College of Animal Science and Technology, Shihezi University, 221 North Fourth Road, Shihezi, 832000, China.
Gembloux Agro-Bio Tech (ULiège-GxABT), University of Liège, Gembloux, Belgium.
Mol Biol Rep. 2023 May;50(5):4273-4284. doi: 10.1007/s11033-023-08349-w. Epub 2023 Mar 14.
MicroRNAs (miRNAs)-a class of small endogenous non-coding RNAs-are widely involved in post-transcriptional gene regulation of numerous physiological processes. High-throughput sequencing revealed that the miR-192 expression level appeared to be significantly higher in the blood exosomes of sows at early gestation than that in non-pregnant sows. Furthermore, miR-192 was hypothesized to have a regulatory role in embryo implantation; however, the target genes involved in exerting the regulatory function of miR-192 required further elucidation.
In the present study, potential target genes of miR-192 in porcine endometrial epithelial cells (PEECs) were identified through biotin-labeled miRNA pull-down; functional and pathway enrichment analysis was performed via gene ontology analysis and Kyoto Encyclopedia of Genes and Genomes pathway enrichment. Bioinformatic analyses were concurrently used to predict the potential target genes associated with sow embryo implantation. In addition, double luciferase reporter vectors, reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR), and Western blot were performed to verify the targeting and regulatory roles of the abovementioned target genes.
A total of 1688 differentially expressed mRNAs were identified via miRNA pull-down. Through RT-qPCR, the accuracy of the sequencing data was verified. In the bioinformatics analysis, potential target genes of miR-192 appeared to form a dense inter-regulatory network and regulated multiple signaling pathways, such as metabolic pathways and the PI3K-Akt, MAPKs, and mTOR signaling pathways, that are relevant to the mammalian embryo implantation process. In addition, CSK (C-terminal Src kinase) and YY1 (Yin-Yang-1) were predicted to be potential candidates, and we validated that miR-192 directly targets and suppresses the expression of the CSK and YY1 genes.
We screened 1688 potential target genes of miR-192 were screened, and CSK and YY1 were identified as miR-192 target genes. The outcomes of the present study provide novel insights into the regulatory mechanism of porcine embryo implantation and the identification of miRNA target genes.
微小 RNA(miRNAs)是一类小的内源性非编码 RNA,广泛参与众多生理过程的转录后基因调控。高通量测序显示,妊娠早期母猪血液外泌体中的 miR-192 表达水平明显高于非妊娠母猪。此外,miR-192 被假设在胚胎着床中具有调节作用,但发挥 miR-192 调节功能的靶基因仍需要进一步阐明。
本研究通过生物素标记 miRNA 下拉法鉴定猪子宫内膜上皮细胞(PEEC)中 miR-192 的潜在靶基因,通过基因本体分析和京都基因与基因组百科全书通路富集进行功能和通路富集分析。同时进行生物信息学分析,预测与母猪胚胎着床相关的潜在靶基因。此外,通过双荧光素酶报告载体、逆转录定量聚合酶链反应(RT-qPCR)和 Western blot 验证上述靶基因的靶向和调节作用。
通过 miRNA 下拉共鉴定出 1688 个差异表达的 mRNA。通过 RT-qPCR 验证了测序数据的准确性。在生物信息学分析中,miR-192 的潜在靶基因似乎形成了一个密集的相互调节网络,并调节了多个信号通路,如代谢通路以及 PI3K-Akt、MAPKs 和 mTOR 信号通路,这些通路与哺乳动物胚胎着床过程相关。此外,CSK(C 端Src 激酶)和 YY1(阴阳 1)被预测为潜在的候选基因,我们验证了 miR-192 可直接靶向并抑制 CSK 和 YY1 基因的表达。
我们筛选出了 1688 个 miR-192 的潜在靶基因,鉴定出 CSK 和 YY1 是 miR-192 的靶基因。本研究的结果为猪胚胎着床的调控机制和 miRNA 靶基因的鉴定提供了新的见解。