Szurmant Hendrik, Nelson Kristine, Kim Eun-Ja, Perego Marta, Hoch James A
Division of Cellular Biology, Mail code MEM-116, Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
J Bacteriol. 2005 Aug;187(15):5419-26. doi: 10.1128/JB.187.15.5419-5426.2005.
Of the numerous two-component signal transduction systems found in bacteria, only a very few have proven to be essential for cell viability. Among these is the YycF (response regulator)-YycG (histidine kinase) system, which is highly conserved in and specific to the low-G+C content gram-positive bacteria. Given the pathogenic nature of several members of this class of bacteria, the YycF-YycG system has been suggested as a prime antimicrobial target. In an attempt to identify genes involved in regulation of this two-component system, a transposon mutagenesis study was designed to identify suppressors of a temperature-sensitive YycF mutant in Bacillus subtilis. Suppressors could be identified, and the prime target was the yycH gene located adjacent to yycG and within the same operon. A lacZ reporter assay revealed that YycF-regulated gene expression was elevated in a yycH strain, whereas disruption of any of the three downstream genes within the operon, yycI, yycJ, and yycK, showed no such effect. The concentrations of both YycG and YycF, assayed immunologically, remained unchanged between the wild-type and the yycH strain as determined by immunoassay. Alkaline phosphatase fusion studies showed that YycH is located external to the cell membrane, suggesting that it acts in the regulation of the sensor domain of the YycG sensor histidine kinase. The yycH strain showed a characteristic cell wall defect consistent with the previously suggested notion that the YycF-YycG system is involved in regulating cell wall homeostasis and indicating that either up- or down-regulation of YycF activity affects this homeostatic mechanism.
在细菌中发现的众多双组分信号转导系统中,只有极少数被证明对细胞存活至关重要。其中包括YycF(应答调节因子)-YycG(组氨酸激酶)系统,该系统在低G+C含量的革兰氏阳性细菌中高度保守且具有特异性。鉴于这类细菌中几个成员的致病特性,YycF-YycG系统被认为是主要的抗菌靶点。为了鉴定参与调节该双组分系统的基因,设计了一项转座子诱变研究,以鉴定枯草芽孢杆菌中温度敏感型YycF突变体的抑制子。可以鉴定出抑制子,主要靶点是位于yycG附近且在同一操纵子内的yycH基因。lacZ报告基因检测显示,在yycH菌株中YycF调节的基因表达升高,而操纵子内三个下游基因yycI、yycJ和yycK中的任何一个被破坏都没有这种效果。通过免疫测定法测定,野生型和yycH菌株之间免疫测定的YycG和YycF浓度均保持不变。碱性磷酸酶融合研究表明,YycH位于细胞膜外,表明它在调节YycG传感器组氨酸激酶的传感器结构域中起作用。yycH菌株表现出特征性的细胞壁缺陷,这与先前提出的YycF-YycG系统参与调节细胞壁稳态的观点一致,表明YycF活性的上调或下调都会影响这种稳态机制。