Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), University Medical Center Mainz, 55131 Mainz, Germany.
Center for Thrombosis and Hemostasis (CTH), University Medical Center Mainz, 55131 Mainz, Germany.
Nucleic Acids Res. 2021 Jan 8;49(D1):D243-D253. doi: 10.1093/nar/gkaa722.
Alternative polyadenylation (APA) profoundly expands the transcriptome complexity. Perturbations of APA can disrupt biological processes, ultimately resulting in devastating disorders. A major challenge in identifying mechanisms and consequences of APA (and its perturbations) lies in the complexity of RNA 3' end processing, involving poorly conserved RNA motifs and multi-component complexes consisting of far more than 50 proteins. This is further complicated in that RNA 3' end maturation is closely linked to transcription, RNA processing and even epigenetic (histone/DNA/RNA) modifications. Here, we present TREND-DB (http://shiny.imbei.uni-mainz.de:3838/trend-db), a resource cataloging the dynamic landscape of APA after depletion of >170 proteins involved in various facets of transcriptional, co- and post-transcriptional gene regulation, epigenetic modifications and further processes. TREND-DB visualizes the dynamics of transcriptome 3' end diversification (TREND) in a highly interactive manner; it provides a global APA network map and allows interrogating genes affected by specific APA-regulators and vice versa. It also permits condition-specific functional enrichment analyses of APA-affected genes, which suggest wide biological and clinical relevance across all RNAi conditions. The implementation of the UCSC Genome Browser provides additional customizable layers of gene regulation accounting for individual transcript isoforms (e.g. epigenetics, miRNA-binding sites and RNA-binding proteins). TREND-DB thereby fosters disentangling the role of APA for various biological programs, including potential disease mechanisms, and helps identify their diagnostic and therapeutic potential.
可变多聚腺苷酸化 (APA) 极大地扩展了转录组的复杂性。APA 的扰动会破坏生物过程,最终导致严重的疾病。识别 APA 的机制和后果 (及其扰动) 的主要挑战在于 RNA 3' 端加工的复杂性,涉及到保守性差的 RNA 基序和由 50 多种蛋白质组成的多成分复合物。此外,RNA 3' 端成熟与转录、RNA 处理甚至表观遗传 (组蛋白/DNA/RNA) 修饰密切相关,这使得情况更加复杂。在这里,我们展示了 TREND-DB(http://shiny.imbei.uni-mainz.de:3838/trend-db),这是一个资源目录,记录了在参与转录、共转录和转录后基因调控、表观遗传修饰和其他过程的 >170 种蛋白质耗尽后,APA 的动态景观。TREND-DB 以高度交互的方式可视化转录组 3' 端多样化的动态 (TREND);它提供了一个全局的 APA 网络图谱,并允许查询受特定 APA 调节剂影响的基因,反之亦然。它还允许对受 APA 影响的基因进行特定条件下的功能富集分析,这些分析表明在所有 RNAi 条件下都具有广泛的生物学和临床相关性。UCSC 基因组浏览器的实现提供了额外的可定制的基因调控层,用于个体转录本异构体 (例如,表观遗传学、miRNA 结合位点和 RNA 结合蛋白)。TREND-DB 有助于理清 APA 在各种生物学程序中的作用,包括潜在的疾病机制,并有助于识别它们的诊断和治疗潜力。