Cren M, Kondorosi A, Kondorosi E
Institut des Sciences Végétales, CNRS, 91198 Gif-sur-Yvette, France.
Mol Microbiol. 1995 Feb;15(4):733-47. doi: 10.1111/j.1365-2958.1995.tb02381.x.
The synthesis of Rhizobium meliloti Nod signal molecules, encoded by the nod gene products, is finely regulated. A negative control of plasmid-borne nod gene expression is provided by the NolR repressor encoded by the chromosomal nolR gene. NolR was previously shown to downregulate the expression of the activator nodD1 gene and the common nodABC operon by binding to an overlapping region of the two promoters adjacent to the n1 nod-box (Kondorosi et al., 1989). We demonstrate here that NolR also controls the expression of two additional genes, nodD2 and nodM, but does not directly regulate the expression of the host-specific nod genes located downstream of the n2, n3 and n5 nod-boxes. Thus, the nod genes are differentially regulated by NolR and only those providing common nodulation functions, by determining the synthesis of the core Nod factor structure, are subjected to this negative regulation. Furthermore, NolR has a strong negative effect on the production of Nod metabolites, the level of which may serve as a fine-tuning mechanism for optimal nodulation, specific to host-plant genotypes. In addition, it elicits preferential synthesis of Nod factors carrying unsaturated C16 fatty acids. Expression of nolR was high both in the free-living bacterium and in the bacteroid and it was downregulated by its own product and by the nod gene inducer luteolin.
由结瘤基因产物编码的苜蓿根瘤菌结瘤信号分子的合成受到精细调控。染色体上的nolR基因编码的NolR阻遏蛋白对质粒携带的结瘤基因表达起到负调控作用。先前研究表明,NolR通过与n1结瘤框相邻的两个启动子的重叠区域结合,下调激活因子nodD1基因和共同结瘤基因nodABC操纵子的表达(孔多罗西等人,1989年)。我们在此证明,NolR还控制另外两个基因nodD2和nodM的表达,但不直接调控位于n2、n3和n5结瘤框下游的宿主特异性结瘤基因的表达。因此,结瘤基因受到NolR的差异调控,只有那些通过决定核心结瘤因子结构的合成来提供共同结瘤功能的基因才受到这种负调控。此外,NolR对结瘤代谢产物的产生有很强的负效应,其水平可能作为一种微调机制,针对宿主植物基因型实现最佳结瘤。此外,它还引发携带不饱和C16脂肪酸的结瘤因子的优先合成。nolR在自由生活的细菌和类菌体中表达都很高,并且受到其自身产物和结瘤基因诱导物木犀草素的下调。