Cha Junha, Lee Insuk
Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, 03722, Republic of Korea.
Genomics Inform. 2025 Mar 27;23(1):10. doi: 10.1186/s44342-025-00042-7.
Gene network models provide a foundation for graph theory approaches, aiding in the novel discovery of drug targets, disease genes, and genetic mechanisms for various biological functions. Disease genetics must be interpreted within the cellular context of disease-associated cell types, which cannot be achieved with datasets consisting solely of organism-level samples. Single-cell RNA sequencing (scRNA-seq) technology allows computational distinction of cell states which provides a unique opportunity to understand cellular biology that drives disease processes. Importantly, the abundance of cell samples with their transcriptome-wide profile allows the modeling of systemic cell-type-specific gene networks (CGNs), offering insights into gene-cell-disease relationships. In this review, we present reference-based and de novo inference of gene functional interaction networks that we have recently developed using scRNA-seq datasets. We also introduce a compendium of CGNs as a useful resource for cell-type-resolved disease genetics. By leveraging these advances, we envision single-cell network biology as the key approach for mapping the gene-cell-disease axis.
基因网络模型为图论方法提供了基础,有助于发现新的药物靶点、疾病基因以及各种生物学功能的遗传机制。疾病遗传学必须在与疾病相关的细胞类型的细胞背景下进行解读,而仅由生物体水平样本组成的数据集无法做到这一点。单细胞RNA测序(scRNA-seq)技术能够在计算上区分细胞状态,这为理解驱动疾病进程的细胞生物学提供了独特的机会。重要的是,大量具有全转录组概况的细胞样本能够对系统性细胞类型特异性基因网络(CGNs)进行建模,从而深入了解基因-细胞-疾病之间的关系。在本综述中,我们展示了基于参考和从头推断的基因功能相互作用网络,这些网络是我们最近利用scRNA-seq数据集开发的。我们还介绍了CGNs汇编,作为细胞类型解析疾病遗传学的有用资源。通过利用这些进展,我们设想单细胞网络生物学是绘制基因-细胞-疾病轴的关键方法。