MicroRNA Expression Profile in Bovine Granulosa Cells of Preovulatory Dominant and Subordinate Follicles during the Late Follicular Phase of the Estrous Cycle
In bovine, ovarian follicles grow in a wave-like fashion with commonly 2 or 3 follicular waves emerging per estrous cycle. The dominant follicle of the follicular wave which coincides with the LH-surge becomes ovulatory, leaving the subordinate follicles to undergo atresia. These physiological proce...
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creator | Gebremedhn, Samuel Salilew-Wondim, Dessie Ahmad, Ijaz Sahadevan, Sudeep Hossain, Md Munir Hoelker, Michael Rings, Franca Neuhoff, Christiane Tholen, Ernst Looft, Christian Schellander, Karl Tesfaye, Dawit |
description | In bovine, ovarian follicles grow in a wave-like fashion with commonly 2 or 3 follicular waves emerging per estrous cycle. The dominant follicle of the follicular wave which coincides with the LH-surge becomes ovulatory, leaving the subordinate follicles to undergo atresia. These physiological processes are controlled by timely and spatially expressed genes and gene products, which in turn are regulated by post-transcriptional regulators. MicroRNAs, a class of short non-coding RNA molecules, are one of the important posttranscriptional regulators of genes associated with various cellular processes. Here we investigated the expression pattern of miRNAs in granulosa cells of bovine preovulatory dominant and subordinate follicles during the late follicular phase of bovine estrous cycle using Illumina miRNA deep sequencing. In addition to 11 putative novel miRNAs, a total of 315 and 323 known miRNAs were detected in preovulatory dominant and subordinate follicles, respectively. Moreover, in comparison with the subordinate follicles, a total of 64 miRNAs were found to be differentially expressed in preovulatory dominant follicles, of which 34 miRNAs including the miR-132 and miR-183 clusters were significantly enriched, and 30 miRNAs including the miR-17-92 cluster, bta-miR-409a and bta-miR-378 were significantly down regulated in preovulatory dominant follicles. In-silico pathway analysis revealed that canonical pathways related to oncogenesis, cell adhesion, cell proliferation, apoptosis and metabolism were significantly enriched by the predicted target genes of differentially expressed miRNAs. Furthermore, Luciferase reporter assay analysis showed that one of the differentially regulated miRNAs, the miR-183 cluster miRNAs, were validated to target the 3'-UTR of FOXO1 gene. Moreover FOXO1 was highly enriched in granulosa cells of subordinate follicles in comparison with the preovulatory dominant follicles demonstrating reciprocal expression pattern with miR-183 cluster miRNAs. In conclusion, the presence of distinct sets of miRNAs in granulosa cells of preovulatory dominant and subordinate follicles supports the potential role of miRNAs in post-transcriptional regulation of genes involved in bovine follicular development during the late follicular phase of the estrous cycle. |
doi_str_mv | 10.1371/journal.pone.0125912 |
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The dominant follicle of the follicular wave which coincides with the LH-surge becomes ovulatory, leaving the subordinate follicles to undergo atresia. These physiological processes are controlled by timely and spatially expressed genes and gene products, which in turn are regulated by post-transcriptional regulators. MicroRNAs, a class of short non-coding RNA molecules, are one of the important posttranscriptional regulators of genes associated with various cellular processes. Here we investigated the expression pattern of miRNAs in granulosa cells of bovine preovulatory dominant and subordinate follicles during the late follicular phase of bovine estrous cycle using Illumina miRNA deep sequencing. In addition to 11 putative novel miRNAs, a total of 315 and 323 known miRNAs were detected in preovulatory dominant and subordinate follicles, respectively. Moreover, in comparison with the subordinate follicles, a total of 64 miRNAs were found to be differentially expressed in preovulatory dominant follicles, of which 34 miRNAs including the miR-132 and miR-183 clusters were significantly enriched, and 30 miRNAs including the miR-17-92 cluster, bta-miR-409a and bta-miR-378 were significantly down regulated in preovulatory dominant follicles. In-silico pathway analysis revealed that canonical pathways related to oncogenesis, cell adhesion, cell proliferation, apoptosis and metabolism were significantly enriched by the predicted target genes of differentially expressed miRNAs. Furthermore, Luciferase reporter assay analysis showed that one of the differentially regulated miRNAs, the miR-183 cluster miRNAs, were validated to target the 3'-UTR of FOXO1 gene. Moreover FOXO1 was highly enriched in granulosa cells of subordinate follicles in comparison with the preovulatory dominant follicles demonstrating reciprocal expression pattern with miR-183 cluster miRNAs. In conclusion, the presence of distinct sets of miRNAs in granulosa cells of preovulatory dominant and subordinate follicles supports the potential role of miRNAs in post-transcriptional regulation of genes involved in bovine follicular development during the late follicular phase of the estrous cycle.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0125912</identifier><identifier>PMID: 25993098</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>3' Untranslated regions ; Animal sciences ; Animals ; Apoptosis ; Breeding of animals ; Cancer ; Cattle ; Cell adhesion ; Cell proliferation ; Clusters ; Endocrinology ; Enrichment ; Estrus ; Estrus cycle ; Female ; Follicles ; Follicular Phase ; FOXO1 protein ; Gene expression ; Gene Expression Profiling ; Gene regulation ; Genes ; Granulosa cells ; Granulosa Cells - metabolism ; High-Throughput Nucleotide Sequencing ; Hormones ; Luciferase ; Metabolism ; MicroRNA ; MicroRNAs ; MicroRNAs - genetics ; miRNA ; Non-coding RNA ; Post-transcription ; Ribonucleic acid ; RNA ; Rodents ; Tumorigenesis ; Zoology</subject><ispartof>PloS one, 2015-05, Vol.10 (5), p.e0125912-e0125912</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Gebremedhn et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Gebremedhn et al 2015 Gebremedhn et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-239b7bd9e5ca84a7e547793d48e7b4f1c9aba63b2230481bfdea59242d5b97693</citedby><cites>FETCH-LOGICAL-c692t-239b7bd9e5ca84a7e547793d48e7b4f1c9aba63b2230481bfdea59242d5b97693</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438052/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4438052/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25993098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Zhang, Meijia</contributor><creatorcontrib>Gebremedhn, Samuel</creatorcontrib><creatorcontrib>Salilew-Wondim, Dessie</creatorcontrib><creatorcontrib>Ahmad, Ijaz</creatorcontrib><creatorcontrib>Sahadevan, Sudeep</creatorcontrib><creatorcontrib>Hossain, Md Munir</creatorcontrib><creatorcontrib>Hoelker, Michael</creatorcontrib><creatorcontrib>Rings, Franca</creatorcontrib><creatorcontrib>Neuhoff, Christiane</creatorcontrib><creatorcontrib>Tholen, Ernst</creatorcontrib><creatorcontrib>Looft, Christian</creatorcontrib><creatorcontrib>Schellander, Karl</creatorcontrib><creatorcontrib>Tesfaye, Dawit</creatorcontrib><title>MicroRNA Expression Profile in Bovine Granulosa Cells of Preovulatory Dominant and Subordinate Follicles during the Late Follicular Phase of the Estrous Cycle</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>In bovine, ovarian follicles grow in a wave-like fashion with commonly 2 or 3 follicular waves emerging per estrous cycle. The dominant follicle of the follicular wave which coincides with the LH-surge becomes ovulatory, leaving the subordinate follicles to undergo atresia. These physiological processes are controlled by timely and spatially expressed genes and gene products, which in turn are regulated by post-transcriptional regulators. MicroRNAs, a class of short non-coding RNA molecules, are one of the important posttranscriptional regulators of genes associated with various cellular processes. Here we investigated the expression pattern of miRNAs in granulosa cells of bovine preovulatory dominant and subordinate follicles during the late follicular phase of bovine estrous cycle using Illumina miRNA deep sequencing. In addition to 11 putative novel miRNAs, a total of 315 and 323 known miRNAs were detected in preovulatory dominant and subordinate follicles, respectively. Moreover, in comparison with the subordinate follicles, a total of 64 miRNAs were found to be differentially expressed in preovulatory dominant follicles, of which 34 miRNAs including the miR-132 and miR-183 clusters were significantly enriched, and 30 miRNAs including the miR-17-92 cluster, bta-miR-409a and bta-miR-378 were significantly down regulated in preovulatory dominant follicles. In-silico pathway analysis revealed that canonical pathways related to oncogenesis, cell adhesion, cell proliferation, apoptosis and metabolism were significantly enriched by the predicted target genes of differentially expressed miRNAs. Furthermore, Luciferase reporter assay analysis showed that one of the differentially regulated miRNAs, the miR-183 cluster miRNAs, were validated to target the 3'-UTR of FOXO1 gene. Moreover FOXO1 was highly enriched in granulosa cells of subordinate follicles in comparison with the preovulatory dominant follicles demonstrating reciprocal expression pattern with miR-183 cluster miRNAs. In conclusion, the presence of distinct sets of miRNAs in granulosa cells of preovulatory dominant and subordinate follicles supports the potential role of miRNAs in post-transcriptional regulation of genes involved in bovine follicular development during the late follicular phase of the estrous cycle.</description><subject>3' Untranslated regions</subject><subject>Animal sciences</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Breeding of animals</subject><subject>Cancer</subject><subject>Cattle</subject><subject>Cell adhesion</subject><subject>Cell proliferation</subject><subject>Clusters</subject><subject>Endocrinology</subject><subject>Enrichment</subject><subject>Estrus</subject><subject>Estrus cycle</subject><subject>Female</subject><subject>Follicles</subject><subject>Follicular Phase</subject><subject>FOXO1 protein</subject><subject>Gene expression</subject><subject>Gene Expression Profiling</subject><subject>Gene 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Expression Profile in Bovine Granulosa Cells of Preovulatory Dominant and Subordinate Follicles during the Late Follicular Phase of the Estrous Cycle</title><author>Gebremedhn, Samuel ; Salilew-Wondim, Dessie ; Ahmad, Ijaz ; Sahadevan, Sudeep ; Hossain, Md Munir ; Hoelker, Michael ; Rings, Franca ; Neuhoff, Christiane ; Tholen, Ernst ; Looft, Christian ; Schellander, Karl ; Tesfaye, Dawit</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-239b7bd9e5ca84a7e547793d48e7b4f1c9aba63b2230481bfdea59242d5b97693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>3' Untranslated regions</topic><topic>Animal sciences</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Breeding of animals</topic><topic>Cancer</topic><topic>Cattle</topic><topic>Cell adhesion</topic><topic>Cell 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One</addtitle><date>2015-05-19</date><risdate>2015</risdate><volume>10</volume><issue>5</issue><spage>e0125912</spage><epage>e0125912</epage><pages>e0125912-e0125912</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>In bovine, ovarian follicles grow in a wave-like fashion with commonly 2 or 3 follicular waves emerging per estrous cycle. The dominant follicle of the follicular wave which coincides with the LH-surge becomes ovulatory, leaving the subordinate follicles to undergo atresia. These physiological processes are controlled by timely and spatially expressed genes and gene products, which in turn are regulated by post-transcriptional regulators. MicroRNAs, a class of short non-coding RNA molecules, are one of the important posttranscriptional regulators of genes associated with various cellular processes. Here we investigated the expression pattern of miRNAs in granulosa cells of bovine preovulatory dominant and subordinate follicles during the late follicular phase of bovine estrous cycle using Illumina miRNA deep sequencing. In addition to 11 putative novel miRNAs, a total of 315 and 323 known miRNAs were detected in preovulatory dominant and subordinate follicles, respectively. Moreover, in comparison with the subordinate follicles, a total of 64 miRNAs were found to be differentially expressed in preovulatory dominant follicles, of which 34 miRNAs including the miR-132 and miR-183 clusters were significantly enriched, and 30 miRNAs including the miR-17-92 cluster, bta-miR-409a and bta-miR-378 were significantly down regulated in preovulatory dominant follicles. In-silico pathway analysis revealed that canonical pathways related to oncogenesis, cell adhesion, cell proliferation, apoptosis and metabolism were significantly enriched by the predicted target genes of differentially expressed miRNAs. Furthermore, Luciferase reporter assay analysis showed that one of the differentially regulated miRNAs, the miR-183 cluster miRNAs, were validated to target the 3'-UTR of FOXO1 gene. Moreover FOXO1 was highly enriched in granulosa cells of subordinate follicles in comparison with the preovulatory dominant follicles demonstrating reciprocal expression pattern with miR-183 cluster miRNAs. In conclusion, the presence of distinct sets of miRNAs in granulosa cells of preovulatory dominant and subordinate follicles supports the potential role of miRNAs in post-transcriptional regulation of genes involved in bovine follicular development during the late follicular phase of the estrous cycle.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25993098</pmid><doi>10.1371/journal.pone.0125912</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2015-05, Vol.10 (5), p.e0125912-e0125912 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1681916337 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS) Journals Open Access; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | 3' Untranslated regions Animal sciences Animals Apoptosis Breeding of animals Cancer Cattle Cell adhesion Cell proliferation Clusters Endocrinology Enrichment Estrus Estrus cycle Female Follicles Follicular Phase FOXO1 protein Gene expression Gene Expression Profiling Gene regulation Genes Granulosa cells Granulosa Cells - metabolism High-Throughput Nucleotide Sequencing Hormones Luciferase Metabolism MicroRNA MicroRNAs MicroRNAs - genetics miRNA Non-coding RNA Post-transcription Ribonucleic acid RNA Rodents Tumorigenesis Zoology |
title | MicroRNA Expression Profile in Bovine Granulosa Cells of Preovulatory Dominant and Subordinate Follicles during the Late Follicular Phase of the Estrous Cycle |
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