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The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation
To study the critical role of mineralocorticoid signalling, we generated a constitutive mineralocorticoid receptor (MR)-knockout (KO) medaka as the first adult-viable MR-KO animal. This KO medaka displayed abnormal behaviours affected by visual stimuli. In contrast, the loss of MR did not result in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726310/ https://www.ncbi.nlm.nih.gov/pubmed/29231924 http://dx.doi.org/10.1038/sdata.2017.189 |
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author | Sakamoto, Tatsuya Yoshiki, Madoka Sakamoto, Hirotaka |
author_facet | Sakamoto, Tatsuya Yoshiki, Madoka Sakamoto, Hirotaka |
author_sort | Sakamoto, Tatsuya |
collection | PubMed |
description | To study the critical role of mineralocorticoid signalling, we generated a constitutive mineralocorticoid receptor (MR)-knockout (KO) medaka as the first adult-viable MR-KO animal. This KO medaka displayed abnormal behaviours affected by visual stimuli. In contrast, the loss of MR did not result in overt phenotypic changes in osmoregulation, despite the well-known osmoregulatory functions of MR in mammals. Since glucocorticoid receptor (GR) has been suggested to compensate for loss of MR, we examined expression of duplicated GRs with markedly different ligand sensitivities, in various tissues. qRT-PCR results revealed that the absence of MR induced GR1 in the brain and eyes, but not in osmoregulatory organs. This reinforces the important functions of glucocorticoid signalling, but the minor role of mineralocorticoid signalling, in fish osmoregulation. Because both 11-deoxycorticosterone (DOC) and cortisol are ligands for MR, whereas GRs are specific to cortisol, GR1 signalling may compensate for the absence of cortisol-MR, rather than that of DOC-MR. Thus, this GR expression suggests that our MR-KO model can be used specifically to characterize DOC-MR signalling. |
format | Online Article Text |
id | pubmed-5726310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57263102017-12-14 The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation Sakamoto, Tatsuya Yoshiki, Madoka Sakamoto, Hirotaka Sci Data Data Descriptor To study the critical role of mineralocorticoid signalling, we generated a constitutive mineralocorticoid receptor (MR)-knockout (KO) medaka as the first adult-viable MR-KO animal. This KO medaka displayed abnormal behaviours affected by visual stimuli. In contrast, the loss of MR did not result in overt phenotypic changes in osmoregulation, despite the well-known osmoregulatory functions of MR in mammals. Since glucocorticoid receptor (GR) has been suggested to compensate for loss of MR, we examined expression of duplicated GRs with markedly different ligand sensitivities, in various tissues. qRT-PCR results revealed that the absence of MR induced GR1 in the brain and eyes, but not in osmoregulatory organs. This reinforces the important functions of glucocorticoid signalling, but the minor role of mineralocorticoid signalling, in fish osmoregulation. Because both 11-deoxycorticosterone (DOC) and cortisol are ligands for MR, whereas GRs are specific to cortisol, GR1 signalling may compensate for the absence of cortisol-MR, rather than that of DOC-MR. Thus, this GR expression suggests that our MR-KO model can be used specifically to characterize DOC-MR signalling. Nature Publishing Group 2017-12-12 /pmc/articles/PMC5726310/ /pubmed/29231924 http://dx.doi.org/10.1038/sdata.2017.189 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ The Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ applies to the metadata files made available in this article. |
spellingShingle | Data Descriptor Sakamoto, Tatsuya Yoshiki, Madoka Sakamoto, Hirotaka The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation |
title | The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation |
title_full | The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation |
title_fullStr | The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation |
title_full_unstemmed | The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation |
title_short | The mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation |
title_sort | mineralocorticoid receptor knockout in medaka is further validated by glucocorticoid receptor compensation |
topic | Data Descriptor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726310/ https://www.ncbi.nlm.nih.gov/pubmed/29231924 http://dx.doi.org/10.1038/sdata.2017.189 |
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