Zhou Xinyuan, Qin Yanxia, Li Jiangxue, Fan Linyuan, Zhang Shun, Zhang Bing, Wu Luoxuan, Gao Anwei, Yang Yongsan, Lv Xueqin, Guo Bingzhou, Sun Liang
Binzhou People's Hospital Affiliated to Shandong First Medical University/College of Medical Information and Artificial Intelligence, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong 250117, China.
Institute of Brain Science and Brain-inspired Research, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong 250117, China.
Nucleic Acids Res. 2025 Jan 6;53(D1):D468-D476. doi: 10.1093/nar/gkae905.
Long non-coding RNAs were commonly viewed as non-coding elements. However, they are increasingly recognized for their ability to be translated into proteins, thereby playing a significant role in various cellular processes and diseases. With developments in biotechnology and computational algorithms, a range of novel approaches are being applied to investigate the translation of long non-coding RNA (lncRNAs). Herein, we developed the LncPepAtlas database (http://www.cnitbiotool.net/LncPepAtlas/), which aims to compile multiple evidences for the translation of lncRNAs and annotations for the upstream regulation of lncRNAs across various species. LncPepAtlas integrated compelling evidence from nine distinct sources for the translation of lncRNAs. These include a dataset comprising 2631 publicly available Ribo-seq samples from nine species, which has been collected and analysed. LncPepAtlas offers extensive annotation for lncRNA upstream regulation and expression profiles across various cancers, tissues or cell lines at transcriptional and translational levels. Importantly, it enables novel antigen predictions for lncRNA-encoded peptides. By identifying numerous peptide candidates that could potentially bind to major histocompatibility complex class I and II molecules, this work may provide new insights into cancer immunotherapy. The function of peptides were inferred by aligning them with experimentally detected proteins. LncPepAtlas aims to become a convenient resource for exploring translatable lncRNAs.
长链非编码RNA通常被视为非编码元件。然而,它们越来越被认为具有翻译成蛋白质的能力,从而在各种细胞过程和疾病中发挥重要作用。随着生物技术和计算算法的发展,一系列新颖的方法正被应用于研究长链非编码RNA(lncRNAs)的翻译。在此,我们开发了LncPepAtlas数据库(http://www.cnitbiotool.net/LncPepAtlas/),其旨在汇集lncRNAs翻译的多种证据以及跨物种lncRNAs上游调控的注释。LncPepAtlas整合了来自九个不同来源的关于lncRNAs翻译的有力证据。这些包括一个由来自九个物种的2631个公开可用的核糖体图谱样本组成的数据集,该数据集已被收集和分析。LncPepAtlas在转录和翻译水平上提供了关于各种癌症、组织或细胞系中lncRNA上游调控和表达谱的广泛注释。重要的是,它能够对lncRNA编码的肽进行新抗原预测。通过识别众多可能与主要组织相容性复合体I类和II类分子结合的肽候选物,这项工作可能为癌症免疫治疗提供新的见解。通过将肽与实验检测到的蛋白质进行比对来推断肽的功能。LncPepAtlas旨在成为探索可翻译lncRNAs的便利资源。