Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, 6997801, Israel.
Division of Medical Genetics, Department of Medicine, Department of Genome Sciences, Institute for Stem Cell and Regenerative Medicine, University of Washington School of Medicine, Seattle, WA, 98195, USA.
Sci Rep. 2018 Nov 26;8(1):17348. doi: 10.1038/s41598-018-35587-x.
The inner ear is a complex structure responsible for hearing and balance, and organ pathology is associated with deafness and balance disorders. To evaluate the role of epigenomic dynamics, we performed whole genome bisulfite sequencing at key time points during the development and maturation of the mouse inner ear sensory epithelium (SE). Our single-nucleotide resolution maps revealed variations in both general characteristics and dynamics of DNA methylation over time. This allowed us to predict the location of non-coding regulatory regions and to identify several novel candidate regulatory factors, such as Bach2, that connect stage-specific regulatory elements to molecular features that drive the development and maturation of the SE. Constructing in silico regulatory networks around sites of differential methylation enabled us to link key inner ear regulators, such as Atoh1 and Stat3, to pathways responsible for cell lineage determination and maturation, such as the Notch pathway. We also discovered that a putative enhancer, defined as a low methylated region (LMR), can upregulate the GJB6 gene and a neighboring non-coding RNA. The study of inner ear SE methylomes revealed novel regulatory regions in the hearing organ, which may improve diagnostic capabilities, and has the potential to guide the development of therapeutics for hearing loss by providing multiple intervention points for manipulation of the auditory system.
内耳是一个负责听觉和平衡的复杂结构,器官病理学与耳聋和平衡障碍有关。为了评估表观基因组动力学的作用,我们在小鼠内耳感觉上皮(SE)发育和成熟的关键时间点进行了全基因组亚硫酸氢盐测序。我们的单核苷酸分辨率图谱揭示了 DNA 甲基化随时间的一般特征和动态变化。这使我们能够预测非编码调控区域的位置,并鉴定出几个新的候选调控因子,如 Bach2,将特定阶段的调控元件与驱动 SE 发育和成熟的分子特征联系起来。围绕差异甲基化位点构建的计算机模拟调控网络使我们能够将关键的内耳调控因子,如 Atoh1 和 Stat3,与负责细胞谱系决定和成熟的途径(如 Notch 途径)联系起来。我们还发现,一个假定的增强子,定义为低甲基化区域(LMR),可以上调 GJB6 基因和一个相邻的非编码 RNA。对内耳 SE 甲基组的研究揭示了听力器官中的新调控区域,这可能提高诊断能力,并有可能通过为听觉系统的操作提供多个干预点来指导听力损失的治疗发展。