Cardio Vascular Diseases and Diabetes Biology, Rajiv Gandhi Centre for Biotechnology, Poojappura, Thycaud, Thiruvananthapuram, Kerala, India, 695014.
Department of Biotechnology, Bhupat and Jyoti Mehta School of Biosciences, Indian Institute of Technology, Madras, Chennai, Tamil Nadu, 600036, India.
Clin Epigenetics. 2022 Oct 13;14(1):127. doi: 10.1186/s13148-022-01346-z.
Arteriovenous malformation (AVM) is a tangle of arteries and veins, rupture of which can result in catastrophic hemorrhage in vulnerable sites such as the brain. Cerebral AVM is associated with a high mortality rate in humans. The causative factor or the stimulus at the artery-venous junction and the molecular basis of the development and progression of cerebral AVM remain unknown. While it is known that aberrant hemodynamic forces in the artery-vein junction contribute to the development of AVMs, the mechanistic pathways are unclear. Given that various environmental stimuli modulate epigenetic modifications on the chromatin of cells, we speculated that misregulated DNA methylome could lead to cerebral AVM development. To identify the aberrant epigenetic signatures, we used AVM nidus tissues and analyzed the global DNA methylome using the Infinium DNA methylome array. We observed significant alterations of DNA methylation in the genes associated with the vascular developmental pathway. Further, we validated the DNA hypermethylation by DNA bisulfite sequencing analysis of selected genes from human cerebral AVM nidus. Taken together, we provide the first experimental evidence for aberrant epigenetic signatures on the genes of vascular development pathway, in human cerebral AVM nidus.
动静脉畸形(AVM)是动脉和静脉的缠绕,其破裂可导致大脑等脆弱部位灾难性出血。脑动静脉畸形与人类的高死亡率有关。在动静脉交界处导致 AVM 的致病因素或刺激因素以及脑 AVM 发展和进展的分子基础仍不清楚。虽然已知动脉静脉交界处异常的血流动力会促进 AVM 的发展,但具体的机制途径尚不清楚。鉴于各种环境刺激可以调节细胞染色质上的表观遗传修饰,我们推测异常的 DNA 甲基化组可能导致脑 AVM 的发展。为了鉴定异常的表观遗传特征,我们使用 AVM 核心组织,并使用 Infinium DNA 甲基化组芯片分析了全基因组 DNA 甲基化。我们观察到与血管发育途径相关的基因中的 DNA 甲基化发生了显著改变。此外,我们通过对人类脑 AVM 核心组织中的选定基因进行 DNA 亚硫酸氢盐测序分析,验证了 DNA 的高甲基化。总之,我们为人类脑 AVM 核心组织中血管发育途径的基因上存在异常的表观遗传特征提供了第一个实验证据。