Vögele K, Schwartz E, Welz C, Schiltz E, Rak B
Institut für Biologie III, Universität Freiburg, FRG.
Nucleic Acids Res. 1991 Aug 25;19(16):4377-85. doi: 10.1093/nar/19.16.4377.
IS150 contains two tandem, out-of-phase, overlapping genes, ins150A and ins150B, which are controlled by the same promoter. These genes encode proteins of 19 and 31 kD, respectively. A third protein of 49 kD is a transframe gene product consisting of domains encoded by both genes. Specific -1 ribosomal frameshifting is responsible for the synthesis of the large protein. Expression of ins150B also involves frameshifting. The IS150 frameshifting signals operate with a remarkably high efficiency, causing about one third of the ribosomes to switch frame. All of the signals required for this process are encoded in a 83-bp segment of the element. The heptanucleotide A AAA AAG and a potential stem-loop-forming sequence mark the frameshifting site. Similar sequence elements are found in -1 frameshifting regions of bacterial and retroviral genes. A mutation within the stem-loop sequence reduces the rate of frameshifting by about 80%. Artificial transposons carrying this mutation transpose at a normal frequency, but form cointegrates at a approximately 100-fold reduced rate.
IS150含有两个串联、异相、重叠的基因,即ins150A和ins150B,它们由同一个启动子控制。这些基因分别编码19kD和31kD的蛋白质。第三种49kD的蛋白质是一种由两个基因编码的结构域组成的移码基因产物。特定的 -1核糖体移码负责大蛋白的合成。ins150B的表达也涉及移码。IS150移码信号的运作效率非常高,导致约三分之一的核糖体改变读码框。这一过程所需的所有信号都编码在该元件的一个83bp片段中。七核苷酸AAAAAAG和一个潜在的茎环形成序列标记了移码位点。在细菌和逆转录病毒基因的 -1移码区域也发现了类似的序列元件。茎环序列内的一个突变使移码率降低了约80%。携带这种突变的人工转座子以正常频率转座,但形成共整合体的速率大约降低了100倍。