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Computationally Identifying Novel NF-κB-Regulated Immune Genes in the Human Genome

机译:计算鉴定人类基因组中新的NF-κB调控的免疫基因

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摘要

Identifying novel NF-κB-regulated immune genes in the human genome is important to our understanding of immune mechanisms and immune diseases. We fit logistic regression models to the promoters of 62 known NF-κB-regulated immune genes, to find patterns of transcription factor binding in the promoters of genes with known immune function. Using these patterns, we scanned the promoters of additional genes to find matches to the patterns, selected those with NF-κB binding sites conserved in the mouse or fly, and then confirmed them as NF-κB-regulated immune genes based on expression data. Among 6440 previously identified promoters in the human genome, we found 28 predicted immune gene promoters, 19 of which regulate genes with known function, allowing us to calculate specificity of 93%–100% for the method. We calculated sensitivity of 42% when searching the 62 known immune gene promoters. We found nine novel NF-κB-regulated immune genes which are consistent with available SAGE data. Our method of predicting gene function, based on characteristic patterns of transcription factor binding, evolutionary conservation, and expression studies, would be applicable to finding genes with other functions.
机译:鉴定人类基因组中新的由NF-κB调节的免疫基因对于我们对免疫机制和免疫疾病的理解很重要。我们将逻辑回归模型与62个已知NF-κB调节的免疫基因的启动子拟合,以发现具有已知免疫功能的基因的启动子中转录因子结合的模式。使用这些模式,我们扫描了其他基因的启动子以找到与该模式的匹配,选择了在小鼠或果蝇中具有NF-κB结合位点的保守位点,然后基于表达数据将其确认为NF-κB调控的免疫基因。在人类基因组中先前确定的6440个启动子中,我们发现了28个预测的免疫基因启动子,其中19个调节功能已知的基因,这使我们能够计算该方法的特异性为93%–100%。搜索62个已知的免疫基因启动子时,我们计算出的敏感性为42%。我们发现了九个新的NF-κB调节的免疫基因,与可用的SAGE数据一致。基于转录因子结合,进化保守和表达研究的特征模式,我们预测基因功能的方法将适用于寻找具有其他功能的基因。

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