Transcriptional activation of elephant shark mineralocorticoid receptor by corticosteroids, progesterone, and spironolactone
The mineralocorticoid receptor (MR) is a nuclear receptor and part of a large and diverse family of transcription factors that also includes receptors for glucocorticoids, progesterone, androgens, and estrogens. The corticosteroid aldosterone is the physiological activator of the MR in humans and ot...
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description | The mineralocorticoid receptor (MR) is a nuclear receptor and part of a large and diverse family of transcription factors that also includes receptors for glucocorticoids, progesterone, androgens, and estrogens. The corticosteroid aldosterone is the physiological activator of the MR in humans and other terrestrial vertebrates; however, its activator is not known in cartilaginous fish, the oldest group of extant jawed vertebrates. Here, we analyzed the ability of corticosteroids and progesterone to activate the full-length MR from the elephant shark (
). On the basis of their measured activities, aldosterone, cortisol, 11-deoxycorticosterone, corticosterone, 11-deoxcortisol, progesterone, and 19-norprogesterone are potential physiological mineralocorticoids. However, aldosterone, the physiological mineralocorticoid in humans and other terrestrial vertebrates, is not found in cartilaginous or ray-finned fish. Although progesterone activates MRs in ray-finned fish, progesterone does not activate MRs in humans, amphibians, or alligator, suggesting that during the transition to terrestrial vertebrates, progesterone lost the ability to activate the MR. Both elephant shark MR and human MR are expressed in the brain, heart, ovary, testis, and other nonepithelial tissues, suggesting that MR expression in diverse tissues evolved in the common ancestor of jawed vertebrates. Our data suggest that 19-norprogesterone- and progesterone-activated MR may have unappreciated functions in reproductive physiology. |
doi_str_mv | 10.1126/scisignal.aar2668 |
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). On the basis of their measured activities, aldosterone, cortisol, 11-deoxycorticosterone, corticosterone, 11-deoxcortisol, progesterone, and 19-norprogesterone are potential physiological mineralocorticoids. However, aldosterone, the physiological mineralocorticoid in humans and other terrestrial vertebrates, is not found in cartilaginous or ray-finned fish. Although progesterone activates MRs in ray-finned fish, progesterone does not activate MRs in humans, amphibians, or alligator, suggesting that during the transition to terrestrial vertebrates, progesterone lost the ability to activate the MR. Both elephant shark MR and human MR are expressed in the brain, heart, ovary, testis, and other nonepithelial tissues, suggesting that MR expression in diverse tissues evolved in the common ancestor of jawed vertebrates. Our data suggest that 19-norprogesterone- and progesterone-activated MR may have unappreciated functions in reproductive physiology.</description><identifier>ISSN: 1945-0877</identifier><identifier>EISSN: 1937-9145</identifier><identifier>DOI: 10.1126/scisignal.aar2668</identifier><identifier>PMID: 31164478</identifier><language>eng</language><publisher>United States: The American Association for the Advancement of Science</publisher><subject>Aldosterone ; Amphibians ; Androgens ; Aquatic reptiles ; Brain ; Corticoids ; Corticosteroids ; Corticosterone ; Cortisol ; Estrogens ; Fish ; Glucocorticoids ; Homeostasis ; Hormones ; Mineralocorticoid receptors ; Ovaries ; Physiological effects ; Physiology ; Progesterone ; Receptors ; Sharks ; Steroid hormones ; Steroids ; Terrestrial environments ; Transcription activation ; Transcription factors ; Vertebrates</subject><ispartof>Science signaling, 2019-06, Vol.12 (584)</ispartof><rights>Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.</rights><rights>Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-102ccb1cd4182404a03256b793642a9ea79f8aefe7d784e72fb33fc56a24e5ac3</citedby><cites>FETCH-LOGICAL-c438t-102ccb1cd4182404a03256b793642a9ea79f8aefe7d784e72fb33fc56a24e5ac3</cites><orcidid>0000-0001-6184-3616 ; 0000-0002-8084-8145 ; 0000-0003-4387-3269 ; 0000-0003-2625-4626 ; 0000-0002-7882-0223 ; 0000-0003-2024-6721</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2870,2871,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31164478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Katsu, Yoshinao</creatorcontrib><creatorcontrib>Kohno, Satomi</creatorcontrib><creatorcontrib>Oka, Kaori</creatorcontrib><creatorcontrib>Lin, Xiaozhi</creatorcontrib><creatorcontrib>Otake, Sumika</creatorcontrib><creatorcontrib>Pillai, Nisha E</creatorcontrib><creatorcontrib>Takagi, Wataru</creatorcontrib><creatorcontrib>Hyodo, Susumu</creatorcontrib><creatorcontrib>Venkatesh, Byrappa</creatorcontrib><creatorcontrib>Baker, Michael E</creatorcontrib><title>Transcriptional activation of elephant shark mineralocorticoid receptor by corticosteroids, progesterone, and spironolactone</title><title>Science signaling</title><addtitle>Sci Signal</addtitle><description>The mineralocorticoid receptor (MR) is a nuclear receptor and part of a large and diverse family of transcription factors that also includes receptors for glucocorticoids, progesterone, androgens, and estrogens. The corticosteroid aldosterone is the physiological activator of the MR in humans and other terrestrial vertebrates; however, its activator is not known in cartilaginous fish, the oldest group of extant jawed vertebrates. Here, we analyzed the ability of corticosteroids and progesterone to activate the full-length MR from the elephant shark (
). On the basis of their measured activities, aldosterone, cortisol, 11-deoxycorticosterone, corticosterone, 11-deoxcortisol, progesterone, and 19-norprogesterone are potential physiological mineralocorticoids. However, aldosterone, the physiological mineralocorticoid in humans and other terrestrial vertebrates, is not found in cartilaginous or ray-finned fish. Although progesterone activates MRs in ray-finned fish, progesterone does not activate MRs in humans, amphibians, or alligator, suggesting that during the transition to terrestrial vertebrates, progesterone lost the ability to activate the MR. Both elephant shark MR and human MR are expressed in the brain, heart, ovary, testis, and other nonepithelial tissues, suggesting that MR expression in diverse tissues evolved in the common ancestor of jawed vertebrates. Our data suggest that 19-norprogesterone- and progesterone-activated MR may have unappreciated functions in reproductive physiology.</description><subject>Aldosterone</subject><subject>Amphibians</subject><subject>Androgens</subject><subject>Aquatic reptiles</subject><subject>Brain</subject><subject>Corticoids</subject><subject>Corticosteroids</subject><subject>Corticosterone</subject><subject>Cortisol</subject><subject>Estrogens</subject><subject>Fish</subject><subject>Glucocorticoids</subject><subject>Homeostasis</subject><subject>Hormones</subject><subject>Mineralocorticoid receptors</subject><subject>Ovaries</subject><subject>Physiological effects</subject><subject>Physiology</subject><subject>Progesterone</subject><subject>Receptors</subject><subject>Sharks</subject><subject>Steroid hormones</subject><subject>Steroids</subject><subject>Terrestrial environments</subject><subject>Transcription activation</subject><subject>Transcription factors</subject><subject>Vertebrates</subject><issn>1945-0877</issn><issn>1937-9145</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpdkctOwzAQRS0EglL4ADbIEhsWBPyKnSwR4iUhsSnraOJMWkMaBztFQuLjcaF0wcq-4zPXo7mEnHB2ybnQV9G66OY9dJcAQWhd7JAJL6XJSq7y3fVd5RkrjDkghzG-Mqa5EOU-OZCca6VMMSFfswB9tMENo_PJiYId3QesBfUtxQ6HBfQjjQsIb3TpegzQeevD6Kx3DQ1ocRh9oPUn3VTjiCE9xQs6BD_HH9njBYW-oXFwSfgu_ZJqR2SvhS7i8eackpe729nNQ_b0fP94c_2UWSWLMeNMWFtz2yheCMUUMClyXZtSaiWgRDBlWwC2aBpTKDSiraVsba5BKMzByik5__VNA72v0kTV0kWLXQc9-lWshFSMKVXkOqFn_9BXvwppMYkSUvNSp9Umiv9SNvgYA7bVENwSwmfFWbWOptpGU22iST2nG-dVvcRm2_GXhfwGdT6RAw</recordid><startdate>20190604</startdate><enddate>20190604</enddate><creator>Katsu, Yoshinao</creator><creator>Kohno, Satomi</creator><creator>Oka, Kaori</creator><creator>Lin, Xiaozhi</creator><creator>Otake, Sumika</creator><creator>Pillai, Nisha E</creator><creator>Takagi, Wataru</creator><creator>Hyodo, Susumu</creator><creator>Venkatesh, Byrappa</creator><creator>Baker, Michael E</creator><general>The American Association for the Advancement of Science</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JQ2</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6184-3616</orcidid><orcidid>https://orcid.org/0000-0002-8084-8145</orcidid><orcidid>https://orcid.org/0000-0003-4387-3269</orcidid><orcidid>https://orcid.org/0000-0003-2625-4626</orcidid><orcidid>https://orcid.org/0000-0002-7882-0223</orcidid><orcidid>https://orcid.org/0000-0003-2024-6721</orcidid></search><sort><creationdate>20190604</creationdate><title>Transcriptional activation of elephant shark mineralocorticoid receptor by corticosteroids, progesterone, and spironolactone</title><author>Katsu, Yoshinao ; Kohno, Satomi ; Oka, Kaori ; Lin, Xiaozhi ; Otake, Sumika ; Pillai, Nisha E ; Takagi, Wataru ; Hyodo, Susumu ; Venkatesh, Byrappa ; Baker, Michael E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-102ccb1cd4182404a03256b793642a9ea79f8aefe7d784e72fb33fc56a24e5ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aldosterone</topic><topic>Amphibians</topic><topic>Androgens</topic><topic>Aquatic reptiles</topic><topic>Brain</topic><topic>Corticoids</topic><topic>Corticosteroids</topic><topic>Corticosterone</topic><topic>Cortisol</topic><topic>Estrogens</topic><topic>Fish</topic><topic>Glucocorticoids</topic><topic>Homeostasis</topic><topic>Hormones</topic><topic>Mineralocorticoid receptors</topic><topic>Ovaries</topic><topic>Physiological effects</topic><topic>Physiology</topic><topic>Progesterone</topic><topic>Receptors</topic><topic>Sharks</topic><topic>Steroid hormones</topic><topic>Steroids</topic><topic>Terrestrial environments</topic><topic>Transcription activation</topic><topic>Transcription factors</topic><topic>Vertebrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Katsu, Yoshinao</creatorcontrib><creatorcontrib>Kohno, Satomi</creatorcontrib><creatorcontrib>Oka, Kaori</creatorcontrib><creatorcontrib>Lin, Xiaozhi</creatorcontrib><creatorcontrib>Otake, Sumika</creatorcontrib><creatorcontrib>Pillai, Nisha E</creatorcontrib><creatorcontrib>Takagi, Wataru</creatorcontrib><creatorcontrib>Hyodo, Susumu</creatorcontrib><creatorcontrib>Venkatesh, Byrappa</creatorcontrib><creatorcontrib>Baker, Michael E</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Science signaling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Katsu, Yoshinao</au><au>Kohno, Satomi</au><au>Oka, Kaori</au><au>Lin, Xiaozhi</au><au>Otake, Sumika</au><au>Pillai, Nisha E</au><au>Takagi, Wataru</au><au>Hyodo, Susumu</au><au>Venkatesh, Byrappa</au><au>Baker, Michael E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptional activation of elephant shark mineralocorticoid receptor by corticosteroids, progesterone, and spironolactone</atitle><jtitle>Science signaling</jtitle><addtitle>Sci Signal</addtitle><date>2019-06-04</date><risdate>2019</risdate><volume>12</volume><issue>584</issue><issn>1945-0877</issn><eissn>1937-9145</eissn><abstract>The mineralocorticoid receptor (MR) is a nuclear receptor and part of a large and diverse family of transcription factors that also includes receptors for glucocorticoids, progesterone, androgens, and estrogens. The corticosteroid aldosterone is the physiological activator of the MR in humans and other terrestrial vertebrates; however, its activator is not known in cartilaginous fish, the oldest group of extant jawed vertebrates. Here, we analyzed the ability of corticosteroids and progesterone to activate the full-length MR from the elephant shark (
). On the basis of their measured activities, aldosterone, cortisol, 11-deoxycorticosterone, corticosterone, 11-deoxcortisol, progesterone, and 19-norprogesterone are potential physiological mineralocorticoids. However, aldosterone, the physiological mineralocorticoid in humans and other terrestrial vertebrates, is not found in cartilaginous or ray-finned fish. Although progesterone activates MRs in ray-finned fish, progesterone does not activate MRs in humans, amphibians, or alligator, suggesting that during the transition to terrestrial vertebrates, progesterone lost the ability to activate the MR. Both elephant shark MR and human MR are expressed in the brain, heart, ovary, testis, and other nonepithelial tissues, suggesting that MR expression in diverse tissues evolved in the common ancestor of jawed vertebrates. Our data suggest that 19-norprogesterone- and progesterone-activated MR may have unappreciated functions in reproductive physiology.</abstract><cop>United States</cop><pub>The American Association for the Advancement of Science</pub><pmid>31164478</pmid><doi>10.1126/scisignal.aar2668</doi><orcidid>https://orcid.org/0000-0001-6184-3616</orcidid><orcidid>https://orcid.org/0000-0002-8084-8145</orcidid><orcidid>https://orcid.org/0000-0003-4387-3269</orcidid><orcidid>https://orcid.org/0000-0003-2625-4626</orcidid><orcidid>https://orcid.org/0000-0002-7882-0223</orcidid><orcidid>https://orcid.org/0000-0003-2024-6721</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aldosterone Amphibians Androgens Aquatic reptiles Brain Corticoids Corticosteroids Corticosterone Cortisol Estrogens Fish Glucocorticoids Homeostasis Hormones Mineralocorticoid receptors Ovaries Physiological effects Physiology Progesterone Receptors Sharks Steroid hormones Steroids Terrestrial environments Transcription activation Transcription factors Vertebrates |
title | Transcriptional activation of elephant shark mineralocorticoid receptor by corticosteroids, progesterone, and spironolactone |
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