Rondel Filipp Martin, Farooq Hafsa, Hosseini Roya, Juyal Akshay, Knyazev Sergey, Mangul Serghei, Rogovskyy Artem S, Zelikovsky Alexander
Department of Computer Science, Georgia State University, Atlanta, Georgia, USA.
Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, California, USA.
J Comput Biol. 2025 Feb;32(2):188-197. doi: 10.1089/cmb.2024.0564. Epub 2024 Jun 27.
Evaluating changes in metabolic pathway activity is essential for studying disease mechanisms and developing new treatments, with significant benefits extending to human health. Here, we propose EMPathways2, a maximum likelihood pipeline that is based on the expectation-maximization algorithm, which is capable of evaluating enzyme expression and metabolic pathway activity level. We first estimate enzyme expression from RNA-seq data that is used for simultaneous estimation of pathway activity levels using enzyme participation levels in each pathway. We implement the novel pipeline to RNA-seq data from several groups of mice, which provides a deeper look at the biochemical changes occurring as a result of bacterial infection, disease, and immune response. Our results show that estimated enzyme expression, pathway activity levels, and enzyme participation levels in each pathway are robust and stable across all samples. Estimated activity levels of a significant number of metabolic pathways strongly correlate with the infected and uninfected status of the respective rodent types.
评估代谢途径活性的变化对于研究疾病机制和开发新疗法至关重要,对人类健康具有重大益处。在此,我们提出了EMPathways2,这是一种基于期望最大化算法的最大似然流程,能够评估酶表达和代谢途径活性水平。我们首先从RNA测序数据中估计酶表达,该数据用于利用每个途径中的酶参与水平同时估计途径活性水平。我们将这个新流程应用于几组小鼠的RNA测序数据,这能更深入地了解细菌感染、疾病和免疫反应导致的生化变化。我们的结果表明,每个途径中估计的酶表达、途径活性水平和酶参与水平在所有样本中都是稳健且稳定的。大量代谢途径的估计活性水平与相应啮齿动物类型的感染和未感染状态密切相关。