Smith Andrew D, Sumazin Pavel, Zhang Michael Q
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Mol Syst Biol. 2007;3:73. doi: 10.1038/msb4100114. Epub 2007 Jan 16.
Transcription factor-binding sites and the cis-regulatory modules they compose are central determinants of gene expression. We previously showed that binding site motifs and modules in proximal promoters can be used to predict a significant portion of mammalian tissue-specific transcription. Here, we report on a systematic analysis of promoters controlling tissue-specific expression in heart, kidney, liver, pancreas, skeletal muscle, testis and CD4 T cells, for both human and mouse. We integrated multiple sources of expression data to compile sets of transcripts with strong evidence for tissue-specific regulation. The analysis of the promoters corresponding to these sets produced a catalog of predicted tissue-specific motifs and modules, and cis-regulatory elements. Predicted regulatory interactions are supported by statistical evidence, and provide a foundation for targeted experiments that will improve our understanding of tissue-specific regulatory networks. In a broader context, methods used to construct the catalog provide a model for the analysis of genomic regions that regulate differentially expressed genes.
转录因子结合位点及其组成的顺式调控模块是基因表达的核心决定因素。我们之前表明,近端启动子中的结合位点基序和模块可用于预测相当一部分哺乳动物组织特异性转录。在此,我们报告了对人和小鼠心脏、肾脏、肝脏、胰腺、骨骼肌、睾丸及CD4 T细胞中控制组织特异性表达的启动子进行的系统分析。我们整合了多种表达数据来源,以编制具有组织特异性调控有力证据的转录本集合。对与这些集合相对应的启动子进行分析,生成了一个预测的组织特异性基序、模块和顺式调控元件目录。预测的调控相互作用得到了统计证据的支持,并为有针对性的实验提供了基础,这些实验将增进我们对组织特异性调控网络的理解。在更广泛的背景下,用于构建该目录的方法为分析调控差异表达基因的基因组区域提供了一个模型。