Danot O, Raibaud O
Unité de Génétique Moléculaire, Unité de Recherche Associée 1149 du Centre National de la Recherche Scientifique, Institut Pasteur, Paris, France.
Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):10999-1003. doi: 10.1073/pnas.90.23.10999.
The MalT-dependent promoters of the enterobacteria belong to a small family of positively regulated prokaryotic promoters in which the activator protein recognizes short asymmetric nucleotide sequences present in several locations and orientations. We demonstrate that active MalT-dependent semisynthetic promoters can be constructed by using a synthetic decanucleotide as the MalT site and random nucleotide sequences as connecting sequences, provided that the location and orientation of the sites are the same as in natural MalT-dependent promoters. Strikingly, the induced level of promoter activity and the induction factor of each semisynthetic promoter are identical to those of its natural counterpart, in spite of considerable differences in their nucleotide sequences. The study of these semisynthetic promoters confirms the importance of the structural motif formed by two MalT sites in a direct repeat. This motif is involved in promoter activation either alone or in conjunction with a third MalT site, proximal with respect to the transcription start site. In this latter configuration, the promoters are active irrespective of the orientation of the repeat, and they retain at least some activity when the distance between the repeat and the proximal site is increased, provided that the alignment along the axis of the helix is conserved.
肠道杆菌中依赖MalT的启动子属于一小类正调控的原核启动子家族,其中激活蛋白识别存在于多个位置和方向的短不对称核苷酸序列。我们证明,通过使用合成的十聚体核苷酸作为MalT位点,并使用随机核苷酸序列作为连接序列,可以构建有活性的依赖MalT的半合成启动子,前提是这些位点的位置和方向与天然依赖MalT的启动子相同。令人惊讶的是,尽管每个半合成启动子的核苷酸序列存在相当大的差异,但其启动子活性的诱导水平和诱导因子与其天然对应物相同。对这些半合成启动子的研究证实了由两个MalT位点以直接重复形式形成的结构基序的重要性。该基序单独或与相对于转录起始位点近端的第三个MalT位点一起参与启动子激活。在后一种构型中,启动子无论重复序列的方向如何都是有活性的,并且当重复序列与近端位点之间的距离增加时,只要沿螺旋轴的排列保持保守,它们至少保留一些活性。