Singh Nitesh Kumar, Selvam S Mahalaxmi, Chakravarthy Paulsharma
S.R.M Institute of Science and Technology, Chennai, India.
In Silico Biol. 2006;6(6):485-93.
With the completion of the Human Genome Project in 2003, many new projects to sequence bacterial genomes were started and soon many complete bacterial genome sequences were available. The sequenced genomes of pathogenic bacteria provide useful information for understanding host-pathogen interactions. These data prove to be a new weapon in fighting against pathogenic bacteria by providing information about potential drug targets. But the limitation of computational tools for finding potential drug targets has hindered the process and further experimental analysis. There are many in silico approaches proposed for finding drug targets but only few have been automated. One such approach finds essential genes in bacterial genomes with no human homologue and predicts these as potential drug targets. The same approach is used in our tool. T-iDT, a tool for the identification of drug targets, finds essential genes by comparing a bacterial gene set against DEG (Database of Essential Genes) and excludes homologue genes by comparing against a human protein database. The tool predicts both the set of essential genes as well as potential target genes for the given genome. The tool was tested with Mycobacterium tuberculosis and results were validated. With default parameters, the tool predicted 236 essential genes and 52 genes to encode potential drug targets. A pathway-based approach was used to validate these potential drug target genes. The pathway in which the products of these genes are involved was determined. Our analysis shows that almost all these pathways are very essential for the bacterial survival and hence these genes encode possible drug targets. Our tool provides a fast method for finding possible drug targets in bacterial genomes with varying stringency level. The tool will be helpful in finding possible drug targets in various pathogenic organisms and can be used for further analysis in novel therapeutic drug development. The tool can be downloaded from http://www.milser.co.in/research.htm and http://www.srmbioinformatics.edu.in/ forum.htm.
随着2003年人类基因组计划的完成,许多新的细菌基因组测序项目启动,很快就有了许多完整的细菌基因组序列。病原菌的测序基因组为理解宿主与病原体的相互作用提供了有用信息。这些数据通过提供有关潜在药物靶点的信息,成为对抗病原菌的新武器。但用于寻找潜在药物靶点的计算工具的局限性阻碍了这一进程及进一步的实验分析。有许多计算机模拟方法被提出来寻找药物靶点,但只有少数实现了自动化。其中一种方法是在细菌基因组中寻找没有人类同源物的必需基因,并将其预测为潜在药物靶点。我们的工具使用的就是这种方法。T-iDT是一种药物靶点识别工具,它通过将细菌基因集与必需基因数据库(DEG)进行比较来找到必需基因,并通过与人类蛋白质数据库进行比较来排除同源基因。该工具能预测给定基因组的必需基因集以及潜在靶基因。该工具在结核分枝杆菌上进行了测试,结果得到了验证。在默认参数下,该工具预测了236个必需基因和52个编码潜在药物靶点的基因。采用基于通路的方法对这些潜在药物靶基因进行了验证。确定了这些基因产物所参与的通路。我们的分析表明,几乎所有这些通路对细菌的生存都非常重要,因此这些基因编码了可能的药物靶点。我们的工具提供了一种快速方法,可在不同严格程度下在细菌基因组中寻找可能的药物靶点。该工具将有助于在各种致病生物体中寻找可能的药物靶点,并可用于新型治疗药物开发的进一步分析。该工具可从http://www.milser.co.in/research.htm和http://www.srmbioinformatics.edu.in/forum.htm下载。