Oger P, Kim K S, Sackett R L, Piper K R, Farrand S K
Department of Crop Sciences, University of Illinois at Urbana-Champaign, Urbana 61801, USA.
Mol Microbiol. 1998 Jan;27(2):277-88. doi: 10.1046/j.1365-2958.1998.00671.x.
Conjugal transfer of Agrobacterium tumefaciens Ti plasmids is regulated by two hierarchical signalling systems. Transfer is dependent on a subset of opines produced by the plant tumours induced by the bacterium. Induction also requires an acyl-homoserine lactone signal, called AAI, that is produced by the bacteria themselves. AAI is the co-inducer for TraR, the transcriptional activator required for expression of the tra regulon. Octopine induces conjugation of the octopine-mannityl opine-type Ti plasmids by regulating the expression of traR via OccR, the octopine-dependent activator of the opine regulon. We have discovered a second traR-like gene, trlR, on the octopine-mannityl opine-type Ti plasmids pTi15955 and pTiR10. This gene is located in an operon coding for a mannopine transport system and is expressed as part of the mannityl opine regulon. Sequence analysis indicated that trlR is a frameshift allele of traR, and the resulting protein lacks the carboxy-terminal domain thought to constitute the DNA-binding region of TraR. Expression of trlR inhibited octopine-induced conjugation of pTi15955 and pTiR10 by suppressing the TraR-mediated transcription of the tra and trb operons. Although TrlR had no effect on the expression of traR, TraR activated the expression of trlR. Southern hybridizations indicated that several other Ti and opine-catabolic plasmids contain more than one copy of genes homologous to traR. We propose that trlR is a dominant negative allele of traR and that TrlR inhibits conjugation by forming inactive heteromultimers with TraR.
根癌土壤杆菌Ti质粒的接合转移受两个层次信号系统调控。转移依赖于该细菌诱导产生的植物肿瘤所产生的一部分冠瘿碱。诱导作用还需要一种由细菌自身产生的酰基高丝氨酸内酯信号,称为AAI。AAI是TraR的共诱导物,TraR是tra操纵子表达所需的转录激活因子。章鱼碱通过章鱼碱依赖的冠瘿碱操纵子激活因子OccR调节traR的表达,从而诱导章鱼碱-甘露碱型Ti质粒的接合。我们在章鱼碱-甘露碱型Ti质粒pTi15955和pTiR10上发现了第二个类traR基因trlR。该基因位于一个编码甘露碱转运系统的操纵子中,并作为甘露碱型冠瘿碱操纵子的一部分表达。序列分析表明trlR是traR的移码等位基因,所产生的蛋白质缺乏被认为构成TraR DNA结合区域的羧基末端结构域。trlR的表达通过抑制TraR介导的tra和trb操纵子的转录,抑制了章鱼碱诱导的pTi15955和pTiR10的接合。虽然TrlR对traR的表达没有影响,但TraR激活了trlR的表达。Southern杂交表明,其他几种Ti质粒和冠瘿碱分解代谢质粒含有多个与traR同源的基因拷贝。我们提出trlR是traR的显性负等位基因,TrlR通过与TraR形成无活性的异源多聚体来抑制接合。