Tsuchihashi Z
Howard Hughes Medical Institute, Stanford University School of Medicine, CA 94305.
Nucleic Acids Res. 1991 May 11;19(9):2457-62. doi: 10.1093/nar/19.9.2457.
Production of the gamma subunit of Escherichia coli DNA polymerase III holoenzyme is dependent on a very efficient translational frameshif in the dnaX gene. I used an E. coli in vitro translation system to analyze the mechanism of this frameshifting event. In this system, gamma was produced almost to the same extent as the inframe translation product, tau, suggesting that efficient frameshifting was reproduced in vitro. Coupling with transcription was not necessary for frameshifting. Addition of purified tau or gamma had no effect on the frameshifting process suggesting the absence of direct feedback regulation. By use of mutant genes, a strong pausing site was identified at or very close to the frameshift site. This pausing was apparently caused by a potential stem-loop structure which was previously shown to enhance frameshifting. Thus, enhancement of frameshifting by this putative stem-loop seems to be mediated by the translation pausing at the frameshift site. Despite the apparent structural similarity of the dnaX frameshift site to that of the eukaryotic retroviral genes, dnaX mRNA synthesized in vitro failed to direct the production of gamma in eukaryotic translation systems. This suggests that frameshifting in the dnaX gene depends on components specific to the E. coli translation system.
大肠杆菌DNA聚合酶III全酶γ亚基的产生依赖于dnaX基因中一种非常有效的翻译移码。我使用大肠杆菌体外翻译系统来分析这种移码事件的机制。在这个系统中,γ的产生程度几乎与框内翻译产物tau相同,这表明在体外再现了高效的移码。移码不需要与转录偶联。添加纯化的tau或γ对移码过程没有影响,这表明不存在直接的反馈调节。通过使用突变基因,在移码位点或非常接近移码位点处鉴定出一个强暂停位点。这种暂停显然是由一个潜在的茎环结构引起的,该结构先前已被证明可增强移码。因此,这种假定的茎环对移码的增强作用似乎是由移码位点处的翻译暂停介导的。尽管dnaX移码位点与真核逆转录病毒基因的移码位点在结构上有明显相似性,但体外合成的dnaX mRNA在真核翻译系统中未能指导γ的产生。这表明dnaX基因中的移码依赖于大肠杆菌翻译系统特有的成分。