Ruiz-Echevarría M J, Berzal-Herranz A, Gerdes K, Díaz-Orejas R
Centro de Investigaciones Biológicas (CSIC), Madrid, Spain.
Mol Microbiol. 1991 Nov;5(11):2685-93. doi: 10.1111/j.1365-2958.1991.tb01977.x.
Stability mediated by the parD system of plasmid R1 is modulated by a killer protein, Kid, and by an antagonist of this function, Kis. Determination of the 5' ends of ParD transcripts, revealed that the genes coding for these proteins are transcribed from a single promoter. Analysis of the 3' end of the ParD RNAs indicated the existence of two transcripts: one of them coding for the Kis and Kid proteins, and the other coding only for Kis. Analysis of the effects of parD+ and kis+ recombinants on the beta-galactosidase levels expressed by different transcriptional and translational parD-lacZ fusions, and on the ParD RNA levels determined by a derepressed parD mutant, indicated that the Kis and Kid proteins repress coordinately the parD system at the transcriptional level. We discuss the relevance of these results in terms of the activities of the Kis and Kid proteins and in the context of the stabilization mediated by parD.
质粒R1的parD系统介导的稳定性受一种杀伤蛋白Kid以及该功能的拮抗剂Kis的调节。对ParD转录本5'端的测定表明,编码这些蛋白质的基因是从一个单一启动子转录而来的。对ParD RNA 3'端的分析表明存在两种转录本:其中一种编码Kis和Kid蛋白,另一种仅编码Kis。分析parD+和kis+重组体对不同转录和翻译的parD-lacZ融合体所表达的β-半乳糖苷酶水平,以及对由去阻遏的parD突变体所测定的ParD RNA水平的影响,表明Kis和Kid蛋白在转录水平上协同抑制parD系统。我们根据Kis和Kid蛋白的活性以及在parD介导的稳定性背景下讨论了这些结果的相关性。