Ham Seokjin, Oh Yeon-Mok, Roh Tae-Young
Department of Life Sciences, POSTECH, Pohang 37674, Korea.
Department of Pulmonary and Critical Care Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Genomics Inform. 2019 Mar;17(1):e2. doi: 10.5808/GI.2019.17.1.e2. Epub 2019 Mar 31.
Chronic obstructive pulmonary disease (COPD) is a type of progressive lung disease, featured by airflow obstruction. Recently, a comprehensive analysis of the transcriptome in lung tissue of COPD patients was performed, but the heterogeneity of the sample was not seriously considered in characterizing the mechanistic dysregulation of COPD. Here, we established a new transcriptome analysis pipeline using a deconvolution process to reduce the heterogeneity and clearly identified that these transcriptome data originated from the mild or moderate stage of COPD patients. Differentially expressed or co-expressed genes in the protein interaction subnetworks were linked with mitochondrial dysfunction and the immune response, as expected. Computational protein localization prediction revealed that 19 proteins showing changes in subcellular localization were mostly related to mitochondria, suggesting that mislocalization of mitochondria-targeting proteins plays an important role in COPD pathology. Our extensive evaluation of COPD transcriptome data could provide guidelines for analyzing heterogeneous gene expression profiles and classifying potential candidate genes that are responsible for the pathogenesis of COPD.
慢性阻塞性肺疾病(COPD)是一种以气流受限为特征的进行性肺部疾病。最近,对COPD患者肺组织中的转录组进行了全面分析,但在表征COPD的机制失调时,未充分考虑样本的异质性。在此,我们建立了一种新的转录组分析流程,通过去卷积过程减少异质性,并明确鉴定出这些转录组数据源自COPD患者的轻度或中度阶段。正如预期的那样,蛋白质相互作用子网中差异表达或共表达的基因与线粒体功能障碍和免疫反应相关。计算蛋白质定位预测显示,19种亚细胞定位发生变化的蛋白质大多与线粒体相关,这表明靶向线粒体的蛋白质的错误定位在COPD病理过程中起重要作用。我们对COPD转录组数据的广泛评估可为分析异质基因表达谱和分类导致COPD发病机制的潜在候选基因提供指导。