Anisimov Roman, Brem Daniela, Heesemann Jürgen, Rakin Alexander
Max von Pettenkofer-Institute of Hygiene and Medical Microbiology Pettenkofer Strasse 9a, 80336 Munich, Germany.
FEMS Microbiol Lett. 2005 Sep 1;250(1):27-32. doi: 10.1016/j.femsle.2005.06.040.
Genes of Yersiniae spp. involved in production of the siderophore yersiniabactin are located on the high-pathogenicity island (HPI). Their transcription is controlled by the AraC/XilS-like transcriptional regulator YbtA encoded within the HPI. YbtA-regulated divergent and overlapping ybtA and irp6 promoters contain three YbtA binding sites, RS1, RS2 and RS3. Deleting RSs systematically and using ybtA and irp6 transcriptional fusions, we determined that different modes of YbtA binding are responsible for activation of irp6 and repression of ybtA. Based on these data, we propose a model of irp6 and ybtA promoter regulation.
参与耶尔森菌素(yersiniabactin)合成的耶尔森氏菌属(Yersiniae spp.)基因位于高致病性岛(HPI)上。它们的转录由HPI内编码的AraC/XilS样转录调节因子YbtA控制。YbtA调节的 divergent和重叠的ybtA及irp6启动子包含三个YbtA结合位点,即RS1、RS2和RS3。通过系统删除RS并使用ybtA和irp6转录融合体,我们确定YbtA不同的结合模式分别负责irp6的激活和ybtA的抑制。基于这些数据,我们提出了irp6和ybtA启动子调控模型。