Expressions of miR-155 and miR-181 and predictions of their structures and targets in pigs ( Sus scrofa )

• Published in: Veterinary World 2020-08, Vol.13 (8), p.1667-1673
• Main Authors: Ninsuwon, Jirapat, Waiyamitra, Pitchaporn, Roongsitthichai, Atthaporn, Surachetpong, Win
• Format: Article
• Language: English
• Subjects: Animal diseases; B cells; CD4 antigen; Cell differentiation; Complementarity; Foxp1 protein; Gene expression; Genes; Immune response; immune system; Internet; Lymph nodes; Lymphocytes B; Lymphocytes T; Medical research; MicroRNA; mir-155; mir-181; miRNA; Muscles; Peripheral blood; Polymerase chain reaction; porcine; Post-transcription; Signal transduction; Slaughter; Spleen; Swine; T cell receptors; T cells; Transcription (Genetics)
• ISSN: 0972-8988; 2231-0916
• DOI: 10.14202/vetworld.2020.1667-1673

MicroRNAs (miRNAs) are responsible for gene expression control at the post-transcription level in many species. Several miRNAs are required in the regulation of immune responses, such as B-cell differentiation, T-cell receptor signaling pathway, CD4 T cell selection, and so on. Studies on miRNAs have been extensively conducted in humans and mice; however, reports relevant to miRNAs, especially miR-155 and miR-181, in pigs are limited. Consequently, the present study aimed to investigate the structures, target genes, and expressions of miR-155 and miR-181 in various porcine cells and tissues. Five healthy male pigs from a porcine reproductive and respiratory syndrome virus-negative farm were studied. Before slaughter, blood samples were collected for peripheral blood mononuclear cell isolation. After slaughter, samples of spleen, lymph nodes, and forelimb muscles were collected. Both miR-155 and miR-181 were investigated for their structures with RNAfold web server, for their target genes from three online web servers, and for their expressions using polymerase chain reaction (PCR). The structures of miR-155 and miR-181 contained hairpins with free energies of -35.27 and -35.29 kcal/mole, respectively. Target gene prediction revealed that miR-155 had perfect complementarity with and , while miR-181 had perfect complementarity with , and . PCR showed that both miRNAs were detectable from all investigated cells and tissues. Moreover, the highest expression of both miRNAs was found from the lymph node of the pigs. Both miR-155 and miR-181 might be involved with the regulation of porcine immune functions as both miRNAs were detected in several cells and tissues of the pigs. In addition, they had very high complementarities with the seed regions of several immune-related genes.