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信号通路项目,一个用于哺乳动物细胞信号通路的整合组学知识库。

The Signaling Pathways Project, an integrated 'omics knowledgebase for mammalian cellular signaling pathways.

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, 77030, USA.

Duncan NCI Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas, 77030, USA.

出版信息

Sci Data. 2019 Oct 31;6(1):252. doi: 10.1038/s41597-019-0193-4.

DOI:10.1038/s41597-019-0193-4
PMID:31672983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6823428/
Abstract

Mining of integrated public transcriptomic and ChIP-Seq (cistromic) datasets can illuminate functions of mammalian cellular signaling pathways not yet explored in the research literature. Here, we designed a web knowledgebase, the Signaling Pathways Project (SPP), which incorporates community classifications of signaling pathway nodes (receptors, enzymes, transcription factors and co-nodes) and their cognate bioactive small molecules. We then mapped over 10,000 public transcriptomic or cistromic experiments to their pathway node or biosample of study. To enable prediction of pathway node-gene target transcriptional regulatory relationships through SPP, we generated consensus 'omics signatures, or consensomes, which ranked genes based on measures of their significant differential expression or promoter occupancy across transcriptomic or cistromic experiments mapped to a specific node family. Consensomes were validated using alignment with canonical literature knowledge, gene target-level integration of transcriptomic and cistromic data points, and in bench experiments confirming previously uncharacterized node-gene target regulatory relationships. To expose the SPP knowledgebase to researchers, a web browser interface was designed that accommodates numerous routine data mining strategies. SPP is freely accessible at https://www.signalingpathways.org .

摘要

整合公共转录组学和 ChIP-Seq(染色质)数据集的挖掘可以阐明哺乳动物细胞信号通路的功能,这些功能在研究文献中尚未得到探索。在这里,我们设计了一个网络知识库,即信号通路项目(SPP),其中包含信号通路节点(受体、酶、转录因子和共节点)及其同源生物活性小分子的社区分类。然后,我们将超过 10000 个公共转录组学或染色质实验映射到它们的通路节点或研究的生物样本。为了能够通过 SPP 预测通路节点-基因的转录调控关系,我们生成了共识“组学”特征,或 consensomes,根据它们在特定节点家族映射的转录组学或染色质实验中显著差异表达或启动子占据的衡量标准,对基因进行排序。通过与规范文献知识的对齐、转录组学和染色质数据点的基因靶向水平整合以及在确认先前未表征的节点-基因靶向调控关系的基准实验中验证了 consensomes。为了向研究人员展示 SPP 知识库,我们设计了一个网络浏览器界面,该界面可适应许多常规的数据挖掘策略。SPP 可在 https://www.signalingpathways.org 免费获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/95b41939c722/41597_2019_193_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/2d4927259e01/41597_2019_193_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/950f0eff448f/41597_2019_193_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/2dcddec30746/41597_2019_193_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/26d74018f19b/41597_2019_193_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/10087b07951c/41597_2019_193_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/0c20ee17dcfa/41597_2019_193_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/95b41939c722/41597_2019_193_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/2d4927259e01/41597_2019_193_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/950f0eff448f/41597_2019_193_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/2dcddec30746/41597_2019_193_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/26d74018f19b/41597_2019_193_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/10087b07951c/41597_2019_193_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/0c20ee17dcfa/41597_2019_193_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b41/6823428/95b41939c722/41597_2019_193_Fig7_HTML.jpg

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