Gao Shang, Dai Yang, Rehman Jalees
Department of Bioengineering, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
Department of Medicine, Division of Cardiology, University of Illinois at Chicago, Chicago, Illinois 60612, USA.
Genome Res. 2021 Jul;31(7):1296-1311. doi: 10.1101/gr.265595.120.
Single-cell RNA sequencing (scRNA-seq) has emerged as a powerful experimental approach to study cellular heterogeneity. One of the challenges in scRNA-seq data analysis is integrating different types of biological data to consistently recognize discrete biological functions and regulatory mechanisms of cells, such as transcription factor activities and gene regulatory networks in distinct cell populations. We have developed an approach to infer transcription factor activities from scRNA-seq data that leverages existing biological data on transcription factor binding sites. The Bayesian inference transcription factor activity model (BITFAM) integrates ChIP-seq transcription factor binding information into scRNA-seq data analysis. We show that the inferred transcription factor activities for key cell types identify regulatory transcription factors that are known to mechanistically control cell function and cell fate. The BITFAM approach not only identifies biologically meaningful transcription factor activities, but also provides valuable insights into underlying transcription factor regulatory mechanisms.
单细胞RNA测序(scRNA-seq)已成为研究细胞异质性的一种强大实验方法。scRNA-seq数据分析中的挑战之一是整合不同类型的生物学数据,以一致地识别细胞的离散生物学功能和调控机制,例如不同细胞群体中的转录因子活性和基因调控网络。我们开发了一种从scRNA-seq数据推断转录因子活性的方法,该方法利用了关于转录因子结合位点的现有生物学数据。贝叶斯推断转录因子活性模型(BITFAM)将ChIP-seq转录因子结合信息整合到scRNA-seq数据分析中。我们表明,针对关键细胞类型推断出的转录因子活性可识别已知在机制上控制细胞功能和细胞命运的调控转录因子。BITFAM方法不仅能识别具有生物学意义的转录因子活性,还能为潜在的转录因子调控机制提供有价值的见解。