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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Veröffentlicht in:Science signaling 2019-06, Vol.12 (584)
Hauptverfasser: Katsu, Yoshinao, Kohno, Satomi, Oka, Kaori, Lin, Xiaozhi, Otake, Sumika, Pillai, Nisha E, Takagi, Wataru, Hyodo, Susumu, Venkatesh, Byrappa, Baker, Michael E
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container_issue 584
container_start_page
container_title Science signaling
container_volume 12
creator Katsu, Yoshinao
Kohno, Satomi
Oka, Kaori
Lin, Xiaozhi
Otake, Sumika
Pillai, Nisha E
Takagi, Wataru
Hyodo, Susumu
Venkatesh, Byrappa
Baker, Michael E
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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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. 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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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