Brocklehurst K R, Megit S J, Morby A P
Syngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire RG42 6EY, UK.
Biochem Biophys Res Commun. 2003 Aug 22;308(2):234-9. doi: 10.1016/s0006-291x(03)01366-4.
cadR from Pseudomonas aeruginosa encodes a transcriptional regulatory protein which responds to Cd(II)>>Zn(II)>Hg(II) at its cognate promoter PcadA. CadR will also act to induce transcription at the Escherichia coli ZntR cognate promoter, PzntA, however, the induction profile is altered to Hg(II)>Cd(II)>Zn(II). Two separate single base pair deletions within PzntA result in further alteration of relative specificity in metal-ion induction profile for CadR. This demonstrates that the operator/promoter sequence can play a role in defining optimal ligand response and that for these regulators specificity is not solely a function of the regulatory protein.
来自铜绿假单胞菌的CadR编码一种转录调节蛋白,该蛋白在其同源启动子PcadA处对Cd(II)>>Zn(II)>Hg(II)作出反应。然而,CadR也会在大肠杆菌ZntR同源启动子PzntA处诱导转录,不过诱导模式变为Hg(II)>Cd(II)>Zn(II)。PzntA内两个单独的单碱基对缺失导致CadR在金属离子诱导模式下的相对特异性进一步改变。这表明操纵子/启动子序列在定义最佳配体反应中可以发挥作用,并且对于这些调节因子来说,特异性不仅仅是调节蛋白的功能。