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Progesterone receptor-dependent regulation of genes in the oviducts of female mice
Oviducts play a critical role in gamete and embryo transport, as well as supporting early embryo development. Progesterone receptor (PGR) is a transcription factor highly expressed in oviductal cells, while its activating ligand, progesterone, surges to peak levels as ovulation approaches. Progester...
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Published in: | Physiological genomics 2014-08, Vol.46 (16), p.583-592 |
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creator | Akison, Lisa K Boden, Michael J Kennaway, David J Russell, Darryl L Robker, Rebecca L |
description | Oviducts play a critical role in gamete and embryo transport, as well as supporting early embryo development. Progesterone receptor (PGR) is a transcription factor highly expressed in oviductal cells, while its activating ligand, progesterone, surges to peak levels as ovulation approaches. Progesterone is known to regulate oviduct cilia beating and muscular contractions in vitro, but how PGR may mediate this in vivo is poorly understood. We used PGR null mice to identify genes potentially regulated by PGR in the oviducts during the periovulatory period. Histologically, oviducts from PGR null mice showed no gross structural or morphological defects compared with normal littermates. However, microarray analysis of oviducts at 8 h posthuman chorionic gonadotropin revealed >1,000 PGR-dependent genes. Using reverse-transcription polymerase chain reaction (RT-PCR) we selected 10 genes for validation based on their potential roles in oocyte/embryo transport and support. Eight genes were confirmed to be downregulated (Adamts1, Itga8, Edn3, Prlr, Ptgfr, Des, Myocd, and Actg2) and one upregulated (Agtr2) in PGR null oviducts. Expression of these genes was also assessed in oviducts of naturally cycling mice during ovulation and day 1 and day 4 of pregnancy. Adamts1, Itga8, Edn3, Prlr, and Ptgfr were significantly upregulated in oviducts at ovulation/mating. However, most genes showed basal levels of expression at other times. The exceptions were Prlr and Ptgfr, which showed pulsatile increases on day 1 and/or day 4 of pregnancy. This is the first, comprehensive study to elucidate putative PGR-regulated genes in the oviduct and reveals key downstream targets potentially mediating oocyte and embryo transport. |
doi_str_mv | 10.1152/physiolgenomics.00044.2014 |
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Progesterone receptor (PGR) is a transcription factor highly expressed in oviductal cells, while its activating ligand, progesterone, surges to peak levels as ovulation approaches. Progesterone is known to regulate oviduct cilia beating and muscular contractions in vitro, but how PGR may mediate this in vivo is poorly understood. We used PGR null mice to identify genes potentially regulated by PGR in the oviducts during the periovulatory period. Histologically, oviducts from PGR null mice showed no gross structural or morphological defects compared with normal littermates. However, microarray analysis of oviducts at 8 h posthuman chorionic gonadotropin revealed >1,000 PGR-dependent genes. Using reverse-transcription polymerase chain reaction (RT-PCR) we selected 10 genes for validation based on their potential roles in oocyte/embryo transport and support. Eight genes were confirmed to be downregulated (Adamts1, Itga8, Edn3, Prlr, Ptgfr, Des, Myocd, and Actg2) and one upregulated (Agtr2) in PGR null oviducts. Expression of these genes was also assessed in oviducts of naturally cycling mice during ovulation and day 1 and day 4 of pregnancy. Adamts1, Itga8, Edn3, Prlr, and Ptgfr were significantly upregulated in oviducts at ovulation/mating. However, most genes showed basal levels of expression at other times. The exceptions were Prlr and Ptgfr, which showed pulsatile increases on day 1 and/or day 4 of pregnancy. 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Progesterone receptor (PGR) is a transcription factor highly expressed in oviductal cells, while its activating ligand, progesterone, surges to peak levels as ovulation approaches. Progesterone is known to regulate oviduct cilia beating and muscular contractions in vitro, but how PGR may mediate this in vivo is poorly understood. We used PGR null mice to identify genes potentially regulated by PGR in the oviducts during the periovulatory period. Histologically, oviducts from PGR null mice showed no gross structural or morphological defects compared with normal littermates. However, microarray analysis of oviducts at 8 h posthuman chorionic gonadotropin revealed >1,000 PGR-dependent genes. Using reverse-transcription polymerase chain reaction (RT-PCR) we selected 10 genes for validation based on their potential roles in oocyte/embryo transport and support. Eight genes were confirmed to be downregulated (Adamts1, Itga8, Edn3, Prlr, Ptgfr, Des, Myocd, and Actg2) and one upregulated (Agtr2) in PGR null oviducts. Expression of these genes was also assessed in oviducts of naturally cycling mice during ovulation and day 1 and day 4 of pregnancy. Adamts1, Itga8, Edn3, Prlr, and Ptgfr were significantly upregulated in oviducts at ovulation/mating. However, most genes showed basal levels of expression at other times. The exceptions were Prlr and Ptgfr, which showed pulsatile increases on day 1 and/or day 4 of pregnancy. This is the first, comprehensive study to elucidate putative PGR-regulated genes in the oviduct and reveals key downstream targets potentially mediating oocyte and embryo transport.</description><subject>Animals</subject><subject>Chorionic Gonadotropin - pharmacology</subject><subject>Embryonic Development - genetics</subject><subject>Female</subject><subject>Gene Expression Profiling - methods</subject><subject>Gene Expression Regulation, Developmental - drug effects</subject><subject>Horses</subject><subject>Humans</subject><subject>Male</subject><subject>Mice, 129 Strain</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Oviducts - metabolism</subject><subject>Ovulation - genetics</subject><subject>Pregnancy</subject><subject>Receptors, Progesterone - genetics</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><issn>1094-8341</issn><issn>1531-2267</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAMgCMEYuPxF1DFiUtHnk3KDU28pEkgtHvUJc5W1DYlaZH492RscODCyZH9ObY_hC4JnhEi6HW_-Yy1b9bQ-bY2cYYx5nxGMeEHaEoEIzmlhTxMb1zyXDFOJugkxjecCKnEMZpQXpKiLNQUvb4Ev4Y4QPAdZAEM9IMPuYUeOgvdkFLrsamG2neZd1maCTGru2zYQOY_ajuaIW4LDtqqgSztA2foyFVNhPN9PEXL-7vl_DFfPD88zW8XueFEDbnAyjpaUWYtIaTE4KjltixloagwjAtViBVTCZOWAlPOMYpLqRQYacyKnaKr3bd98O9jOkG3dTTQNFUHfoyaFJKxkkhe_I8KwbnkmKiE3uxQE3yMAZzuQ91W4VMTrLf29R_7-tu-3tpPzRf7OeOqBfvb-qObfQFemYXk</recordid><startdate>20140815</startdate><enddate>20140815</enddate><creator>Akison, Lisa K</creator><creator>Boden, Michael J</creator><creator>Kennaway, David J</creator><creator>Russell, Darryl L</creator><creator>Robker, Rebecca L</creator><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>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20140815</creationdate><title>Progesterone receptor-dependent regulation of genes in the oviducts of female mice</title><author>Akison, Lisa K ; Boden, Michael J ; Kennaway, David J ; Russell, Darryl L ; Robker, Rebecca L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-508df2a23dd11190ef2d4d9976825c345865b385087d2e38ff3209788ec7ccb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Chorionic Gonadotropin - pharmacology</topic><topic>Embryonic Development - genetics</topic><topic>Female</topic><topic>Gene Expression Profiling - methods</topic><topic>Gene Expression Regulation, Developmental - drug effects</topic><topic>Horses</topic><topic>Humans</topic><topic>Male</topic><topic>Mice, 129 Strain</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Mice, Transgenic</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Oviducts - metabolism</topic><topic>Ovulation - genetics</topic><topic>Pregnancy</topic><topic>Receptors, Progesterone - genetics</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Akison, Lisa K</creatorcontrib><creatorcontrib>Boden, Michael J</creatorcontrib><creatorcontrib>Kennaway, David J</creatorcontrib><creatorcontrib>Russell, Darryl L</creatorcontrib><creatorcontrib>Robker, Rebecca L</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Physiological genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Akison, Lisa K</au><au>Boden, Michael J</au><au>Kennaway, David J</au><au>Russell, Darryl L</au><au>Robker, Rebecca L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progesterone receptor-dependent regulation of genes in the oviducts of female mice</atitle><jtitle>Physiological genomics</jtitle><addtitle>Physiol Genomics</addtitle><date>2014-08-15</date><risdate>2014</risdate><volume>46</volume><issue>16</issue><spage>583</spage><epage>592</epage><pages>583-592</pages><issn>1094-8341</issn><eissn>1531-2267</eissn><abstract>Oviducts play a critical role in gamete and embryo transport, as well as supporting early embryo development. Progesterone receptor (PGR) is a transcription factor highly expressed in oviductal cells, while its activating ligand, progesterone, surges to peak levels as ovulation approaches. Progesterone is known to regulate oviduct cilia beating and muscular contractions in vitro, but how PGR may mediate this in vivo is poorly understood. We used PGR null mice to identify genes potentially regulated by PGR in the oviducts during the periovulatory period. Histologically, oviducts from PGR null mice showed no gross structural or morphological defects compared with normal littermates. However, microarray analysis of oviducts at 8 h posthuman chorionic gonadotropin revealed >1,000 PGR-dependent genes. Using reverse-transcription polymerase chain reaction (RT-PCR) we selected 10 genes for validation based on their potential roles in oocyte/embryo transport and support. Eight genes were confirmed to be downregulated (Adamts1, Itga8, Edn3, Prlr, Ptgfr, Des, Myocd, and Actg2) and one upregulated (Agtr2) in PGR null oviducts. Expression of these genes was also assessed in oviducts of naturally cycling mice during ovulation and day 1 and day 4 of pregnancy. Adamts1, Itga8, Edn3, Prlr, and Ptgfr were significantly upregulated in oviducts at ovulation/mating. However, most genes showed basal levels of expression at other times. The exceptions were Prlr and Ptgfr, which showed pulsatile increases on day 1 and/or day 4 of pregnancy. This is the first, comprehensive study to elucidate putative PGR-regulated genes in the oviduct and reveals key downstream targets potentially mediating oocyte and embryo transport.</abstract><cop>United States</cop><pmid>24916968</pmid><doi>10.1152/physiolgenomics.00044.2014</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Chorionic Gonadotropin - pharmacology Embryonic Development - genetics Female Gene Expression Profiling - methods Gene Expression Regulation, Developmental - drug effects Horses Humans Male Mice, 129 Strain Mice, Inbred C57BL Mice, Knockout Mice, Transgenic Oligonucleotide Array Sequence Analysis Oviducts - metabolism Ovulation - genetics Pregnancy Receptors, Progesterone - genetics Reverse Transcriptase Polymerase Chain Reaction |
title | Progesterone receptor-dependent regulation of genes in the oviducts of female mice |
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