Liu Bing, Jiang Tianzi, Ma Songde, Zhao Huizhi, Li Jun, Jiang Xingpeng, Zhang Jing
National Laboratory of Pattern Recognition, Institute of Automation, Chinese Academy of Sciences, Beijing 100080, PR China.
Biochem Biophys Res Commun. 2006 Nov 3;349(4):1308-14. doi: 10.1016/j.bbrc.2006.08.168. Epub 2006 Sep 7.
It is believed that large numbers of genes are involved in common human brain diseases. Here, we propose a novel computational strategy for simultaneously identifying multiple candidate genes for genetic human brain diseases from a brain-specific gene network-level perspective. By integrating diverse genomic and proteomic datasets based on Bayesian statistical model, we built a large-scale human brain-specific gene network. Based on this network and minor prior knowledge of a specific brain disease, we can effectively identify multiple candidate genes for this disease. When four known Alzheimer's disease genes were used as the prior knowledge, among the top 46 high-scoring genes that we have found, 37 were previously reported to be associated with Alzheimer's disease. And the higher score a gene has, the more likely this gene is a disease-related one. The results suggest that the proposed method is effective, convenient, and applicable in the future genetic studies.
人们认为大量基因与常见的人类脑部疾病有关。在此,我们提出一种新颖的计算策略,从大脑特异性基因网络层面同时识别遗传性人类脑部疾病的多个候选基因。通过基于贝叶斯统计模型整合多样的基因组和蛋白质组数据集,我们构建了一个大规模的人类大脑特异性基因网络。基于这个网络以及某种特定脑部疾病的少量先验知识,我们能够有效地识别出该疾病的多个候选基因。当将四个已知的阿尔茨海默病基因用作先验知识时,在我们发现的前46个高分基因中,有37个先前已被报道与阿尔茨海默病相关。而且一个基因的分数越高,该基因与疾病相关的可能性就越大。结果表明所提出的方法是有效、便捷的,并且适用于未来的基因研究。