Department of Chemistry and Biotechnology, Tallinn University of Technology, Tallinn, Estonia.
Competence Centre on Health Technologies, Tartu, Estonia.
Sci Rep. 2020 Feb 10;10(1):2300. doi: 10.1038/s41598-020-59186-x.
MicroRNAs (miRNAs) are known post-transcriptional regulators of various biological processes including ovarian follicle development. We have previously identified miRNAs from human pre-ovulatory ovarian granulosa cells that are expressed from the intronic regions of two key genes in normal follicular development: FSH receptor (FSHR) and CYP19A1, the latter encoding the aromatase enzyme. The present study aims to identify the target genes regulated by these miRNAs: hsa-miR-548ba and hsa-miR-7973, respectively. The miRNAs of interest were transfected into KGN cell line and the gene expression changes were analyzed by Affymetrix microarray. Potential miRNA-regulated genes were further filtered by bioinformatic target prediction algorithms and validated for direct miRNA:mRNA binding by luciferase reporter assay. LIFR, PTEN, NEO1 and SP110 were confirmed as targets for hsa-miR-548ba. Hsa-miR-7973 target genes ADAM19, PXDN and FMNL3 also passed all verification steps. Additionally, the expression pattern of the miRNAs was studied in human primary cumulus granulosa cell culture in relation to the expression of their host genes and FSH stimulation. Based on our findings we propose the involvement of hsa-miR-548ba in the regulation of follicle growth and activation via LIFR and PTEN. Hsa-miR-7973 may be implicated in the modulation of extracellular matrix and cell-cell interactions by regulating the expression of its identified targets.
微小 RNA(miRNA)是各种生物过程的转录后调控因子,包括卵巢卵泡发育。我们之前已经从人类促排卵卵巢颗粒细胞中鉴定出 miRNA,这些 miRNA 来自正常卵泡发育的两个关键基因的内含子区域:促卵泡激素受体(FSHR)和 CYP19A1,后者编码芳香酶酶。本研究旨在鉴定这些 miRNA 调控的靶基因:hsa-miR-548ba 和 hsa-miR-7973。感兴趣的 miRNA 转染到 KGN 细胞系中,通过 Affymetrix 微阵列分析基因表达变化。通过生物信息学靶标预测算法进一步筛选潜在的 miRNA 调控基因,并通过荧光素酶报告基因测定验证直接 miRNA:mRNA 结合。LIFR、PTEN、NEO1 和 SP110 被确认为 hsa-miR-548ba 的靶标。hsa-miR-7973 的靶基因 ADAM19、PXDN 和 FMNL3 也通过了所有验证步骤。此外,还研究了 miRNA 在人原代卵丘颗粒细胞培养中的表达模式与宿主基因和 FSH 刺激的关系。基于我们的发现,我们提出 hsa-miR-548ba 通过调节 LIFR 和 PTEN 参与卵泡生长和激活的调控。hsa-miR-7973 可能通过调节其鉴定靶标的表达,参与细胞外基质和细胞-细胞相互作用的调节。