McFall E, Nikam S S, Palchaudhuri S
Department of Microbiology, New York University School of Medicine, New York 10016.
J Bacteriol. 1991 Feb;173(3):1161-7. doi: 10.1128/jb.173.3.1161-1167.1991.
Single-base-pair changes well upstream of its transcription initiation site resulted in partially to fully constitutive expression of the D-serine deaminase structural gene, dsdA, independently of the cyclic AMP-cyclic AMP-binding protein complex and of the specific D-serine deaminase activator protein. These promoter mutations appear to define a consensus sequence that is repeated several times. Basal expression of dsdA+ was also strongly enhanced by subcloning on multicopy plasmids, by the DNA gyrase inhibitor novobiocin, and in dsdC(Con) mutants by increasing growth temperature. These results suggest that activation of dsdA+ expression by the dsdC-encoded protein involves distortion of promoter DNA. A dsdA translation start at bp -731 was verified by subcloning of dsdC+. Plasmid-specified activator at a high concentration interfered with chromosomal dsdC(Con) expression, and the interference was enhanced by deletion of most of the intergenic region from the plasmid. Even at a high concentration, however, plasmid-specified activator did not activate expression of chromosomal dsdA+, and in one case it was actually repressive. These results confirm the strong cis tropism of plasmid-specified dsdC-encoded protein and suggest that it is mediated by multiple sites in the dsdA-dsdC intergenic region.
在其转录起始位点上游很远的单碱基对变化导致D - 丝氨酸脱氨酶结构基因dsdA部分或完全组成型表达,这与环腺苷酸 - 环腺苷酸结合蛋白复合物以及特定的D - 丝氨酸脱氨酶激活蛋白无关。这些启动子突变似乎定义了一个重复多次的共有序列。通过在多拷贝质粒上亚克隆、DNA旋转酶抑制剂新生霉素以及在dsdC(Con)突变体中提高生长温度,dsdA + 的基础表达也得到了强烈增强。这些结果表明,由dsdC编码的蛋白质对dsdA + 表达的激活涉及启动子DNA的扭曲。通过dsdC + 的亚克隆验证了dsdA在bp - 731处的翻译起始。高浓度的质粒指定激活剂干扰了染色体dsdC(Con)的表达,并且通过从质粒中缺失大部分基因间区域,这种干扰得到增强。然而,即使在高浓度下,质粒指定激活剂也不激活染色体dsdA + 的表达,并且在一种情况下它实际上是抑制性的。这些结果证实了质粒指定的dsdC编码蛋白的强顺式趋向性,并表明它是由dsdA - dsdC基因间区域中的多个位点介导的。