Chevrier-Miller M, Jacques N, Raibaud O, Dreyfus M
Laboratoire de Génétique Moléculaire (CNRS D 1302), ENS, Paris, France.
Nucleic Acids Res. 1990 Oct 11;18(19):5787-92. doi: 10.1093/nar/18.19.5787.
In Escherichia coli transcription of individual genes generally requires concomitant translation, and thus the decay of mRNAs cannot be studied without the complication of translation. Here we have used T7 RNA polymerase to transcribe in vivo lacZ genes carrying ribosome binding sites of variable efficiency. We show that neither cell viability nor growth rate is affected by the T7-driven transcription of these genes, provided that they are present as single chromosomal copy. Furthermore, transcription is now completely uncoupled from translation, allowing large amounts of even completely untranslated mRNAs to be synthesized. Taking advantage of these features, we discuss the influence of the frequency of translation upon the processing and degradation of the lac message.
在大肠杆菌中,单个基因的转录通常需要伴随翻译进行,因此,如果不考虑翻译带来的复杂性,就无法研究mRNA的衰减。在这里,我们使用T7 RNA聚合酶在体内转录携带不同效率核糖体结合位点的lacZ基因。我们发现,只要这些基因以单染色体拷贝形式存在,T7驱动的转录对细胞活力和生长速率均无影响。此外,转录现在与翻译完全解偶联,从而能够合成大量甚至完全未翻译的mRNA。利用这些特性,我们讨论了翻译频率对lac信息的加工和降解的影响。