Fisher R F, Long S R
Stanford University, Department of Biological Sciences, CA 94305-5020.
J Mol Biol. 1993 Oct 5;233(3):336-48. doi: 10.1006/jmbi.1993.1515.
The Rhizobium meliloti nodD gene products are positive transcriptional activators of genes required for early stages of nodule morphogenesis in the R. meliloti-alfalfa symbiosis (nod genes). The regulatory activity of NodD, a member of the LysR family of activator proteins, is mediated in part through its binding to conserved DNA sequences termed nod boxes which lie upstream of the inducible nod genes. Here we use interference footprinting to identify two NodD binding sites in the nodA, nodF and nodH nod boxes. These two binding sites are located on the same face of the DNA helix and can be separated by an additional 10 bp with retention of activity. By systematic alteration of the phasing of the two binding sites on the DNA helix, we showed that only constructs which contain both sites on the same side of the helix are recognized by NodD as determined by migration retardation assay and by in vivo activation of nod box-lacZ fusions. Moreover, NodD apparently induces a bend in the DNA upon binding at the nod box as shown by migration retardation behavior of circularly permuted nod box fragments.
苜蓿中华根瘤菌的nodD基因产物是苜蓿中华根瘤菌 - 苜蓿共生中根瘤形态发生早期所需基因(nod基因)的正转录激活因子。NodD是激活蛋白LysR家族的成员,其调节活性部分通过与位于可诱导nod基因上游的保守DNA序列(称为nod框)结合来介导。在这里,我们使用干涉足迹法来鉴定nodA、nodF和nodH nod框中的两个NodD结合位点。这两个结合位点位于DNA螺旋的同一面上,并且可以通过额外的10个碱基对分开而保持活性。通过系统改变DNA螺旋上两个结合位点的相位,我们表明,只有在螺旋同一侧包含两个位点的构建体才能被NodD识别,这是通过迁移率阻滞试验和nod框 - lacZ融合体的体内激活来确定的。此外,如环状排列的nod框片段的迁移率阻滞行为所示,NodD在结合nod框时显然会诱导DNA弯曲。