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Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks
Female fertility is a highly regulated process involving the synchronized activities of multiple tissues. The underlying genomic regulation of the tissue synchronization is poorly understood. To understand this better we investigated the transcriptomes of the porcine ovary, endometrium, and oviduct...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882957/ https://www.ncbi.nlm.nih.gov/pubmed/29615657 http://dx.doi.org/10.1038/s41598-018-23655-1 |
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author | Kim, Jun-Mo Park, Jong-Eun Yoo, Inkyu Han, Jisoo Kim, Namshin Lim, Won-Jun Cho, Eun-Seok Choi, Bonghwan Choi, Sunho Kim, Tae-Hun te Pas, Marinus F. W. Ka, Hakhyun Lee, Kyung-Tai |
author_facet | Kim, Jun-Mo Park, Jong-Eun Yoo, Inkyu Han, Jisoo Kim, Namshin Lim, Won-Jun Cho, Eun-Seok Choi, Bonghwan Choi, Sunho Kim, Tae-Hun te Pas, Marinus F. W. Ka, Hakhyun Lee, Kyung-Tai |
author_sort | Kim, Jun-Mo |
collection | PubMed |
description | Female fertility is a highly regulated process involving the synchronized activities of multiple tissues. The underlying genomic regulation of the tissue synchronization is poorly understood. To understand this better we investigated the transcriptomes of the porcine ovary, endometrium, and oviduct at days 0, 3, 6, 9, 12, 15, or 18 of the oestrous cycle. We analysed the transcriptome profiles of the individual tissues and focus on the bridging genes shared by two or more tissues. The three tissue-networks were connected forming a triangular shape. We identified 65 bridging genes with a high level of connectivity to all other genes in the network. The expression levels showed negative correlations between the ovary and the other two tissues, and low correlations between endometrium and oviduct. The main functional annotations involved biosynthesis of steroid hormones, cell-to-cell adhesion, and cell apoptosis, suggesting that regulation of steroid hormone synthesis and tissue viability are major regulatory mechanisms. |
format | Online Article Text |
id | pubmed-5882957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58829572018-04-09 Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks Kim, Jun-Mo Park, Jong-Eun Yoo, Inkyu Han, Jisoo Kim, Namshin Lim, Won-Jun Cho, Eun-Seok Choi, Bonghwan Choi, Sunho Kim, Tae-Hun te Pas, Marinus F. W. Ka, Hakhyun Lee, Kyung-Tai Sci Rep Article Female fertility is a highly regulated process involving the synchronized activities of multiple tissues. The underlying genomic regulation of the tissue synchronization is poorly understood. To understand this better we investigated the transcriptomes of the porcine ovary, endometrium, and oviduct at days 0, 3, 6, 9, 12, 15, or 18 of the oestrous cycle. We analysed the transcriptome profiles of the individual tissues and focus on the bridging genes shared by two or more tissues. The three tissue-networks were connected forming a triangular shape. We identified 65 bridging genes with a high level of connectivity to all other genes in the network. The expression levels showed negative correlations between the ovary and the other two tissues, and low correlations between endometrium and oviduct. The main functional annotations involved biosynthesis of steroid hormones, cell-to-cell adhesion, and cell apoptosis, suggesting that regulation of steroid hormone synthesis and tissue viability are major regulatory mechanisms. Nature Publishing Group UK 2018-04-03 /pmc/articles/PMC5882957/ /pubmed/29615657 http://dx.doi.org/10.1038/s41598-018-23655-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Jun-Mo Park, Jong-Eun Yoo, Inkyu Han, Jisoo Kim, Namshin Lim, Won-Jun Cho, Eun-Seok Choi, Bonghwan Choi, Sunho Kim, Tae-Hun te Pas, Marinus F. W. Ka, Hakhyun Lee, Kyung-Tai Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks |
title | Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks |
title_full | Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks |
title_fullStr | Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks |
title_full_unstemmed | Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks |
title_short | Integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks |
title_sort | integrated transcriptomes throughout swine oestrous cycle reveal dynamic changes in reproductive tissues interacting networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882957/ https://www.ncbi.nlm.nih.gov/pubmed/29615657 http://dx.doi.org/10.1038/s41598-018-23655-1 |
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