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miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development
BACKGROUND: Increasing evidence has shown that circular RNAs (circRNAs) are involved in neurodegenerative disorders, but their roles in neurological toxoplasmosis are yet to know. This study examined miRNA and circRNA expressions in mouse brain following oral infection with T. gondii Pru strain. RES...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958735/ https://www.ncbi.nlm.nih.gov/pubmed/31937240 http://dx.doi.org/10.1186/s12864-020-6464-9 |
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author | Zhou, Chun-Xue Ai, Kang Huang, Cui-Qin Guo, Jing-Jing Cong, Hua He, Shen-Yi Zhu, Xing-Quan |
author_facet | Zhou, Chun-Xue Ai, Kang Huang, Cui-Qin Guo, Jing-Jing Cong, Hua He, Shen-Yi Zhu, Xing-Quan |
author_sort | Zhou, Chun-Xue |
collection | PubMed |
description | BACKGROUND: Increasing evidence has shown that circular RNAs (circRNAs) are involved in neurodegenerative disorders, but their roles in neurological toxoplasmosis are yet to know. This study examined miRNA and circRNA expressions in mouse brain following oral infection with T. gondii Pru strain. RESULTS: Total RNA extracted from acutely infected (11 days post infection (DPI)), chronically infected (35 DPI) and uninfected mouse brain samples were subjected to genome-wide small RNA sequencing. In the acutely infected mice, 9 circRNAs and 20 miRNAs were upregulated, whereas 67 circRNAs and 28 miRNAs were downregulated. In the chronically infected mice, 2 circRNAs and 42 miRNAs were upregulated, whereas 1 circRNA and 29 miRNAs were downregulated. Gene ontology analysis predicted that the host genes that produced the dysregulated circRNAs in the acutely infected brain were primarily involved in response to stimulus and ion binding activities. Furthermore, predictive interaction networks of circRNA-miRNA and miRNA-mRNA were constructed based on genome-wide transcriptome sequencing and computational analyses, which might suggest the putative functions of miRNAs and circRNAs as a large class of post-transcriptional regulators. CONCLUSIONS: These findings will shed light on circRNA-miRNA interactions during the pathogenesis of toxoplasmosis, and they will lay solid foundation for studying the potential regulation roles of miRNAs and circRNAs in T. gondii induced pathogenesis. |
format | Online Article Text |
id | pubmed-6958735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69587352020-01-17 miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development Zhou, Chun-Xue Ai, Kang Huang, Cui-Qin Guo, Jing-Jing Cong, Hua He, Shen-Yi Zhu, Xing-Quan BMC Genomics Research Article BACKGROUND: Increasing evidence has shown that circular RNAs (circRNAs) are involved in neurodegenerative disorders, but their roles in neurological toxoplasmosis are yet to know. This study examined miRNA and circRNA expressions in mouse brain following oral infection with T. gondii Pru strain. RESULTS: Total RNA extracted from acutely infected (11 days post infection (DPI)), chronically infected (35 DPI) and uninfected mouse brain samples were subjected to genome-wide small RNA sequencing. In the acutely infected mice, 9 circRNAs and 20 miRNAs were upregulated, whereas 67 circRNAs and 28 miRNAs were downregulated. In the chronically infected mice, 2 circRNAs and 42 miRNAs were upregulated, whereas 1 circRNA and 29 miRNAs were downregulated. Gene ontology analysis predicted that the host genes that produced the dysregulated circRNAs in the acutely infected brain were primarily involved in response to stimulus and ion binding activities. Furthermore, predictive interaction networks of circRNA-miRNA and miRNA-mRNA were constructed based on genome-wide transcriptome sequencing and computational analyses, which might suggest the putative functions of miRNAs and circRNAs as a large class of post-transcriptional regulators. CONCLUSIONS: These findings will shed light on circRNA-miRNA interactions during the pathogenesis of toxoplasmosis, and they will lay solid foundation for studying the potential regulation roles of miRNAs and circRNAs in T. gondii induced pathogenesis. BioMed Central 2020-01-14 /pmc/articles/PMC6958735/ /pubmed/31937240 http://dx.doi.org/10.1186/s12864-020-6464-9 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Zhou, Chun-Xue Ai, Kang Huang, Cui-Qin Guo, Jing-Jing Cong, Hua He, Shen-Yi Zhu, Xing-Quan miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development |
title | miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development |
title_full | miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development |
title_fullStr | miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development |
title_full_unstemmed | miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development |
title_short | miRNA and circRNA expression patterns in mouse brain during toxoplasmosis development |
title_sort | mirna and circrna expression patterns in mouse brain during toxoplasmosis development |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6958735/ https://www.ncbi.nlm.nih.gov/pubmed/31937240 http://dx.doi.org/10.1186/s12864-020-6464-9 |
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