Department of Basic Research, Guangzhou Laboratory, Guangzhou 510005, China.
Joint School of Life Sciences, Guangzhou Medical University and Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 511436, China.
Yi Chuan. 2024 Oct;46(10):795-806. doi: 10.16288/j.yczz.24-162.
Expression quantitative trait loci (eQTL) represent genetic variants that regulate gene expression levels. eQTL analysis has become a crucial method for identifying the functional roles of disease-associated genetic variants in the post-genome-wide association study (GWAS) era, yielding numerous significant discoveries. Traditional eQTL analysis relies on whole-genome sequencing combined with bulk RNA-seq, which obscures gene expression differences between cells and thus fails to identify cell type- or state-dependent eQTL. This limitation makes it challenging to elucidate the roles of disease-associated genetic variants under specific conditions. In recent years, with the development and widespread application of single-cell RNA sequencing (scRNA-seq) technology, scRNA-seq-based eQTL (sc-eQTL) research has emerged as a focal point. The advantage of this approach lies in its ability to leverage the resolution and granularity of single-cell sequencing to uncover eQTL that are dependent on cell type, cell state, and cellular dynamics. This significantly enhances our ability to analyze genetic variants associated with gene expression. Consequently, it holds substantial significance for advancing our understanding of the formation of complex organs and the mechanisms underlying disease onset, progression, intervention, and treatment. This review comprehensively examines the recent advancements in sc-eQTL studies, focusing on their development, experimental design strategies, modeling approaches, and current challenges. The aim is to offer researchers novel perspectives for identifying disease-associated loci and elucidating gene regulatory mechanisms.
表达数量性状基因座(eQTL)代表调节基因表达水平的遗传变异。eQTL 分析已成为在后全基因组关联研究(GWAS)时代识别与疾病相关的遗传变异的功能作用的关键方法,产生了许多重要的发现。传统的 eQTL 分析依赖于全基因组测序与批量 RNA-seq 的结合,这掩盖了细胞之间的基因表达差异,因此无法识别细胞类型或状态依赖的 eQTL。这种局限性使得阐明特定条件下与疾病相关的遗传变异的作用变得具有挑战性。近年来,随着单细胞 RNA 测序(scRNA-seq)技术的发展和广泛应用,基于 scRNA-seq 的 eQTL(sc-eQTL)研究已成为焦点。这种方法的优势在于它能够利用单细胞测序的分辨率和粒度来揭示依赖于细胞类型、细胞状态和细胞动态的 eQTL。这极大地增强了我们分析与基因表达相关的遗传变异的能力。因此,它对于推进我们对复杂器官形成和疾病发生、发展、干预和治疗机制的理解具有重要意义。本综述全面考察了 sc-eQTL 研究的最新进展,重点介绍了它们的发展、实验设计策略、建模方法和当前的挑战。目的是为研究人员提供识别与疾病相关的基因座和阐明基因调控机制的新视角。