Identification of miR-192 target genes in porcine endometrial epithelial cells based on miRNA pull-down
- PMID: 36914869
- DOI: 10.1007/s11033-023-08349-w
Identification of miR-192 target genes in porcine endometrial epithelial cells based on miRNA pull-down
Abstract
Introduction: 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.
Methods: 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.
Results: 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.
Conclusion: 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.
Keywords: CSK; Porcine endometrial epithelial cells; Target gene; YY1; miR-192; miRNA pull-down.
© 2023. The Author(s), under exclusive licence to Springer Nature B.V.
References
-
- Avila-Bonilla RG, Salas-Benito JS (2022) Interactions of host miRNAs in the flavivirus 3′ UTR genome: from bioinformatics predictions to practical approaches. Front Cell Infect Microbiol 12:976843. https://doi.org/10.3389/fcimb.2022.976843 - DOI - PubMed - PMC
-
- Lewis BP, Burge CB, Bartel DP (2005) Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell 120(1):15–20. https://doi.org/10.1016/j.cell.2004.12.035 - DOI - PubMed
-
- Lal A, Thomas MP, Altschuler G, Navarro F, O’Day E, Li XL, Concepcion C, Han YC, Thiery J, Rajani DK, Deutsch A, Hofmann O, Ventura A, Hide W, Lieberman J (2011) Capture of microRNA-bound mRNAs identifies the tumor suppressor miR-34a as a regulator of growth factor signaling. PLoS Genet 7(11):e1002363. https://doi.org/10.1371/journal.pgen.1002363 - DOI - PubMed - PMC
-
- Ørom UA, Nielsen FC, Lund AH (2008) MicroRNA-10a binds the 5′ UTR of ribosomal protein mRNAs and enhances their translation. Mol Cell 30(4):460–471. https://doi.org/10.1016/j.molcel.2008.05.001 - DOI - PubMed
-
- Schnall-Levin M, Rissland OS, Johnston WK, Perrimon N, Bartel DP, Berger B (2011) Unusually effective microRNA targeting within repeat-rich coding regions of mammalian mRNAs. Genome Res 21(9):1395–1403. https://doi.org/10.1101/gr.121210.111 - DOI - PubMed - PMC
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