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Genome-wide analysis of yeast expression data based on a priori generated co-regulation cliques

机译:基于先验产生的共调控集团的酵母表达数据的全基因组分析

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摘要

DNA microarrays are highly sensitive tools to evaluate the gene expression status of organismic samples and standardized array formats exist for many different sample types. Differential expression studies usually utilize the strongest upor downregulated genes to generate networks visualizing the relationships among these genes. To include all yeast genes in one analysis and to get broader information on all cellular responses, we test a priori input of predefined genome-wide expression cliques and subsequent statistical analysis of the expression data. To this end, we generate a set of 72 co-regulation cliques using the information from 3196 microarray experiments. The obtained cliques performed highly significant in gene ontology and transcription factor enrichment analyses. We then tested the clique set on individual microarray experiments reporting on responses to pheromone, glycerol versus glucose based growth and the cellular response to heat. In all cases a highly significant determination of affected expression cliques was possible based on their average expression differences, the positions of their genes within hit rankings (UpRegScore) or the enrichment of the Top200 hits in certain cliques. The 72 cliques were finally used to compare experiments, which reported on the transcriptional response to polyglutamine proteins of different lengths. Using the predefined clique set it is possible to identify with high sensitivity and good significance sample and condition specific changes to gene expression. We thus conclude that an analysis, starting with these 72 preformed expression cliques, can complement traditional microarray analyses by visualizing the entire response on a static genome-wide gene set.
机译:DNA微阵列是用于评估生物样品基因表达状态的高度敏感的工具,并且存在许多不同样品类型的标准化阵列格式。差异表达研究通常利用最强的上调或下调基因来生成可视化这些基因之间关系的网络。为了将所有酵母基因包括在一项分析中并获得所有细胞应答的更广泛信息,我们测试了预先定义的全基因组表达集团的先验输入以及随后的表达数据统计分析。为此,我们使用来自3196个微阵列实验的信息生成了72个共同调控集团。获得的集团在基因本体论和转录因子富集分析中表现出非常重要的意义。然后,我们在单个微阵列实验中测试了该系统,该实验报告了对信息素,甘油对葡萄糖的响应以及基于葡萄糖的生长以及对热的细胞响应。在所有情况下,都可以根据受影响的表达群体的平均表达差异,其基因在命中排名中的位置(UpRegScore)或某些群体中Top200命中的富集来高度确定。最终将这72个小组用于比较实验,该实验报道了对不同长度的聚谷氨酰胺蛋白的转录反应。使用预定义的集团集,可以以高灵敏度和高显着性鉴定样品,并调节基因表达的特异性变化。因此,我们得出的结论是,从这72个预先形成的表达群体开始的分析可以通过可视化整个静态全基因组基因集上的整个响应来补充传统的微阵列分析。

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