Central Laboratory, Translational Medicine Research Center, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing, 211100, Jiangsu, China.
Department of Gynecology and Obstetrics, The Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing, 211100, Jiangsu, China.
Arch Gynecol Obstet. 2020 Apr;301(4):963-971. doi: 10.1007/s00404-020-05495-5. Epub 2020 Mar 19.
Circular RNAs (circRNAs) are widely expressed noncoding RNAs which play important roles in various processes. The present study aimed to explore the effect of maternal PCOS on the expression of circRNAs in fetus and assessed the potential role of circRNA in human ovarian granulosa cell proliferation.
Total RNA was extracted from the fetal side of placental tissues from maternal PCOS (n = 3) and healthy puerpera (n = 3) for circRNA microarray. Real-time reverse transcriptase quantitative PCR (RT-qPCR) was used to validate the microarray data in fetal side of placental tissues from puerpera with (n = 18) and without (n = 30) PCOS. Gene Ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were applied to predict the functions and pathways of circ_0023942 host genes. The circRNA-miRNA-mRNA network was constructed through bioinformatics prediction. Circ_0023942 overexpression vector was transiently transfected into human ovarian granulosa cell lines KGN and COV434. Cell proliferation was detected by cell counting kit-8. The protein expression level was determined by western blot.
Compared with healthy puerpera, 14 circRNAs were significantly upregulated and 101 circRNAs were significantly downregulated in the fetal side of placenta from maternal PCOS according to the microarray data. Six differentially expressed circRNAs were selected for validation by RT-qPCR, and the expression patterns of circ_0023942, circ_0002151, circ_0001274, and circ_0008514 were consistent with the microarray data. Circ_0023942 was chosen for further investigation. GO and KEGG analysis predicted that circ_0023942 participated in the regulation of developmental process and the MAPK signaling pathway. Seven miRNAs were predicted to be the targets of circ_0023942. Overexpression of circ_0023942 inhibited human ovarian granulosa cell proliferation and suppressed the expression of CDK-4.
Maternal PCOS impairs circ_0023942 expression in fetus. Overexpression of circ_0023942 inhibits human ovarian granulosa cell proliferation possibly via regulating CDK-4.
环状 RNA(circRNA)是广泛表达的非编码 RNA,在各种过程中发挥重要作用。本研究旨在探讨母体 PCOS 对胎儿中 circRNA 表达的影响,并评估 circRNA 在人卵巢颗粒细胞增殖中的潜在作用。
从母体 PCOS(n=3)和健康产妇(n=3)的胎盘组织胎儿侧提取总 RNA,进行 circRNA 微阵列分析。实时逆转录定量 PCR(RT-qPCR)用于验证产妇胎盘组织胎儿侧 PCOS 患者(n=18)和无 PCOS 患者(n=30)的微阵列数据。通过基因本体论(GO)分析和京都基因与基因组百科全书(KEGG)分析预测 circ_0023942 宿主基因的功能和途径。通过生物信息学预测构建 circRNA-miRNA-mRNA 网络。瞬时转染 circ_0023942 过表达载体至人卵巢颗粒细胞系 KGN 和 COV434。通过细胞计数试剂盒-8 检测细胞增殖。通过 Western blot 测定蛋白表达水平。
根据微阵列数据,与健康产妇相比,母体 PCOS 胎盘组织胎儿侧有 14 个 circRNA 显著上调,101 个 circRNA 显著下调。通过 RT-qPCR 验证了 6 个差异表达的 circRNA,circ_0023942、circ_0002151、circ_0001274 和 circ_0008514 的表达模式与微阵列数据一致。选择 circ_0023942 进行进一步研究。GO 和 KEGG 分析预测 circ_0023942 参与了发育过程和 MAPK 信号通路的调节。预测到 7 个 miRNA 是 circ_0023942 的靶标。circ_0023942 的过表达抑制了人卵巢颗粒细胞的增殖,并抑制了 CDK-4 的表达。
母体 PCOS 损害胎儿中 circ_0023942 的表达。circ_0023942 的过表达可能通过调节 CDK-4 抑制人卵巢颗粒细胞的增殖。