Morschhäuser J, Uhlin B E, Hacker J
Lehrstuhl für Mikrobiologie im Theodor-Boveri-Institut, Würzburg, FRG.
Mol Gen Genet. 1993 Apr;238(1-2):97-105. doi: 10.1007/BF00279536.
The sfa determinant codes for S fimbrial adhesins which constitute adherence factors of pathogenic Escherichia coli strains. We have recently shown that the sfa determinant is transcribed from three promoters, pA, pB, and pC. In comparison with the promoters pB and pC, promoter pA, which is located in front of the structural gene sfaA, showed very weak activity. Here we have determined the exact positions of the mRNA start points by primer extension studies. We have also shown that mRNAs of 500, 700 and 1400 bases can be detected using oligonucleotide probes specific for the genes sfaB, sfaC and sfaA. SfaB and SfaC are positive regulators influencing fimbriation and the production of the S-specific adhesin which is encoded by the gene sfaS located in the distal half of the determinant. In addition, it is demonstrated that SfaB and SfaC interfere with the regulatory effect of the histone-like protein H-NS, encoded by a locus termed drdX or osmZ. In a drdX+ strain the regulators are necessary for transcription of the sfa determinant. In contrast, sfa expression is activator-independent in a drdX- strain. In this latter genetic background, a substantial fraction of the sfa transcripts is initiated from promoter pA. On the basis of these data we discuss a model for the regulation of this adhesin-specific determinant.
sfa决定簇编码S菌毛粘附素,其构成致病性大肠杆菌菌株的粘附因子。我们最近发现sfa决定簇由三个启动子pA、pB和pC转录。与启动子pB和pC相比,位于结构基因sfaA之前的启动子pA活性非常弱。在此,我们通过引物延伸研究确定了mRNA起始点的确切位置。我们还表明,使用针对基因sfaB、sfaC和sfaA的寡核苷酸探针可以检测到500、700和1400个碱基的mRNA。SfaB和SfaC是正向调节因子,影响菌毛形成以及由位于决定簇远端一半的基因sfaS编码的S特异性粘附素的产生。此外,还证明SfaB和SfaC会干扰由称为drdX或osmZ的基因座编码的组蛋白样蛋白H-NS的调节作用。在drdX+菌株中,这些调节因子对于sfa决定簇的转录是必需的。相反,在drdX-菌株中,sfa表达不依赖于激活剂。在这种后一种遗传背景下,相当一部分sfa转录本从启动子pA起始。基于这些数据,我们讨论了这种粘附素特异性决定簇的调节模型。