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系统分析组织和细胞表型中活跃转录的核心基质基因。

Systematic Analysis of Actively Transcribed Core Matrisome Genes Across Tissues and Cell Phenotypes.

机构信息

Department of Diagnostic & Biomedical Sciences, University of Texas Health Science Center at Houston School of Dentistry, 1941 East Road, BBS-4220, Houston, TX 77054, USA.

Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, P.O. Box 301402 Houston, TX 77230, USA.

出版信息

Matrix Biol. 2022 Aug;111:95-107. doi: 10.1016/j.matbio.2022.06.003. Epub 2022 Jun 14.

Abstract

The extracellular matrix (ECM) is a highly dynamic, well-organized acellular network of tissue-specific biomolecules, that can be divided into structural or core ECM proteins and ECM-associated proteins. The ECM serves as a blueprint for organ development and function and, when structurally altered through mutation, altered expression, or degradation, can lead to debilitating syndromes that often affect one tissue more than another. Cross-referencing the FANTOM5 SSTAR (Semantic catalog of Samples, Transcription initiation And Regulators) and the defined catalog of core matrisome ECM (glyco)proteins, we conducted a comprehensive analysis of 511 different human samples to annotate the context-specific transcription of the individual components of the defined matrisome. Relative log expression normalized SSTAR cap analysis gene expression peak data files were downloaded from the FANTOM5 online database and filtered to exclude all cell lines and diseased tissues. Promoter-level expression values were categorized further into eight core tissue systems and three major ECM categories: proteoglycans, glycoproteins, and collagens. Hierarchical clustering and correlation analyses were conducted to identify complex relationships in promoter-driven gene expression activity. Integration of the core matrisome and curated FANTOM5 SSTAR data creates a unique tool that provides insight into the promoter-level expression of ECM-encoding genes in a tissue- and cell-specific manner. Unbiased clustering of cap analysis gene expression peak data reveals unique ECM signatures within defined tissue systems. Correlation analysis among tissue systems exposes both positive and negative correlation of ECM promoters with varying levels of significance. This tool can be used to provide new insight into the relationships between ECM components and tissues and can inform future research on the ECM in human disease and development. We invite the matrix biology community to continue to explore and discuss this dataset as part of a larger and continuing conversation about the human ECM. An interactive web tool can be found at matrixpromoterome.github.io along with additional resources that can be found at dx.doi.org/10.6084/m9.figshare.19794481 (figures) and https://figshare.com/s/e18ecbc3ae5aaf919b78 (python notebook).

摘要

细胞外基质 (ECM) 是一种高度动态、组织特异性生物分子的良好组织化无细胞网络,可分为结构性或核心 ECM 蛋白和 ECM 相关蛋白。ECM 是器官发育和功能的蓝图,当通过突变、改变表达或降解而在结构上改变时,可能导致衰弱综合征,这些综合征通常更多地影响一种组织而不是另一种组织。我们交叉参考了 FANTOM5 SSTAR(样本、转录起始和调节剂的语义目录)和定义的核心基质 ECM(糖基)蛋白目录,对 511 个人类样本进行了全面分析,以注释定义的基质中各个成分的特定转录。从 FANTOM5 在线数据库下载相对对数表达标准化 SSTAR 帽分析基因表达峰数据文件,并进行过滤以排除所有细胞系和患病组织。启动子水平表达值进一步分为八个核心组织系统和三个主要 ECM 类别:蛋白聚糖、糖蛋白和胶原蛋白。进行层次聚类和相关性分析,以识别启动子驱动基因表达活性中的复杂关系。核心基质和经过精心整理的 FANTOM5 SSTAR 数据的整合创建了一个独特的工具,可深入了解 ECM 编码基因在组织和细胞特异性方式下的启动子水平表达。无偏聚类帽分析基因表达峰数据揭示了定义组织系统内独特的 ECM 特征。组织系统之间的相关性分析揭示了 ECM 启动子与不同显著性水平的正相关和负相关。该工具可用于提供有关 ECM 成分与组织之间关系的新见解,并为人类疾病和发育中 ECM 的未来研究提供信息。我们邀请基质生物学界继续探索和讨论这个数据集,作为关于人类 ECM 的更大和持续对话的一部分。交互式网络工具可在 matrixpromoterome.github.io 上找到,此外还有其他资源可在 dx.doi.org/10.6084/m9.figshare.19794481(图)和 https://figshare.com/s/e18ecbc3ae5aaf919b78(python 笔记本)上找到。

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