Yang C, Kaplan H B
Department of Microbiology and Molecular Genetics, University of Texas Medical School at Houston, 77030, USA.
J Bacteriol. 1997 Dec;179(24):7759-67. doi: 10.1128/jb.179.24.7759-7767.1997.
Initiation of Myxococcus xanthus multicellular development requires integration of information concerning the cells' nutrient status and density. A gain-of-function mutation, sasB7, that bypasses both the starvation and high cell density requirements for developmental expression of the 4521 reporter gene, maps to the sasS gene. The wild-type sasS gene was cloned and sequenced. This gene is predicted to encode a sensor histidine protein kinase that appears to be a key element in the transduction of starvation and cell density inputs. The sasS null mutants express 4521 at a basal level, form defective fruiting bodies, and exhibit reduced sporulation efficiencies. These data indicate that the wild-type sasS gene product functions as a positive regulator of 4521 expression and participates in M. xanthus development. The N terminus of SasS is predicted to contain two transmembrane domains that would locate the protein to the cytoplasmic membrane. The sasB7 mutation, an E139K missense mutation, maps to the predicted N-terminal periplasmic region. The C terminus of SasS contains all of the conserved residues typical of the sensor histidine protein kinases. SasS is predicted to be the sensor protein in a two-component system that integrates information required for M. xanthus developmental gene expression.
黄色粘球菌多细胞发育的起始需要整合有关细胞营养状态和密度的信息。一个功能获得性突变体sasB7,它能绕过饥饿和高细胞密度这两个4521报告基因发育表达所需的条件,该突变映射到sasS基因。野生型sasS基因被克隆并测序。该基因预计编码一种传感组氨酸蛋白激酶,它似乎是饥饿和细胞密度信号转导中的关键元件。sasS基因敲除突变体在基础水平表达4521,形成有缺陷的子实体,并表现出降低的孢子形成效率。这些数据表明野生型sasS基因产物作为4521表达的正调控因子,并参与黄色粘球菌的发育。SasS的N端预计包含两个跨膜结构域,这会将该蛋白定位到细胞质膜。sasB7突变是一个E139K错义突变,映射到预测的N端周质区域。SasS的C端包含传感组氨酸蛋白激酶所有典型的保守残基。SasS预计是一个双组分系统中的传感蛋白,该系统整合了黄色粘球菌发育基因表达所需的信息。