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Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor
Melatonin receptors (MTNRs) belonging to the G protein-coupled receptor family are considered to consist of three subtypes in vertebrates: MTNR1a, MTNR1b and MTNR1c. Additionally, MTNR1a-like genes have been identified in teleostean species as a fish-specific subtype of MTNR1a. However, similar mole...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602942/ https://www.ncbi.nlm.nih.gov/pubmed/31263128 http://dx.doi.org/10.1038/s41598-019-45925-2 |
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author | Sakai, Kotowa Yamamoto, Yuya Ikeuchi, Toshitaka |
author_facet | Sakai, Kotowa Yamamoto, Yuya Ikeuchi, Toshitaka |
author_sort | Sakai, Kotowa |
collection | PubMed |
description | Melatonin receptors (MTNRs) belonging to the G protein-coupled receptor family are considered to consist of three subtypes in vertebrates: MTNR1a, MTNR1b and MTNR1c. Additionally, MTNR1a-like genes have been identified in teleostean species as a fish-specific subtype of MTNR1a. However, similar molecules to this MTNR1a-like gene can be found in some reptiles upon searching the DNA database. We hypothesized that a vertebrate can essentially have four functional subtypes of MTNR as ohnologs. Thus, in the present study we examined the molecular phylogeny, expression patterns and pharmacological profile(s) using the teleost medaka (Oryzias latipes). The four conserved subtypes of MTNR (MTNR1a, MTNR1b, MTNR1c and MTNR1a-like) in vertebrates were classified based on synteny and phylogenetic analysis. The fourth MTNR, termed MTNR1a-like, could be classified as MTNR1d. It was observed by using RT-qPCR that expression patterns differed amongst these subtypes. Moreover, mtnr1a, mtnr1c and mtnr1a-like/mtnr1d expression was elevated during short days compared to long days in diencephalons. All the subtypes were activated by melatonin and transduced signals into the Gi pathway, to perform a cAMP-responsive reporter gene assay. It was shown that MTNR originally consisted of four subtypes: MTNR1a, MTNR1b, MTNR1c and MTNR1d. These subtypes were functional, at least in fish, although some organisms, including mammals, have lost one or two subtypes. |
format | Online Article Text |
id | pubmed-6602942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66029422019-07-14 Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor Sakai, Kotowa Yamamoto, Yuya Ikeuchi, Toshitaka Sci Rep Article Melatonin receptors (MTNRs) belonging to the G protein-coupled receptor family are considered to consist of three subtypes in vertebrates: MTNR1a, MTNR1b and MTNR1c. Additionally, MTNR1a-like genes have been identified in teleostean species as a fish-specific subtype of MTNR1a. However, similar molecules to this MTNR1a-like gene can be found in some reptiles upon searching the DNA database. We hypothesized that a vertebrate can essentially have four functional subtypes of MTNR as ohnologs. Thus, in the present study we examined the molecular phylogeny, expression patterns and pharmacological profile(s) using the teleost medaka (Oryzias latipes). The four conserved subtypes of MTNR (MTNR1a, MTNR1b, MTNR1c and MTNR1a-like) in vertebrates were classified based on synteny and phylogenetic analysis. The fourth MTNR, termed MTNR1a-like, could be classified as MTNR1d. It was observed by using RT-qPCR that expression patterns differed amongst these subtypes. Moreover, mtnr1a, mtnr1c and mtnr1a-like/mtnr1d expression was elevated during short days compared to long days in diencephalons. All the subtypes were activated by melatonin and transduced signals into the Gi pathway, to perform a cAMP-responsive reporter gene assay. It was shown that MTNR originally consisted of four subtypes: MTNR1a, MTNR1b, MTNR1c and MTNR1d. These subtypes were functional, at least in fish, although some organisms, including mammals, have lost one or two subtypes. Nature Publishing Group UK 2019-07-01 /pmc/articles/PMC6602942/ /pubmed/31263128 http://dx.doi.org/10.1038/s41598-019-45925-2 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Sakai, Kotowa Yamamoto, Yuya Ikeuchi, Toshitaka Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor |
title | Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor |
title_full | Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor |
title_fullStr | Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor |
title_full_unstemmed | Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor |
title_short | Vertebrates originally possess four functional subtypes of G protein-coupled melatonin receptor |
title_sort | vertebrates originally possess four functional subtypes of g protein-coupled melatonin receptor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602942/ https://www.ncbi.nlm.nih.gov/pubmed/31263128 http://dx.doi.org/10.1038/s41598-019-45925-2 |
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