Eudowood Division of Pediatric Respiratory Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Division of Pulmonary and Critical Care Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Sci Rep. 2020 May 4;10(1):7479. doi: 10.1038/s41598-020-64514-2.
People with ataxia-telangiectasia (A-T) display phenotypic variability with regard to progression of immunodeficiency, sino-pulmonary disease, and neurologic decline. To determine the association between differential gene expression, epigenetic state, and phenotypic variation among people with A-T, we performed transcriptional and genome-wide DNA methylation profiling in patients with mild and classic A-T progression as well as healthy controls. RNA and genomic DNA were isolated from peripheral blood mononuclear cells for transcriptional and DNA methylation profiling with RNA-sequencing and modified reduced representation bisulfite sequencing, respectively. We identified 555 genes that were differentially expressed among the control, mild A-T, and classic A-T groups. Genome-wide DNA methylation profiling revealed differential promoter methylation in cis with 146 of these differentially expressed genes. Functional enrichment analysis identified significant enrichment in immune, growth, and apoptotic pathways among the methylation-regulated genes. Regardless of clinical phenotype, all A-T participants exhibited downregulation of critical genes involved in B cell function (PAX5, CD79A, CD22, and FCRL1) and upregulation of several genes associated with senescence and malignancy, including SERPINE1. These findings indicate that gene expression differences may be associated with phenotypic variability and suggest that DNA methylation regulates expression of critical immune response genes in people with A-T.
共济失调毛细血管扩张症(A-T)患者的免疫缺陷、肺-鼻窦疾病和神经功能下降的进展存在表型变异性。为了确定 A-T 患者之间差异基因表达、表观遗传状态和表型变异之间的关联,我们对轻度和经典 A-T 进展以及健康对照者进行了转录组和全基因组 DNA 甲基化谱分析。从外周血单核细胞中分离 RNA 和基因组 DNA,分别进行 RNA 测序和改良的简化代表性双测序的转录组和 DNA 甲基化谱分析。我们在对照组、轻度 A-T 和经典 A-T 组之间鉴定出 555 个差异表达的基因。全基因组 DNA 甲基化谱分析显示,这些差异表达基因中有 146 个基因的顺式启动子甲基化存在差异。功能富集分析发现,在受甲基化调控的基因中,免疫、生长和凋亡途径显著富集。无论临床表型如何,所有 A-T 参与者均表现出与 B 细胞功能相关的关键基因(PAX5、CD79A、CD22 和 FCRL1)下调,以及与衰老和恶性相关的多个基因(包括 SERPINE1)上调。这些发现表明基因表达差异可能与表型变异性有关,并表明 DNA 甲基化调节 A-T 患者关键免疫反应基因的表达。