Pahel G, Rothstein D M, Magasanik B
J Bacteriol. 1982 Apr;150(1):202-13. doi: 10.1128/jb.150.1.202-213.1982.
The glnG gene product is both a positive regulator and a negative regulator of the expression of glnA, the structural gene for glutamine synthetase, as well as a positive regulator of the expression of a number of genes whose products are involved in the uptake and degradation of nitrogen-containing compounds. The regulation of beta-galactosidase in various strains containing a Mu d1 (lac bla) insertion within glnG leads to the following conclusions regarding the expression of this gene: (i) like the synthesis of glutamine synthetase, the synthesis of the glnG product is regulated in response to the nitrogen source; (ii) high-level expression of glnG under nitrogen-limiting growth conditions depends on transcription initiated at the glnA promoter; and (iii) there is a second, glnA-distal promoter for glnG, whose activity is negatively controlled by the glnG product. Thus, the glnG product regulates the synthesis of the glnG product at two distinct promoters (positively and negatively at the glnA promoter and negatively at the glnA-distal promoter). In addition, a high level of glnG product, corresponding to the level produced by initiation of transcription at the glnA promoter under nitrogen-limiting conditions, is necessary for activation of histidase synthesis. The lower level of glnG product originating from transcription initiated at the glnA-distal promoter is not sufficient to activate histidase synthesis, but is sufficient to activate fully and to repress glnA expression.
谷氨酰胺合成酶结构基因glnA的表达,其谷氨酰胺合成酶的产物既是正调控因子又是负调控因子,同时也是许多基因表达的正调控因子,这些基因的产物参与含氮化合物的摄取和降解。在含有glnG内Mu d1(lac bla)插入片段的各种菌株中对β-半乳糖苷酶的调控,得出了关于该基因表达的以下结论:(i)与谷氨酰胺合成酶的合成一样,glnG产物的合成受氮源调控;(ii)在氮限制生长条件下,glnG的高水平表达取决于从glnA启动子起始的转录;(iii)存在第二个位于glnA远端的glnG启动子,其活性受glnG产物的负调控。因此,glnG产物在两个不同的启动子处调控glnG产物的合成(在glnA启动子处正调控和负调控,在glnA远端启动子处负调控)。此外,高水平的glnG产物,对应于在氮限制条件下从glnA启动子起始转录所产生的水平,是激活组氨酸酶合成所必需的。源自glnA远端启动子起始转录的较低水平的glnG产物不足以激活组氨酸酶合成,但足以完全激活并抑制glnA表达。