Hindmarch Charles C T, Potus François, Al-Qazazi Ruaa, Ott Benjamin P, Nichols William C, Rauh Michael J, Archer Stephen L
Department of Biomedical and Molecular Science (DBMS), Queen's University, Kingston, Ontario, Canada.
Department of Medicine, Queen's University, Kingston, Ontario, Canada.
Compr Physiol. 2025 Apr;15(2):e70011. doi: 10.1002/cph4.70011.
Epigenetic changes in gene expression due to DNA methylation regulate pulmonary vascular structure and function. Genetic or acquired alterations in DNA methylation/demethylation can promote the development of pulmonary arterial hypertension (PAH). Here, we performed epigenome-wide mapping of DNA methylation in whole blood from 10 healthy people and 19 age/sex-matched PAH patients from the PAH Biobank. Exome sequencing confirmed the absence of known mutations in PAH-associated gene variants identifying subjects with or without mutations of TET2, a putative PAH gene encoding the demethylating enzyme, TET2. DNA of patients with PAH and no TET2 mutation was hypermethylated compared to healthy controls. Patients with PAH and a TET2 mutation had greater DNA CpG methylation than mutation-free PAH patients. Unique Differentially Methylated Regions (DMR) were more common in patients with PAH with TET2 mutations (1164) than in PAH without mutations (262). We correlated methylome findings with a public PAH transcriptomic RNA dataset, prioritizing targets that are both hypermethylated in our cohort and downregulated at the RNA level. Relative to controls, functional analysis reveals enriched functions related to T cell differentiation in PAH patients with a TET2 mutation. We identified genes with downregulated expression that were hypermethylated in PAH patients (with or without a TET2 mutation). In both cases, a conserved T cell phenotype emerged. Pan-chromosomal hypermethylation in PAH is greatest in patients with TET2 mutations. Observed hypermethylation of genes involved in the pathogenesis of PAH, such as EIF2AK4, and transcription factors that regulate T cell development, such as TCF7, merit further study and may contribute to the inflammation in PAH.
由于DNA甲基化导致的基因表达表观遗传变化调节肺血管结构和功能。DNA甲基化/去甲基化的遗传或后天改变可促进肺动脉高压(PAH)的发展。在此,我们对来自PAH生物样本库的10名健康人和19名年龄/性别匹配的PAH患者的全血进行了全基因组DNA甲基化图谱分析。外显子组测序证实PAH相关基因变异中不存在已知突变,这些变异可识别有无推定的PAH基因TET2突变的受试者,TET2编码去甲基化酶。与健康对照相比,无TET2突变的PAH患者的DNA发生了高甲基化。有TET2突变的PAH患者比无突变的PAH患者具有更高的DNA CpG甲基化。独特的差异甲基化区域(DMR)在有TET2突变的PAH患者(1164个)中比无突变的PAH患者(262个)更常见。我们将甲基化组研究结果与公开的PAH转录组RNA数据集进行关联,优先考虑在我们的队列中高甲基化且在RNA水平下调的靶点。相对于对照,功能分析揭示了有TET2突变的PAH患者中与T细胞分化相关的功能富集。我们鉴定出在PAH患者(有或无TET2突变)中高甲基化且表达下调的基因。在这两种情况下,都出现了保守的T细胞表型。PAH中的全染色体高甲基化在有TET2突变的患者中最为明显。观察到参与PAH发病机制的基因如EIF2AK4以及调节T细胞发育的转录因子如TCF7的高甲基化,值得进一步研究,可能与PAH中的炎症有关。