactosidase activity, indicating that the termination codon in insA affects the efficiency of frameshifting.
插入序列IS1编码的转座酶由两个不同相位的阅读框(insA和B'-insB)通过翻译移码产生,该移码发生在六个腺嘌呤组成的序列中,移码方向为-1。为了确定移码所必需的序列,在包含腺嘌呤序列的区域内引入了替换突变,并检测其对移码的影响。在该序列中被读取insA的tRNA(Lys)识别的三个(第2、3和4个)腺嘌呤残基处的替换,导致移码出现严重缺陷,表明这三个腺嘌呤残基对移码至关重要。然而,在腺嘌呤序列侧翼区域和下游二级结构中引入的替换突变的影响较小,表明此类区域和结构对移码并非必需。删除包含insA终止密码子的区域会导致与B'-insB读框一致的lacZ融合质粒所指定的β-半乳糖苷酶活性降低。将insA的野生型终止密码子替换为另一个密码子或在天然终止密码子上游区域引入额外的终止密码子会导致β-半乳糖苷酶活性增加,表明insA中的终止密码子会影响移码效率。