Single-cell network biology enabling cell-type-resolved disease genetics.

Junha Cha, Insuk Lee
{"title":"Single-cell network biology enabling cell-type-resolved disease genetics.","authors":"Junha Cha, Insuk Lee","doi":"10.1186/s44342-025-00042-7","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":94288,"journal":{"name":"Genomics & informatics","volume":"23 1","pages":"10"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11951680/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genomics & informatics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s44342-025-00042-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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、疾病基因和各种生物功能的遗传机制。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释,而这是仅由生物体级样本组成的数据集无法实现的。单细胞 RNA 测序(scRNA-seq)技术可通过计算区分细胞状态,为了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,丰富的细胞样本及其转录组全貌可以建立系统细胞类型特异性基因网络(CGN)模型,从而深入了解基因-细胞-疾病之间的关系。在这篇综述中,我们介绍了我们最近利用 scRNA-seq 数据集开发的基于参考和全新推断的基因功能相互作用网络。我们还介绍了 CGN 简编,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将成为绘制基因-细胞-疾病轴的关键方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信