Fisseha M, Gloudemans M, Gill R E, Kroos L
Department of Biochemistry, Michigan State University, East Lansing 48824, USA.
J Bacteriol. 1996 May;178(9):2539-50. doi: 10.1128/jb.178.9.2539-2550.1996.
omega 4403 is the site of a Tn5 lac insertion in the Myxococcus xanthus genome that fuses lacZ expression to a developmentally regulated promoter. Cell-cell interactions that occur during development, including C-signaling, are required for expression of Tn5 lac omega 4403. We have cloned DNA upstream of the omega 4403 insertion site, localized the promoter, and identified a potential open reading frame. From the deduced amino acid sequence, the gene disrupted by Tn5 lac omega 4403 appears to encode a serine protease that is dispensable for development. The gene begins to be expressed between 6 and 12 h after starvation initiates development, as determined by measuring mRNA or beta-galactosidase accumulation in cells containing Tn5 lac omega 4403. The putative transcriptional start site was mapped, and sequences centered near -10 and -35 bp relative to this site show some similarity to the corresponding regions of promoters transcribed by Escherichia coli sigma70 RNA polymerase. However, deletions showed that an essential promoter element lies between -80 and -72 bp, suggesting the possible involvement of an upstream activator protein. DNA downstream of -80 is sufficient for C-signal-dependent activation of this promoter. The promoter is not fully expressed when fusions are integrated at the Mx8 phage attachment site in the chromosome. Titration of a limiting factor by two copies of the regulatory region (one at the attachment site and one at the native site) can, in part, explain the reduced expression. We speculate that the remaining difference may be due to an effect of chromosomal position. These results provide a basis for studies aimed at identifying regulators of C-signal-dependent gene expression.
ω4403是黄色黏球菌基因组中Tn5 lac插入位点,该位点将lacZ表达与一个发育调控启动子融合。发育过程中发生的细胞间相互作用,包括C信号传导,是Tn5 lac ω4403表达所必需的。我们克隆了ω4403插入位点上游的DNA,定位了启动子,并鉴定出一个潜在的开放阅读框。从推导的氨基酸序列来看,被Tn5 lac ω4403破坏的基因似乎编码一种丝氨酸蛋白酶,该蛋白酶对发育并非必需。通过测量含有Tn5 lac ω4403的细胞中mRNA或β-半乳糖苷酶的积累来确定,该基因在饥饿引发发育后的6至12小时开始表达。绘制了推定的转录起始位点,相对于该位点,位于-10和-35 bp附近的序列与大肠杆菌σ70 RNA聚合酶转录的启动子的相应区域有一些相似性。然而,缺失表明一个必需的启动子元件位于-80至-72 bp之间,这表明可能涉及上游激活蛋白。-80下游的DNA足以实现该启动子的C信号依赖性激活。当融合体整合到染色体上的Mx8噬菌体附着位点时,启动子不能完全表达。两个拷贝的调控区域(一个在附着位点,一个在天然位点)对限制因子的滴定可以部分解释表达降低的原因。我们推测剩余的差异可能是由于染色体位置的影响。这些结果为旨在鉴定C信号依赖性基因表达调节因子的研究提供了基础。