Department of Life Science, Sogang University, Seoul, Korea.
Key Laboratory of Ministry of Education for Gastrointestinal Cancer Research Center for Molecular Medicine, Fujian Medical University, Fuzhou, Fujian, People's Republic of China.
Sci Rep. 2019 Dec 27;9(1):20135. doi: 10.1038/s41598-019-56855-4.
LeuO plays the role of a master regulator in the cyclic-L-phenylalanine-L-proline (cFP)-dependent signaling pathway in Vibrio vulnificus. cFP, as shown through isothermal titration calorimetry analysis, binds specifically to the periplasmic domain of ToxR. Binding of cFP triggers a change in the cytoplasmic domain of ToxR, which then activates transcription of leuO encoding a LysR-type regulator. LeuO binds to the region upstream of its own coding sequence, inhibiting its own transcription and maintaining a controlled level of expression. A five-bp deletion in this region abolished expression of LeuO, but a ten-bp deletion did not, suggesting that a DNA bending mechanism is involved in the regulation. Furthermore, binding of RNA polymerase was significantly lower both in the deletion of the ToxR binding site and in the five-bp deletion, but not in the ten-bp deletion, as shown in pull-down assays using an antibody against RNA polymerase subunit α. In summary, multiple factors are involved in control of the expression of LeuO, a master regulator that orchestrates downstream regulators to modulate factors required for survival and pathogenicity of the pathogen.
LeuO 在创伤弧菌中循环-L-苯丙氨酸-L-脯氨酸(cFP)依赖信号通路中充当主调控因子。正如等温滴定量热分析所表明的那样,cFP 特异性结合 ToxR 的周质域。cFP 的结合引发 ToxR 胞质域的变化,然后激活编码 LysR 型调控因子的 leuO 的转录。LeuO 结合其自身编码序列的上游区域,抑制自身转录并维持受控的表达水平。该区域的五碱基缺失消除了 LeuO 的表达,但十碱基缺失则没有,这表明 DNA 弯曲机制参与了调控。此外,正如使用针对 RNA 聚合酶亚基 α 的抗体进行下拉测定所表明的那样,在 ToxR 结合位点缺失和五碱基缺失的情况下,RNA 聚合酶的结合显著降低,但在十碱基缺失的情况下则没有。总之,多个因素参与控制 LeuO 的表达,LeuO 是一个主调控因子,它协调下游调控因子来调节病原体生存和致病性所需的因素。