时间基因地形:通过动态基因表达可视化推进精准医疗。

IF 3.9 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in bioinformatics Pub Date : 2025-06-18 eCollection Date: 2025-01-01 DOI:10.3389/fbinf.2025.1602850
Ehsan Saghapour, Rahul Sharma, Delower Hossain, Kevin Song, Zhandos Sembay, Jake Y Chen
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引用次数: 0

摘要

了解基因表达的时间动态对于解释生物反应至关重要,特别是在药物治疗研究中。传统的可视化技术,如热图和静态聚类,往往不能有效地捕捉这些时间动态,特别是在分析大规模多维数据集时。这些传统的方法往往模糊了细粒度的时间转换,导致过度的可视化,清晰度降低,以及生物重要模式的有限可解释性。方法:为了解决这些可视化挑战,我们引入了Temporal GeneTerrain,这是一种先进的方法,旨在表示基因表达随时间的动态变化。利用GSE149428数据集(0、3、6、9、12和24小时),我们应用Temporal GeneTerrain比较甲氟喹(M)、他莫昔芬(T)和withaferin A (W)单独、全两两组合和三联组合(TM、TW、MW和TMW)在LNCaP前列腺癌细胞中诱导的转录组扰动。首先对表达值进行Z-score归一化,选出1000个最易表达的基因。为了确保协调的时间动态,我们计算了这些基因之间的Pearson相关系数,并保留了r≥0.5的基因,得到了999个强共表达候选基因。然后,我们为这些基因构建了一个蛋白质-蛋白质相互作用网络,并使用Kamada-Kawai力导向算法将其嵌入二维中。最后,对于每个时间点和处理,我们将对应基因的归一化表达值映射到固定的Kamada-Kawai布局上,作为高斯密度场(σ = 0.03),为每个时间条件组合生成不同的Temporal GeneTerrain map。结果:Temporal GeneTerrain的应用揭示了基因表达的复杂时间变化,特别是揭示了ngf刺激转录和联合药物治疗下未折叠蛋白反应等途径的延迟反应。与传统的热图可视化相比,Temporal GeneTerrain显著提高了分辨率和可解释性,有效地捕获了基因表达模式的多维性和瞬态性。这一改进为进一步的研究和分析提供了坚实的基础,保证了科学界对该方法的可靠性。讨论:Temporal GeneTerrain通过提供基因表达动态的直观和详细的表示来解决传统可视化方法的局限性。与热图和静态聚类等其他方法相比,Temporal GeneTerrain独特地捕捉了基因表达模式的瞬态性质。该方法显著提高了复杂生物数据集的可解释性,从而支持生物研究和治疗开发中的明智决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Temporal GeneTerrain: advancing precision medicine through dynamic gene expression visualization.

Introduction: Understanding the temporal dynamics of gene expression is vital for interpreting biological responses, especially in drug treatment studies. Conventional visualization techniques, such as heatmaps and static clustering, often fail to effectively capture these temporal dynamics, particularly when analyzing large-scale multidimensional datasets. These traditional methods tend to obscure fine-grained temporal transitions, resulting in overcrowded visualizations, diminished clarity, and limited interpretability of biologically significant patterns.

Methods: To address these visualization challenges, we introduce Temporal GeneTerrain, an advanced method designed to represent dynamic changes in gene expression over time. We applied Temporal GeneTerrain to compare transcriptomic perturbations induced by mefloquine (M), tamoxifen (T), and withaferin A (W), both individually and in all-pairwise and triple combinations (TM, TW, MW, and TMW), in LNCaP prostate cancer cells using the GSE149428 dataset (0, 3, 6, 9, 12, and 24 h). Expression values were first Z-score normalized, and the 1,000 most variably expressed genes were selected. To ensure coordinated temporal dynamics, we calculated Pearson correlation coefficients among these genes and retained those with r ≥ 0.5, resulting in 999 strongly co-expressed candidates. We then constructed a protein-protein interaction network for these genes and embedded it in two dimensions using the Kamada-Kawai force-directed algorithm. Finally, for each time point and treatment, we mapped the normalized expression values of the corresponding genes onto the fixed Kamada-Kawai layout as Gaussian density fields (σ = 0.03), generating a distinct Temporal GeneTerrain map for each time-condition combination.

Results: The application of Temporal GeneTerrain revealed intricate temporal shifts in gene expression, particularly unveiling delayed responses in pathways such as NGF-stimulated transcription and the unfolded protein response under combined drug treatments. Compared to traditional heatmap visualizations, Temporal GeneTerrain significantly improved both resolution and interpretability, effectively capturing gene expression patterns' multidimensional and transient nature. This enhancement provides a solid foundation for further research and analysis, assuring the scientific community of the method's reliability.

Discussion: Temporal GeneTerrain addresses the limitations of traditional visualization methods by offering an intuitive and detailed representation of gene expression dynamics. Compared to other approaches, such as heatmaps and static clustering, Temporal GeneTerrain uniquely captures the transient nature of gene expression patterns. This method significantly enhances the interpretability of complex biological datasets, thereby supporting informed decision-making in biological research and therapeutic development.

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