H19 Promoter DNA Methylation is Lower Among Early Abortion Patients Undergoing IVF Embryo Transfer

DNA甲基化 CpG站点 甲基化 生物 表观遗传学 亚硫酸氢盐测序 男科 基因组印记 分子生物学 DNMT1型 胚胎 绒毛 基因表达 胎盘 遗传学 基因 怀孕 胎儿 医学
作者
Lei Han,Xianghui Zhang,Xiaohan Wu,Huishu Xu,Bao‐Lin Zhang,Yiwei Pang,Pei‐Hui Ding,Caiying Zhang,Yanlin Wang,Jiajia An
出处
期刊:Clinical and Investigative Medicine 卷期号:46 (3): E13-18 被引量:1
标识
DOI:10.25011/cim.v46i3.41654
摘要

H19 is the first long noncoding RNA (lncRNA) found to be associated with gene imprinting. It is highly expressed in the embryonic stage and may have important regulatory effects on human embryonic development. We investigated the differences between the levels of H19 promoter DNA methylation in the chorionic villi of patients who experienced spontaneous abortion (SA) following in vitro fertilization embryo transfer (IVF-ET) and those of patients with a normal early pregnancy (NEP). We also analyzed the associated DNA methyltransferase (DNMT) activity.Chorionic villus tissue from patients with SA and NEP were collected. The DNA methylation levels of two CpG islands in the promoter region of the H19 gene in the two groups were detected by bisulfite sequencing, and the mRNA expression of DNMTs was analyzed by real-time polymerase chain reaction.The sample size of each group was 32, and there were no significant differences in baseline data, including age, parity, and body mass index, between the two groups. Among the 7 CpG islands measured, the methylation rates of 3 CpG islands (CpG 1, 6, and 7) were significantly lower in the SA group than in the NEP group (P < 0.01). The methylation levels of the other 4 CpG islands were not significantly different between the two groups. There were no differences in the expression of DNMT1 between the two groups (P > 0.05), but DNMT3a and DNMT3b RNA levels were significantly lower in SA group than in the NEP group (P < 0.01).The lower H19 promoter DNA methylation levels found in the chorionic villi of patients with SA patients following IVF-ET may be explained by decreased expression of DNMT3a and DNMT3b.
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