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3044条人类分子通路组成成分功能角色的算法注释

Algorithmic Annotation of Functional Roles for Components of 3,044 Human Molecular Pathways.

作者信息

Sorokin Maxim, Borisov Nicolas, Kuzmin Denis, Gudkov Alexander, Zolotovskaia Marianna, Garazha Andrew, Buzdin Anton

机构信息

Omicsway Corp., Walnut, CA, United States.

Laboratory of Clinical Genomic Bioinformatics, I.M. Sechenov First Moscow State Medical University, Moscow, Russia.

出版信息

Front Genet. 2021 Feb 9;12:617059. doi: 10.3389/fgene.2021.617059. eCollection 2021.

Abstract

Current methods of high-throughput molecular and genomic analyses enabled to reconstruct thousands of human molecular pathways. Knowledge of molecular pathways structure and architecture taken along with the gene expression data can help interrogating the pathway activation levels (PALs) using different bioinformatic algorithms. In turn, the pathway activation profiles can characterize molecular processes, which are differentially regulated and give numeric characteristics of the extent of their activation or inhibition. However, different pathway nodes may have different functions toward overall pathway regulation, and calculation of PAL requires knowledge of molecular function of every node in the pathway in terms of its activator or inhibitory role. Thus, high-throughput annotation of functional roles of pathway nodes is required for the comprehensive analysis of the pathway activation profiles. We proposed an algorithm that identifies functional roles of the pathway components and applied it to annotate 3,044 human molecular pathways extracted from the Biocarta, Reactome, KEGG, Qiagen Pathway Central, NCI, and HumanCYC databases and including 9,022 gene products. The resulting knowledgebase can be applied for the direct calculation of the PALs and establishing large scale profiles of the signaling, metabolic, and DNA repair pathway regulation using high throughput gene expression data. We also provide a bioinformatic tool for PAL data calculations using the current pathway knowledgebase.

摘要

当前的高通量分子和基因组分析方法能够重建数千条人类分子通路。结合基因表达数据了解分子通路的结构和架构,有助于使用不同的生物信息学算法来探究通路激活水平(PAL)。反过来,通路激活谱可以表征分子过程,这些过程受到差异调节,并给出其激活或抑制程度的数值特征。然而,不同的通路节点对整体通路调节可能具有不同的功能,计算PAL需要了解通路中每个节点在其激活或抑制作用方面的分子功能。因此,为了全面分析通路激活谱,需要对通路节点的功能作用进行高通量注释。我们提出了一种算法,该算法可识别通路成分的功能作用,并将其应用于注释从Biocarta、Reactome、KEGG、Qiagen Pathway Central、NCI和HumanCYC数据库中提取的3044条人类分子通路,这些通路包含9022个基因产物。所得知识库可用于直接计算PAL,并利用高通量基因表达数据建立信号传导、代谢和DNA修复通路调节的大规模图谱。我们还提供了一个生物信息学工具,用于使用当前的通路知识库进行PAL数据计算。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08d5/7900570/f1a398d9c1c8/fgene-12-617059-g001.jpg

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