Hecker M, Engelmann S
Ernst-Moritz-Arndt Universität, Institut für Mikrobiologie, Greifswald, Germany.
Int J Med Microbiol. 2000 May;290(2):123-34. doi: 10.1016/S1438-4221(00)80080-6.
The complete sequence of the bacterial genomes provides new perspectives for the study of gene expression and gene function. By the combination of the highly sensitive 2-dimensional (2D) protein gel electrophoresis with the identification of the protein spots by microsequencing or mass spectrometry we established a 2D protein index of Bacillus subtilis that currently comprises almost 400 protein entries. A computer-aided evaluation of the 2D gels loaded with radioactively-labelled proteins from growing or stressed/starved cells proved to be a powerful tool in the analysis of global regulation of the expression of the entire genome. For the general stress regulon it is demonstrated how the proteomics approach can be used to analyse the regulation, structure and function of still unknown regulons. The application of this approach is illustrated for the sigmaB dependent general stress regulon. For the comprehensive description of proteins/genes belonging to stimulons or regulons it is generally recommended to complement the proteome approach with DNA array techniques in order to identify and allocate still undiscovered members of individual regulons. This approach is also very attractive to uncover the function of still unknown global regulators and regulons and to dissect the entire genome into its basic modules of global regulation. The same strategy can be used to analyse the regulation, structure and function of regulons encoding virulence factors of pathogenic bacteria for a comprehensive understanding of the pathogenicity and for the identification of new antibacterial targets.
细菌基因组的完整序列为基因表达和基因功能的研究提供了新的视角。通过将高灵敏度的二维(2D)蛋白质凝胶电泳与通过微量测序或质谱法对蛋白质斑点进行鉴定相结合,我们建立了枯草芽孢杆菌的二维蛋白质索引,目前该索引包含近400个蛋白质条目。对加载有来自生长或应激/饥饿细胞的放射性标记蛋白质的二维凝胶进行计算机辅助评估,被证明是分析整个基因组表达全局调控的有力工具。对于一般应激调节子,展示了蛋白质组学方法如何用于分析仍然未知的调节子的调控、结构和功能。以依赖于σB的一般应激调节子为例说明了该方法的应用。为了全面描述属于刺激子或调节子的蛋白质/基因,通常建议用DNA阵列技术补充蛋白质组学方法,以便识别和定位各个调节子中尚未发现的成员。这种方法对于揭示仍然未知的全局调节因子和调节子的功能,以及将整个基因组分解为其全局调节的基本模块也非常有吸引力。同样的策略可用于分析编码病原菌毒力因子的调节子的调控、结构和功能,以全面了解致病性并鉴定新的抗菌靶点。