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The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway
miRNAs are non-coding RNA molecules typically 18–22 nucleotides long that can suppress the expression of their target genes. Several laboratories have attempted to identify miRNAs from the pig that are involved in Salmonella infection. These bioinformatics strategies using the newly available genomi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006312/ https://www.ncbi.nlm.nih.gov/pubmed/27474500 http://dx.doi.org/10.1042/BSR20160243 |
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author | Yao, Min Gao, Weihua Yang, Jun Liang, Xiongyan Luo, Jingbo Huang, Tinghua |
author_facet | Yao, Min Gao, Weihua Yang, Jun Liang, Xiongyan Luo, Jingbo Huang, Tinghua |
author_sort | Yao, Min |
collection | PubMed |
description | miRNAs are non-coding RNA molecules typically 18–22 nucleotides long that can suppress the expression of their target genes. Several laboratories have attempted to identify miRNAs from the pig that are involved in Salmonella infection. These bioinformatics strategies using the newly available genomic sequence are generally successful. Here, we report an in silico identification of miRNAs in pig focusing on the Salmonella infection pathway, and further investigated the differential expression of those miRNAs by quantitative real-time PCR during pre- and post-natal stage of Salmonella inoculation from the peripheral blood of commercially breed pigs. We identified 29 miRNAs that have predicted targets in the Salmonella infection pathway and nine of them were not yet described in pig. In addition, the expression of nine selected miRNAs was validated in the peripheral blood by northern blotting. Through expression analyses, differences were found between pre- and post-natal stages of Salmonella inoculation for miR-221, miR-125b and miR-27b—all of them were suppressed 2 days after Salmonella inoculation. The predicted targets of those three miRNAs were validated by luciferase reporter assays. We show that FOS is a direct target of miR-221, miR-125b can suppress MAPK14, and miR-27b can target IFNG. These findings will be helpful in understanding the function and processing of these miRNAs in Salmonella infection. The miRNA differentially expressed in the peripheral blood of commercial breed pigs suggest that it can be used as genetic markers for salmonella infection resistance in pigs. |
format | Online Article Text |
id | pubmed-5006312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50063122016-09-09 The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway Yao, Min Gao, Weihua Yang, Jun Liang, Xiongyan Luo, Jingbo Huang, Tinghua Biosci Rep Original Papers miRNAs are non-coding RNA molecules typically 18–22 nucleotides long that can suppress the expression of their target genes. Several laboratories have attempted to identify miRNAs from the pig that are involved in Salmonella infection. These bioinformatics strategies using the newly available genomic sequence are generally successful. Here, we report an in silico identification of miRNAs in pig focusing on the Salmonella infection pathway, and further investigated the differential expression of those miRNAs by quantitative real-time PCR during pre- and post-natal stage of Salmonella inoculation from the peripheral blood of commercially breed pigs. We identified 29 miRNAs that have predicted targets in the Salmonella infection pathway and nine of them were not yet described in pig. In addition, the expression of nine selected miRNAs was validated in the peripheral blood by northern blotting. Through expression analyses, differences were found between pre- and post-natal stages of Salmonella inoculation for miR-221, miR-125b and miR-27b—all of them were suppressed 2 days after Salmonella inoculation. The predicted targets of those three miRNAs were validated by luciferase reporter assays. We show that FOS is a direct target of miR-221, miR-125b can suppress MAPK14, and miR-27b can target IFNG. These findings will be helpful in understanding the function and processing of these miRNAs in Salmonella infection. The miRNA differentially expressed in the peripheral blood of commercial breed pigs suggest that it can be used as genetic markers for salmonella infection resistance in pigs. Portland Press Ltd. 2016-08-31 /pmc/articles/PMC5006312/ /pubmed/27474500 http://dx.doi.org/10.1042/BSR20160243 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution Licence 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Papers Yao, Min Gao, Weihua Yang, Jun Liang, Xiongyan Luo, Jingbo Huang, Tinghua The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway |
title | The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway |
title_full | The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway |
title_fullStr | The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway |
title_full_unstemmed | The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway |
title_short | The regulation roles of miR-125b, miR-221 and miR-27b in porcine Salmonella infection signalling pathway |
title_sort | regulation roles of mir-125b, mir-221 and mir-27b in porcine salmonella infection signalling pathway |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006312/ https://www.ncbi.nlm.nih.gov/pubmed/27474500 http://dx.doi.org/10.1042/BSR20160243 |
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