Jiang Li-Le, Xie Juan-Ke, Cui Jin-Quan, Wei Duo, Yin Bao-Li, Zhang Ya-Nan, Chen Yuan-Hui, Han Xiao, Wang Qian, Zhang Cui-Lian
aSecond Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan Province bZhengzhou University, Zhengzhou, Henan Province cReproductive Medical Center, People's Hospital of Henan Province, Zhengzhou, Henan Province, P.R. China.
Medicine (Baltimore). 2017 Jan;96(2):e5768. doi: 10.1097/MD.0000000000005768.
DNA methylation modification has been proved to influence the phenotype of polycystic ovary syndrome (PCOS). Genome-wide association studies (GWAS) demonstrate that yes-associated protein (YAP1) genetic sites are associated with PCOS. The study aims to detect the methylation status of YAP1 promoter in ovary granulosa cells (GCs) of PCOS patients and explore novel therapeutic targets for PCOS.
Randomized controlled trial was applied and a total of 72 women were included in the study, including 36 cases of PCOS patients and 36 cases of health controls. Ovary GCs were extracted from in vitro fertilization embryo transfer. Methylation status of YAP1 promoter was detected by bisulfite sequencing PCR (BSP). Protein and mRNA expression of YAP1 were measured by western blotting and real-time quantitate PCR.
Overall methylation level of YAP1 promoter region from PCOS group was significantly lower than that from control group. CpG sites analysis revealed that 12 sites (-443, -431, -403, -371, -331, -120, -49, -5, +1, +9, +15, +22) were significantly hypomethylated in women with PCOS (P < 0.05). A significant upregulation of YAP1 mRNA and protein expression levels was observed. Testosterone concentration could alleviate the methylation status and demonstrate obvious dose-dependent relation.
Our research achievements manifest that hypomethylation of YAP1 promoter promotes the YAP1 expression, which plays a key role in the pathogenesis and accelerate PCOS.
DNA甲基化修饰已被证明会影响多囊卵巢综合征(PCOS)的表型。全基因组关联研究(GWAS)表明,Yes相关蛋白(YAP1)基因位点与PCOS相关。本研究旨在检测PCOS患者卵巢颗粒细胞(GCs)中YAP1启动子的甲基化状态,并探索PCOS的新治疗靶点。
采用随机对照试验,共纳入72名女性,包括36例PCOS患者和36例健康对照。从体外受精胚胎移植中提取卵巢GCs。通过亚硫酸氢盐测序PCR(BSP)检测YAP1启动子的甲基化状态。通过蛋白质印迹法和实时定量PCR检测YAP1的蛋白质和mRNA表达。
PCOS组YAP1启动子区域的总体甲基化水平显著低于对照组。CpG位点分析显示,PCOS女性中有12个位点(-443、-431、-403、-371、-331、-120、-49、-5、+1、+9、+15、+22)显著低甲基化(P<0.05)。观察到YAP1 mRNA和蛋白质表达水平显著上调。睾酮浓度可减轻甲基化状态,并呈现明显的剂量依赖性关系。
我们的研究成果表明,YAP1启动子低甲基化促进YAP1表达,这在PCOS的发病机制中起关键作用并加速PCOS进程。