Evaluation of circulating miRNAs during late pregnancy in the mare
MicroRNAs (miRNAs) are small, non-coding RNAs which are produced throughout the body. Individual tissues tend to have a specific expression profile and excrete many of these miRNAs into circulation. These circulating miRNAs may be diagnostically valuable biomarkers for assessing the presence of dise...
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description | MicroRNAs (miRNAs) are small, non-coding RNAs which are produced throughout the body. Individual tissues tend to have a specific expression profile and excrete many of these miRNAs into circulation. These circulating miRNAs may be diagnostically valuable biomarkers for assessing the presence of disease while minimizing invasive testing. In women, numerous circulating miRNAs have been identified which change significantly during pregnancy-related complications (e.g. chorioamnionitis, eclampsia, recurrent pregnancy loss); however, no prior work has been done in this area in the horse. To identify pregnancy-specific miRNAs, we collected serial whole blood samples in pregnant mares at 8, 9, 10 m of gestation and post-partum, as well as from non-pregnant (diestrous) mares. In total, we evaluated a panel of 178 miRNAs using qPCR, eventually identifying five miRNAs of interest. One miRNA (miR-374b) was differentially regulated through late gestation and four miRNAs (miR-454, miR-133b, miR-486-5p and miR-204b) were differentially regulated between the pregnant and non-pregnant samples. We were able to identify putative targets for the differentially regulated miRNAs using two separate target prediction programs, miRDB and Ingenuity Pathway Analysis. The targets for the miRNAs differentially regulated during pregnancy were predicted to be involved in signaling pathways such as the STAT3 pathway and PI3/AKT signaling pathway, as well as more endocrine-based pathways, including the GnRH, prolactin and insulin signaling pathways. In summary, this study provides novel information about the changes occurring in circulating miRNAs during normal pregnancy, as well as attempting to predict the biological effects induced by these miRNAs. |
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Individual tissues tend to have a specific expression profile and excrete many of these miRNAs into circulation. These circulating miRNAs may be diagnostically valuable biomarkers for assessing the presence of disease while minimizing invasive testing. In women, numerous circulating miRNAs have been identified which change significantly during pregnancy-related complications (e.g. chorioamnionitis, eclampsia, recurrent pregnancy loss); however, no prior work has been done in this area in the horse. To identify pregnancy-specific miRNAs, we collected serial whole blood samples in pregnant mares at 8, 9, 10 m of gestation and post-partum, as well as from non-pregnant (diestrous) mares. In total, we evaluated a panel of 178 miRNAs using qPCR, eventually identifying five miRNAs of interest. One miRNA (miR-374b) was differentially regulated through late gestation and four miRNAs (miR-454, miR-133b, miR-486-5p and miR-204b) were differentially regulated between the pregnant and non-pregnant samples. We were able to identify putative targets for the differentially regulated miRNAs using two separate target prediction programs, miRDB and Ingenuity Pathway Analysis. The targets for the miRNAs differentially regulated during pregnancy were predicted to be involved in signaling pathways such as the STAT3 pathway and PI3/AKT signaling pathway, as well as more endocrine-based pathways, including the GnRH, prolactin and insulin signaling pathways. In summary, this study provides novel information about the changes occurring in circulating miRNAs during normal pregnancy, as well as attempting to predict the biological effects induced by these miRNAs.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0175045</identifier><identifier>PMID: 28388652</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abortion ; AKT protein ; Analysis ; Animal reproduction ; Animals ; Biological effects ; Biology and life sciences ; Biomarkers ; Chorioamnionitis ; Circulation ; Complications ; Computer and Information Sciences ; Eclampsia ; Female ; Gene expression ; Gestation ; Gonadotropin-releasing hormone ; Health aspects ; Horses ; Insulin ; Medicine and Health Sciences ; MicroRNA ; MicroRNAs ; MicroRNAs - blood ; miRNA ; Miscarriage ; Predictions ; Pregnancy ; Pregnancy complications ; Pregnancy, Animal - blood ; Prolactin ; Protein expression ; Reverse Transcriptase Polymerase Chain Reaction ; Signal transduction ; Stat3 protein ; Target recognition ; Tissues</subject><ispartof>PloS one, 2017-04, Vol.12 (4), p.e0175045-e0175045</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Loux 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>2017 Loux et al 2017 Loux et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-e9d10ccbed19ee2920995a19915fa4637dd575ce4b5ee9e0a97277ff5cade59d3</citedby><cites>FETCH-LOGICAL-c692t-e9d10ccbed19ee2920995a19915fa4637dd575ce4b5ee9e0a97277ff5cade59d3</cites><orcidid>0000-0001-5193-6675 ; 0000-0002-0502-0276</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384662/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384662/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2106,2932,23875,27933,27934,53800,53802</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28388652$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Hansen, Peter J.</contributor><creatorcontrib>Loux, Shavahn C</creatorcontrib><creatorcontrib>Scoggin, Kirsten E</creatorcontrib><creatorcontrib>Bruemmer, Jason E</creatorcontrib><creatorcontrib>Canisso, Igor F</creatorcontrib><creatorcontrib>Troedsson, Mats H T</creatorcontrib><creatorcontrib>Squires, Edward L</creatorcontrib><creatorcontrib>Ball, Barry A</creatorcontrib><title>Evaluation of circulating miRNAs during late pregnancy in the mare</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>MicroRNAs (miRNAs) are small, non-coding RNAs which are produced throughout the body. Individual tissues tend to have a specific expression profile and excrete many of these miRNAs into circulation. These circulating miRNAs may be diagnostically valuable biomarkers for assessing the presence of disease while minimizing invasive testing. In women, numerous circulating miRNAs have been identified which change significantly during pregnancy-related complications (e.g. chorioamnionitis, eclampsia, recurrent pregnancy loss); however, no prior work has been done in this area in the horse. To identify pregnancy-specific miRNAs, we collected serial whole blood samples in pregnant mares at 8, 9, 10 m of gestation and post-partum, as well as from non-pregnant (diestrous) mares. In total, we evaluated a panel of 178 miRNAs using qPCR, eventually identifying five miRNAs of interest. One miRNA (miR-374b) was differentially regulated through late gestation and four miRNAs (miR-454, miR-133b, miR-486-5p and miR-204b) were differentially regulated between the pregnant and non-pregnant samples. We were able to identify putative targets for the differentially regulated miRNAs using two separate target prediction programs, miRDB and Ingenuity Pathway Analysis. The targets for the miRNAs differentially regulated during pregnancy were predicted to be involved in signaling pathways such as the STAT3 pathway and PI3/AKT signaling pathway, as well as more endocrine-based pathways, including the GnRH, prolactin and insulin signaling pathways. In summary, this study provides novel information about the changes occurring in circulating miRNAs during normal pregnancy, as well as attempting to predict the biological effects induced by these miRNAs.</description><subject>Abortion</subject><subject>AKT protein</subject><subject>Analysis</subject><subject>Animal reproduction</subject><subject>Animals</subject><subject>Biological effects</subject><subject>Biology and life sciences</subject><subject>Biomarkers</subject><subject>Chorioamnionitis</subject><subject>Circulation</subject><subject>Complications</subject><subject>Computer and Information Sciences</subject><subject>Eclampsia</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gestation</subject><subject>Gonadotropin-releasing hormone</subject><subject>Health aspects</subject><subject>Horses</subject><subject>Insulin</subject><subject>Medicine and Health Sciences</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - blood</subject><subject>miRNA</subject><subject>Miscarriage</subject><subject>Predictions</subject><subject>Pregnancy</subject><subject>Pregnancy complications</subject><subject>Pregnancy, Animal - blood</subject><subject>Prolactin</subject><subject>Protein expression</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Signal transduction</subject><subject>Stat3 protein</subject><subject>Target recognition</subject><subject>Tissues</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1v0zAUhiMEYh_wDxBEQkJw0WI7sWPfIJVpQKWJSePj1nLtk9SVG3d2Mm3_HodmU4N2wZXjk-e858Nvlr3CaI6LCn_c-D60ys13voU5whVFJX2SHWNRkBkjqHh68H2UncS4QYgWnLHn2RHhBeeMkuPs8_mNcr3qrG9zX-faBt27dG2bfGuvvi9ibvow3FIQ8l2AplWtvsttm3dryLcqwIvsWa1chJfjeZr9-nL-8-zb7OLy6_JscTHTTJBuBsJgpPUKDBYARBAkBFVYCExrVbKiMoZWVEO5ogACkBIVqaq6ploZoMIUp9mbve7O-SjH8aPEnFNCOC9oIpZ7wni1kbtgU3t30isr_wZ8aKQKndUOJCqAlIhipo0u61IrzUyN8IqiukSkgqT1aazWr7ZgNLRdUG4iOv3T2rVs_I1MOy4ZI0ng_SgQ_HUPsZNbGzU4p1rw_b5vUVLKhr7f_oM-Pt1INSoNYNvap7p6EJWLknOOCKVD2fkjlBqWuLU6eaW2KT5J-DBJSEwHt12j-hjl8sfV_7OXv6fsuwN2Dcp16-hdP1gtTsFyD-rgYwxQPywZIzlY_X4bcrC6HK2e0l4fPtBD0r23iz8KcPiU</recordid><startdate>20170407</startdate><enddate>20170407</enddate><creator>Loux, Shavahn C</creator><creator>Scoggin, Kirsten E</creator><creator>Bruemmer, Jason E</creator><creator>Canisso, Igor F</creator><creator>Troedsson, Mats H T</creator><creator>Squires, Edward L</creator><creator>Ball, Barry A</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-5193-6675</orcidid><orcidid>https://orcid.org/0000-0002-0502-0276</orcidid></search><sort><creationdate>20170407</creationdate><title>Evaluation of circulating miRNAs during late pregnancy in the mare</title><author>Loux, Shavahn C ; Scoggin, Kirsten E ; Bruemmer, Jason E ; Canisso, Igor F ; Troedsson, Mats H T ; Squires, Edward L ; Ball, Barry A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-e9d10ccbed19ee2920995a19915fa4637dd575ce4b5ee9e0a97277ff5cade59d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Abortion</topic><topic>AKT protein</topic><topic>Analysis</topic><topic>Animal reproduction</topic><topic>Animals</topic><topic>Biological effects</topic><topic>Biology and life sciences</topic><topic>Biomarkers</topic><topic>Chorioamnionitis</topic><topic>Circulation</topic><topic>Complications</topic><topic>Computer and Information Sciences</topic><topic>Eclampsia</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gestation</topic><topic>Gonadotropin-releasing hormone</topic><topic>Health aspects</topic><topic>Horses</topic><topic>Insulin</topic><topic>Medicine and Health Sciences</topic><topic>MicroRNA</topic><topic>MicroRNAs</topic><topic>MicroRNAs - blood</topic><topic>miRNA</topic><topic>Miscarriage</topic><topic>Predictions</topic><topic>Pregnancy</topic><topic>Pregnancy complications</topic><topic>Pregnancy, Animal - blood</topic><topic>Prolactin</topic><topic>Protein expression</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Signal transduction</topic><topic>Stat3 protein</topic><topic>Target recognition</topic><topic>Tissues</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Loux, Shavahn C</creatorcontrib><creatorcontrib>Scoggin, Kirsten E</creatorcontrib><creatorcontrib>Bruemmer, Jason E</creatorcontrib><creatorcontrib>Canisso, Igor F</creatorcontrib><creatorcontrib>Troedsson, Mats H T</creatorcontrib><creatorcontrib>Squires, Edward L</creatorcontrib><creatorcontrib>Ball, Barry A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Loux, Shavahn C</au><au>Scoggin, Kirsten E</au><au>Bruemmer, Jason E</au><au>Canisso, Igor F</au><au>Troedsson, Mats H T</au><au>Squires, Edward L</au><au>Ball, Barry A</au><au>Hansen, Peter J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of circulating miRNAs during late pregnancy in the mare</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-04-07</date><risdate>2017</risdate><volume>12</volume><issue>4</issue><spage>e0175045</spage><epage>e0175045</epage><pages>e0175045-e0175045</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>MicroRNAs (miRNAs) are small, non-coding RNAs which are produced throughout the body. Individual tissues tend to have a specific expression profile and excrete many of these miRNAs into circulation. These circulating miRNAs may be diagnostically valuable biomarkers for assessing the presence of disease while minimizing invasive testing. In women, numerous circulating miRNAs have been identified which change significantly during pregnancy-related complications (e.g. chorioamnionitis, eclampsia, recurrent pregnancy loss); however, no prior work has been done in this area in the horse. To identify pregnancy-specific miRNAs, we collected serial whole blood samples in pregnant mares at 8, 9, 10 m of gestation and post-partum, as well as from non-pregnant (diestrous) mares. In total, we evaluated a panel of 178 miRNAs using qPCR, eventually identifying five miRNAs of interest. One miRNA (miR-374b) was differentially regulated through late gestation and four miRNAs (miR-454, miR-133b, miR-486-5p and miR-204b) were differentially regulated between the pregnant and non-pregnant samples. We were able to identify putative targets for the differentially regulated miRNAs using two separate target prediction programs, miRDB and Ingenuity Pathway Analysis. The targets for the miRNAs differentially regulated during pregnancy were predicted to be involved in signaling pathways such as the STAT3 pathway and PI3/AKT signaling pathway, as well as more endocrine-based pathways, including the GnRH, prolactin and insulin signaling pathways. In summary, this study provides novel information about the changes occurring in circulating miRNAs during normal pregnancy, as well as attempting to predict the biological effects induced by these miRNAs.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28388652</pmid><doi>10.1371/journal.pone.0175045</doi><tpages>e0175045</tpages><orcidid>https://orcid.org/0000-0001-5193-6675</orcidid><orcidid>https://orcid.org/0000-0002-0502-0276</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abortion AKT protein Analysis Animal reproduction Animals Biological effects Biology and life sciences Biomarkers Chorioamnionitis Circulation Complications Computer and Information Sciences Eclampsia Female Gene expression Gestation Gonadotropin-releasing hormone Health aspects Horses Insulin Medicine and Health Sciences MicroRNA MicroRNAs MicroRNAs - blood miRNA Miscarriage Predictions Pregnancy Pregnancy complications Pregnancy, Animal - blood Prolactin Protein expression Reverse Transcriptase Polymerase Chain Reaction Signal transduction Stat3 protein Target recognition Tissues |
title | Evaluation of circulating miRNAs during late pregnancy in the mare |
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