Roh Jong-Bok, Lee Mi-Ae, Lee Hyun-Jung, Kim Sung-Min, Cho Yona, Kim You-Jin, Seok Yeong-Jae, Park Soon-Jung, Lee Kyu-Ho
Department of Environmental Science, Hankuk University of Foreign Studies, Yongin, Kyunggi-Do 449-791, Seoul, South Korea.
J Biol Chem. 2006 Nov 17;281(46):34775-84. doi: 10.1074/jbc.M607844200. Epub 2006 Sep 12.
Vibrio vulnificus causes diseases through actions of various virulence factors, including the elastase encoded by the vvpE gene. Through transposon mutagenesis of V. vulnificus, vvpE expression was shown to be increased by luxO mutation. Since the vvpE gene is known to be positively regulated by SmcR via direct binding to the vvpE promoter, the role of LuxO in smcR expression was investigated. The luxAB-transcriptional fusions containing different lengths of the smcR promoter region indicated that the smcR transcription was negatively regulated by LuxO and that a specific upstream region of the smcR gene was required for this repression. Since LuxO is a known member of positive regulators, the negative regulation of smcR transcription by LuxO prompted us to identify the factor(s) linking LuxO and smcR transcription. LuxT was isolated in a ligand fishing experiment using the smcR upstream region as bait, and smcR expression was increased by luxT mutation. Recombinant LuxT bound to a specific upstream region of the smcR gene, -154 to -129 relative to the smcR transcription start site. The expression of luxT was positively regulated by LuxO, and the luxT promoter region contained a putative LuxO-binding site. Mutagenesis of the LuxO-binding site in the luxT promoter region resulted in a loss of transcriptional control by LuxO. Therefore, this study demonstrates a transcriptional regulatory cascade for elastase production, where LuxO activates luxT transcription and LuxT represses smcR transcription.
创伤弧菌通过多种毒力因子的作用引发疾病,其中包括由vvpE基因编码的弹性蛋白酶。通过对创伤弧菌进行转座子诱变,发现luxO突变可使vvpE表达增加。由于已知vvpE基因受SmcR通过直接结合其启动子正向调控,因此对LuxO在smcR表达中的作用进行了研究。含有不同长度smcR启动子区域的luxAB转录融合表明,LuxO对smcR转录起负调控作用,且smcR基因的一个特定上游区域是这种抑制作用所必需的。由于LuxO是已知的正调控因子成员,LuxO对smcR转录的负调控促使我们去鉴定连接LuxO和smcR转录的因子。在一项以smcR上游区域为诱饵的配体垂钓实验中分离出了LuxT,且luxT突变会使smcR表达增加。重组的LuxT结合到smcR基因的一个特定上游区域,相对于smcR转录起始位点为-154至-129。luxT的表达受LuxO正向调控,且luxT启动子区域包含一个假定的LuxO结合位点。对luxT启动子区域中LuxO结合位点进行诱变导致失去了LuxO的转录调控。因此,本研究证明了弹性蛋白酶产生的转录调控级联,其中LuxO激活luxT转录,而LuxT抑制smcR转录。