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MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection
MicroRNA (miRNA) is small non-coding RNA with approximate 22 nt in length. Recent studies indicate that miRNAs play significant roles in pathogen-host interactions. Brucella organisms are Gram-negative facultative intracellular bacteria that cause Brucellosis. Brucella strains infect macrophages and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3421232/ https://www.ncbi.nlm.nih.gov/pubmed/22904669 http://dx.doi.org/10.7150/ijbs.3836 |
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author | Zheng, Ke Chen, Dong-Sheng Wu, Yi-Quan Xu, Xian-Jin Zhang, Hui Chen, Chuang-Fu Chen, Huan-Chun Liu, Zheng-Fei |
author_facet | Zheng, Ke Chen, Dong-Sheng Wu, Yi-Quan Xu, Xian-Jin Zhang, Hui Chen, Chuang-Fu Chen, Huan-Chun Liu, Zheng-Fei |
author_sort | Zheng, Ke |
collection | PubMed |
description | MicroRNA (miRNA) is small non-coding RNA with approximate 22 nt in length. Recent studies indicate that miRNAs play significant roles in pathogen-host interactions. Brucella organisms are Gram-negative facultative intracellular bacteria that cause Brucellosis. Brucella strains infect macrophages and establish chronic infection by altering host life activities including apoptosis and autophagy. Here, we report a comprehensive analysis of miRNA expression profiles in mock- and Brucella-infected RAW264.7 cells using high-throughput sequencing approach. In total, 344 unique miRNAs were co-expressed in the two libraries, in which 57 miRNAs were differentially expressed. Eight differentially expressed miRNAs with high abundance were subjected to further analysis. The GO enrichment analysis suggests that the putative target genes of these differentially expressed miRNAs are involved in apoptosis, autophagy and immune response. In particular, a total of 25 target genes are involved in regulating apoptosis and autophagy, indicating that these miRNAs may play important regulatory roles in the Brucella-host interactions. Furthermore, the interactions of miR-1981 and its target genes, Bcl-2 and Bid, were validated by luciferase assay. The results show that miR-1981 mimic up-regulated the luciferase activity of psiCHECK-2 Bcl-2 3′ UTR, but the luciferase activity of psiCHECK-2 Bid 3′ UTR was not changed significantly. Taken together, these data provide valuable framework on Brucella induced miRNA expression in RAW264.7 cells, and suggest that Brucella may establish chronic infection by regulating miRNA expression profile. |
format | Online Article Text |
id | pubmed-3421232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-34212322012-08-17 MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection Zheng, Ke Chen, Dong-Sheng Wu, Yi-Quan Xu, Xian-Jin Zhang, Hui Chen, Chuang-Fu Chen, Huan-Chun Liu, Zheng-Fei Int J Biol Sci Research Paper MicroRNA (miRNA) is small non-coding RNA with approximate 22 nt in length. Recent studies indicate that miRNAs play significant roles in pathogen-host interactions. Brucella organisms are Gram-negative facultative intracellular bacteria that cause Brucellosis. Brucella strains infect macrophages and establish chronic infection by altering host life activities including apoptosis and autophagy. Here, we report a comprehensive analysis of miRNA expression profiles in mock- and Brucella-infected RAW264.7 cells using high-throughput sequencing approach. In total, 344 unique miRNAs were co-expressed in the two libraries, in which 57 miRNAs were differentially expressed. Eight differentially expressed miRNAs with high abundance were subjected to further analysis. The GO enrichment analysis suggests that the putative target genes of these differentially expressed miRNAs are involved in apoptosis, autophagy and immune response. In particular, a total of 25 target genes are involved in regulating apoptosis and autophagy, indicating that these miRNAs may play important regulatory roles in the Brucella-host interactions. Furthermore, the interactions of miR-1981 and its target genes, Bcl-2 and Bid, were validated by luciferase assay. The results show that miR-1981 mimic up-regulated the luciferase activity of psiCHECK-2 Bcl-2 3′ UTR, but the luciferase activity of psiCHECK-2 Bid 3′ UTR was not changed significantly. Taken together, these data provide valuable framework on Brucella induced miRNA expression in RAW264.7 cells, and suggest that Brucella may establish chronic infection by regulating miRNA expression profile. Ivyspring International Publisher 2012-08-03 /pmc/articles/PMC3421232/ /pubmed/22904669 http://dx.doi.org/10.7150/ijbs.3836 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. |
spellingShingle | Research Paper Zheng, Ke Chen, Dong-Sheng Wu, Yi-Quan Xu, Xian-Jin Zhang, Hui Chen, Chuang-Fu Chen, Huan-Chun Liu, Zheng-Fei MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection |
title | MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection |
title_full | MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection |
title_fullStr | MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection |
title_full_unstemmed | MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection |
title_short | MicroRNA Expression Profile in RAW264.7 cells in Response to Brucella melitensis Infection |
title_sort | microrna expression profile in raw264.7 cells in response to brucella melitensis infection |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3421232/ https://www.ncbi.nlm.nih.gov/pubmed/22904669 http://dx.doi.org/10.7150/ijbs.3836 |
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