bayesReact:表达耦合调控图案分析检测癌症和单细胞水平的 microRNA 活性

Asta Mannstaedt Rasmussen, Alexandre Bouchard-Cote, Jakob Skou Pedersen
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摘要

研究动机:调控约束是维持组织和细胞完整性的关键,在发育过程和环境反应中发挥着重要作用。然而,许多调控机制在单细胞水平上仍未被观察到,在某些情况下,统计推断可能有助于阐明它们在疾病进展过程中的特异性活动和干扰。成果:我们介绍了bayesReact(BAYESian modeling of Regular Expression ACTivity),这是一种在实验排序序列中出现主题的生成模型,用于推断基于主题的调控活动。该方法针对微小 RNA(miRNA)进行了评估,miRNA 通过目标 mRNA 失稳和翻译抑制进行转录后调控。推断出的 miRNA 活性与癌症基因组图谱(TCGA)原发性肿瘤和小鼠干细胞中观察到的 miRNA 表达呈正相关。顶级 miRNA 活性图谱与顶级 miRNA 或 mRNA 表达图谱一样,都能为 TCGA 癌症类型集群鉴定提供信息。活性捕捉了在匹配表达中观察到的组织特异性 miRNA 模式,例如 miR-122-5p 在肝脏中的表达和 miR-124-3p 在低级别胶质瘤(LGG)中的表达。我们观察到这两种 miRNA 的活性与它们的靶基因表达之间存在负相关,包括 LGG 中 miR-124-3p 活性与抗神经元 REST 表达之间的负相关。在稀疏计数数据上,bayesReact 优于现有的 miReact 方法,而且与单细胞数据中 miRNA 表达的相关性更高。该方法恢复了小鼠干细胞分化过程中主要 miRNA 的时间活动,包括 miR-298-5p、miR-92-2-5p 和大型 Sfmbt2 簇(miR-297-669)。bayesReact 模型是一种概率模型,可量化所有估计值的不确定性。它是无监督的,允许对批量或单细胞数据进行筛选,以确定特定条件下的候选调控基因。它进一步改进了单细胞数据中的 miRNA 活性推断。可用性与实现:bayesReact 以 R 软件包的形式实现,使用 Hamiltonian Monte-Carlo 采样器进行后验近似,可在 https://github.com/astamr/bayesReact 上获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
bayesReact: Expression-coupled regulatory motif analysis detects microRNA activity in cancer and at the single cell level
Motivation: Regulatory constraints are crucial in maintaining tissue and cell integrity, and play important roles during developmental processes and environmental responses. Yet many regulatory mechanisms remain unobserved at the single-cell level and statistical inference may, in some cases, help elucidate their condition-specific activity and perturbation during disease progression. Results: We introduce bayesReact (BAYESian modeling of Regular Expression ACTivity), a generative model of motif occurrence across experimentally ranked sequences to infer motif-based regulatory activities. The method is evaluated for microRNAs (miRNAs), which perform post-transcriptional regulation through target mRNA destabilization and translational repression. Inferred miRNA activities positively correlate with the observed miRNA expressions in primary tumors from The Cancer Genome Atlas (TCGA) and mouse stem cells. The top miRNA activity profiles are as informative for TCGA cancer-type cluster identification as the top miRNA or mRNA expression profiles. The activity captures tissue-specific miRNA patterns observed in the matched expression, e.g., the expression of miR-122-5p in the liver and miR-124-3p in low-grade gliomas (LGG). We observe a negative association between the activity of the two miRNAs and their target gene expressions, including between the miR-124-3p activity and the anti-neuronal REST expression in LGG. bayesReact outperforms the existing method, miReact, on sparse count data, and shows a higher correlation with the miRNA expression in single-cell data. The method recovers temporal activities of prominent miRNAs during murine stem cell differentiation, including miR-298-5p, miR-92-2-5p, and the large Sfmbt2 cluster (miR-297-669). The bayesReact model is probabilistic and quantifies the uncertainty of all provided estimates. It is unsupervised and permits screens of bulk or single-cell data to identify condition-specific regulatory motif candidates. It further improves miRNA activity inference in single-cell data. Availability and implementation: bayesReact is implemented as an R-package, uses a Hamiltonian Monte-Carlo sampler for posterior approximation, and is available at https://github.com/astamr/bayesReact.
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