John Innes Institute, Colney Lane, Norwich NR4 7UH, UK.
EMBO J. 1985 Dec 16;4(13A):3369-73. doi: 10.1002/j.1460-2075.1985.tb04092.x.
To analyse nod gene expression in Rhizobium leguminosarum, a broad host-range lacZ protein fusion vector was constructed. Two protein fusions, nodC-lacZ and nodD-lacZ, were used to measure the regulation of expression of the promoters of the nodA,B,C and the nodD transcripts by measuring the induced levels of beta-galactosidase activity in R. leguminosarum. In the absence of plant root exudate the nodD-lacZ hybrid was expressed but the nodC-lacZ hybrid was not. The expression of the nodD-lacZ hybrid was repressed in R. leguminosarum strains containing an intact cloned nodD gene indicating that the nodD gene is autoregulatory. The induction of the nodC-lacZ hybrid required both the nodD gene and a component present in plant root exudate. Therefore the nodD gene acts both as a repressor and as an activator of gene expression. The nodD gene is adjacent to nodA and transcribed divergently from nodA,B,C with only approximately 300 nucleotides between the coding regions of nodA and nodD. Within this intergenic region is a unique BclI site and, using nodC-lacZ or nodD-lacZ translational fusions with this BclI site as an end point, no induction of nodC-lacZ or nodD-lacZ was observed. Therefore the promoters of nodD and nodA,B,C overlap at least at this region, and the regulation of these overlapping promoters appears to be controlled by the nodD protein which becomes an activator only in the presence of a component from plant exudate.
为了分析根瘤菌(Rhizobium leguminosarum)nod 基因的表达,构建了一个广谱宿主范围的 lacZ 蛋白融合载体。利用两个蛋白融合物 nodC-lacZ 和 nodD-lacZ,通过测量β-半乳糖苷酶活性的诱导水平,来测量 nodA、B、C 启动子和 nodD 转录物的表达调控。在没有植物根分泌物的情况下,nodD-lacZ 杂种被表达,但 nodC-lacZ 杂种没有被表达。在含有完整克隆 nodD 基因的根瘤菌菌株中,nodD-lacZ 杂种的表达受到抑制,表明 nodD 基因是自我调控的。nodC-lacZ 杂种的诱导需要 nodD 基因和植物根分泌物中的一个成分。因此,nodD 基因既作为抑制剂又作为激活剂来调节基因表达。nodD 基因与 nodA 相邻,并从 nodA、B、C 转录方向相反,在 nodA 和 nodD 的编码区之间只有大约 300 个核苷酸。在这个基因间区有一个独特的 BclI 位点,利用 nodC-lacZ 或 nodD-lacZ 与这个 BclI 位点的翻译融合作为终点,没有观察到 nodC-lacZ 或 nodD-lacZ 的诱导。因此,nodD 和 nodA、B、C 的启动子至少在这个区域重叠,并且这些重叠启动子的调节似乎受到 nodD 蛋白的控制,该蛋白只有在植物分泌物中的一个成分存在时才成为激活剂。