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The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation

BACKGROUND: Delayed implantation is a developmental arrest at the blastocyst stage and a good model for embryo implantation. MicroRNAs (miRNAs) have been shown to be involved in mouse embryo implantation through regulating uterine gene expression. This study was to have an integrative analysis on gl...

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Autores principales: Su, Ren-Wei, Lei, Wei, Liu, Ji-Long, Zhang, Zhi-Rong, Jia, Bo, Feng, Xu-Hui, Ren, Gang, Hu, Shi-Jun, Yang, Zeng-Ming
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993968/
https://www.ncbi.nlm.nih.gov/pubmed/21124741
http://dx.doi.org/10.1371/journal.pone.0015513
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author Su, Ren-Wei
Lei, Wei
Liu, Ji-Long
Zhang, Zhi-Rong
Jia, Bo
Feng, Xu-Hui
Ren, Gang
Hu, Shi-Jun
Yang, Zeng-Ming
author_facet Su, Ren-Wei
Lei, Wei
Liu, Ji-Long
Zhang, Zhi-Rong
Jia, Bo
Feng, Xu-Hui
Ren, Gang
Hu, Shi-Jun
Yang, Zeng-Ming
author_sort Su, Ren-Wei
collection PubMed
description BACKGROUND: Delayed implantation is a developmental arrest at the blastocyst stage and a good model for embryo implantation. MicroRNAs (miRNAs) have been shown to be involved in mouse embryo implantation through regulating uterine gene expression. This study was to have an integrative analysis on global miRNA and mRNA expression in mouse uterus under delayed implantation and activation through Illumina sequencing. METHODOLOGY/PRINCIPAL FINDINGS: By deep sequencing and analysis, we found that there are 20 miRNAs up-regulated and 42 miRNAs down-regulated at least 1.2 folds, and 268 genes up-regulated and 295 genes down-regulated at least 2 folds under activation compared to delayed implantation, respectively. Many different forms of editing in mature miRNAs are detected. The percentage of editing at positions 4 and 5 of mature miRNAs is significantly higher under delayed implantation than under activation. Although the number of miR-21 reference sequence under activation is slightly lower than that under delayed implantation, the total level of miR-21 under activation is higher than that under delayed implantation. Six novel miRNAs are predicted and confirmed. The target genes of significantly up-regulated miRNAs under activation are significantly enriched. CONCLUSIONS: miRNA and mRNA expression patterns are closely related. The target genes of up-regulated miRNAs are significantly enriched. A high level of editing at positions 4 and 5 of mature miRNAs is detected under delayed implantation than under activation. Our data should be valuable for future study on delayed implantation.
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spelling pubmed-29939682010-12-01 The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation Su, Ren-Wei Lei, Wei Liu, Ji-Long Zhang, Zhi-Rong Jia, Bo Feng, Xu-Hui Ren, Gang Hu, Shi-Jun Yang, Zeng-Ming PLoS One Research Article BACKGROUND: Delayed implantation is a developmental arrest at the blastocyst stage and a good model for embryo implantation. MicroRNAs (miRNAs) have been shown to be involved in mouse embryo implantation through regulating uterine gene expression. This study was to have an integrative analysis on global miRNA and mRNA expression in mouse uterus under delayed implantation and activation through Illumina sequencing. METHODOLOGY/PRINCIPAL FINDINGS: By deep sequencing and analysis, we found that there are 20 miRNAs up-regulated and 42 miRNAs down-regulated at least 1.2 folds, and 268 genes up-regulated and 295 genes down-regulated at least 2 folds under activation compared to delayed implantation, respectively. Many different forms of editing in mature miRNAs are detected. The percentage of editing at positions 4 and 5 of mature miRNAs is significantly higher under delayed implantation than under activation. Although the number of miR-21 reference sequence under activation is slightly lower than that under delayed implantation, the total level of miR-21 under activation is higher than that under delayed implantation. Six novel miRNAs are predicted and confirmed. The target genes of significantly up-regulated miRNAs under activation are significantly enriched. CONCLUSIONS: miRNA and mRNA expression patterns are closely related. The target genes of up-regulated miRNAs are significantly enriched. A high level of editing at positions 4 and 5 of mature miRNAs is detected under delayed implantation than under activation. Our data should be valuable for future study on delayed implantation. Public Library of Science 2010-11-29 /pmc/articles/PMC2993968/ /pubmed/21124741 http://dx.doi.org/10.1371/journal.pone.0015513 Text en Su et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Su, Ren-Wei
Lei, Wei
Liu, Ji-Long
Zhang, Zhi-Rong
Jia, Bo
Feng, Xu-Hui
Ren, Gang
Hu, Shi-Jun
Yang, Zeng-Ming
The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation
title The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation
title_full The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation
title_fullStr The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation
title_full_unstemmed The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation
title_short The Integrative Analysis of microRNA and mRNA Expression in Mouse Uterus under Delayed Implantation and Activation
title_sort integrative analysis of microrna and mrna expression in mouse uterus under delayed implantation and activation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993968/
https://www.ncbi.nlm.nih.gov/pubmed/21124741
http://dx.doi.org/10.1371/journal.pone.0015513
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