Rushing B G, Yelton M M, Long S R
Stanford University, Department of Biological Sciences, CA 94305-5020.
Nucleic Acids Res. 1991 Feb 25;19(4):921-7. doi: 10.1093/nar/19.4.921.
The nodulation (nod) genes of the symbiont Rhizobium meliloti are transcriptionally controlled by protein activators in the nodD gene family. While NodD1 and NodD2 act in concert with small molecular weight inducers provided by the host legume plant, NodD3 is an inducer-independent activator of the nod promoters. We determined the sequence of the nodD3 gene, confirmed the expression of a 35 kDa protein in vitro, and determined the insertion points of five Tn5 insertions in the region of the nodD3 gene. We found the NodD3 amino acid sequence to be markedly diverged from the sequences of NodD1 and NodD2, which were more similar to the inducer-dependent NodD of another species, Rhizobium leguminosarum biovar viciae. The expression of nodD3 is not well understood, but involves at least SyrM, another positive activator related to the LysR-NodD family. One of the phenotypically mutant Tn5 insertions used in genetic studies of NodD3-dependent nod regulation lacks NodD3 protein as determined by Western blots, but another expresses about 50-60% of the wild type level. The location of these Tn5 insertions substantially upstream of the open reading frame for NodD3 suggests importance of relatively distant regulatory sequences for nodD3 expression. An insertion that did not cause a NodD3- phenotype is located in the extreme C-terminus of the protein coding region.
共生菌苜蓿中华根瘤菌的结瘤(nod)基因受nodD基因家族中的蛋白质激活剂转录调控。NodD1和NodD2与宿主豆科植物提供的小分子诱导物协同作用,而NodD3是nod启动子的独立于诱导物的激活剂。我们确定了nodD3基因的序列,在体外证实了一种35 kDa蛋白的表达,并确定了nodD3基因区域中五个Tn5插入的插入位点。我们发现NodD3的氨基酸序列与NodD1和NodD2的序列明显不同,NodD1和NodD2的序列与另一种豌豆根瘤菌生物变种的依赖诱导物的NodD更相似。nodD3的表达尚不清楚,但至少涉及SyrM,另一种与LysR-NodD家族相关的正激活剂。在依赖NodD3的结瘤调控的遗传研究中使用的一个表型突变的Tn5插入,经蛋白质免疫印迹法测定缺乏NodD3蛋白,但另一个表达量约为野生型水平的50 - 60%。这些Tn5插入位于NodD3开放阅读框上游相当远的位置,这表明相对较远的调控序列对nodD3表达很重要。一个未导致NodD3表型的插入位于蛋白质编码区的极端C末端。