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Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka
In mammals the melanocortin 4 receptor (Mc4r) signaling system has been mainly associated with the regulation of appetite and energy homeostasis. In fish of the genus Xiphophorus (platyfish and swordtails) puberty onset is genetically determined by a single locus, which encodes the mc4r. Wild popula...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463759/ https://www.ncbi.nlm.nih.gov/pubmed/31024451 http://dx.doi.org/10.3389/fendo.2019.00213 |
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author | Liu, Ruiqi Kinoshita, Masato Adolfi, Mateus C. Schartl, Manfred |
author_facet | Liu, Ruiqi Kinoshita, Masato Adolfi, Mateus C. Schartl, Manfred |
author_sort | Liu, Ruiqi |
collection | PubMed |
description | In mammals the melanocortin 4 receptor (Mc4r) signaling system has been mainly associated with the regulation of appetite and energy homeostasis. In fish of the genus Xiphophorus (platyfish and swordtails) puberty onset is genetically determined by a single locus, which encodes the mc4r. Wild populations of Xiphophorus are polymorphic for early and late-maturing individuals. Copy number variation of different mc4r alleles is responsible for the difference in puberty onset. To answer whether this is a special adaptation of the Mc4r signaling system in the lineage of Xiphophorus or a more widely conserved mechanism in teleosts, we studied the role of Mc4r in reproductive biology of medaka (Oryzias latipes), a close relative to Xiphophorus and a well-established model to study gonadal development. To understand the potential role of Mc4r in medaka, we characterized the major features of the Mc4r signaling system (mc4r, mrap2, pomc, agrp1). In medaka, all these genes are expressed before hatching. In adults, they are mainly expressed in the brain. The transcript of the receptor accessory protein mrap2 co-localizes with mc4r in the hypothalamus in adult brains indicating a conserved function of modulating Mc4r signaling. Comparing growth and puberty between wild-type and mc4r knockout medaka revealed that absence of Mc4r does not change puberty timing but significantly delays hatching. Embryonic development of knockout animals is retarded compared to wild-types. In conclusion, the Mc4r system in medaka is involved in regulation of growth rather than puberty. |
format | Online Article Text |
id | pubmed-6463759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64637592019-04-25 Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka Liu, Ruiqi Kinoshita, Masato Adolfi, Mateus C. Schartl, Manfred Front Endocrinol (Lausanne) Endocrinology In mammals the melanocortin 4 receptor (Mc4r) signaling system has been mainly associated with the regulation of appetite and energy homeostasis. In fish of the genus Xiphophorus (platyfish and swordtails) puberty onset is genetically determined by a single locus, which encodes the mc4r. Wild populations of Xiphophorus are polymorphic for early and late-maturing individuals. Copy number variation of different mc4r alleles is responsible for the difference in puberty onset. To answer whether this is a special adaptation of the Mc4r signaling system in the lineage of Xiphophorus or a more widely conserved mechanism in teleosts, we studied the role of Mc4r in reproductive biology of medaka (Oryzias latipes), a close relative to Xiphophorus and a well-established model to study gonadal development. To understand the potential role of Mc4r in medaka, we characterized the major features of the Mc4r signaling system (mc4r, mrap2, pomc, agrp1). In medaka, all these genes are expressed before hatching. In adults, they are mainly expressed in the brain. The transcript of the receptor accessory protein mrap2 co-localizes with mc4r in the hypothalamus in adult brains indicating a conserved function of modulating Mc4r signaling. Comparing growth and puberty between wild-type and mc4r knockout medaka revealed that absence of Mc4r does not change puberty timing but significantly delays hatching. Embryonic development of knockout animals is retarded compared to wild-types. In conclusion, the Mc4r system in medaka is involved in regulation of growth rather than puberty. Frontiers Media S.A. 2019-04-05 /pmc/articles/PMC6463759/ /pubmed/31024451 http://dx.doi.org/10.3389/fendo.2019.00213 Text en Copyright © 2019 Liu, Kinoshita, Adolfi and Schartl. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Liu, Ruiqi Kinoshita, Masato Adolfi, Mateus C. Schartl, Manfred Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka |
title | Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka |
title_full | Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka |
title_fullStr | Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka |
title_full_unstemmed | Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka |
title_short | Analysis of the Role of the Mc4r System in Development, Growth, and Puberty of Medaka |
title_sort | analysis of the role of the mc4r system in development, growth, and puberty of medaka |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6463759/ https://www.ncbi.nlm.nih.gov/pubmed/31024451 http://dx.doi.org/10.3389/fendo.2019.00213 |
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