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Divalent metal transporter-related protein restricts animals to marine habitats

Utilization and regulation of metals from seawater by marine organisms are important physiological processes. To better understand metal regulation, we searched the crown-of-thorns starfish genome for the divalent metal transporter (DMT) gene, a membrane protein responsible for uptake of divalent ca...

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Autores principales: Sassa, Mieko, Takagi, Toshiyuki, Kinjo, Azusa, Yoshioka, Yuki, Zayasu, Yuna, Shinzato, Chuya, Kanda, Shinji, Murakami-Sugihara, Naoko, Shirai, Kotaro, Inoue, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041893/
https://www.ncbi.nlm.nih.gov/pubmed/33846549
http://dx.doi.org/10.1038/s42003-021-01984-8
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author Sassa, Mieko
Takagi, Toshiyuki
Kinjo, Azusa
Yoshioka, Yuki
Zayasu, Yuna
Shinzato, Chuya
Kanda, Shinji
Murakami-Sugihara, Naoko
Shirai, Kotaro
Inoue, Koji
author_facet Sassa, Mieko
Takagi, Toshiyuki
Kinjo, Azusa
Yoshioka, Yuki
Zayasu, Yuna
Shinzato, Chuya
Kanda, Shinji
Murakami-Sugihara, Naoko
Shirai, Kotaro
Inoue, Koji
author_sort Sassa, Mieko
collection PubMed
description Utilization and regulation of metals from seawater by marine organisms are important physiological processes. To better understand metal regulation, we searched the crown-of-thorns starfish genome for the divalent metal transporter (DMT) gene, a membrane protein responsible for uptake of divalent cations. We found two DMT-like sequences. One is an ortholog of vertebrate DMT, but the other is an unknown protein, which we named DMT-related protein (DMTRP). Functional analysis using a yeast expression system demonstrated that DMT transports various metals, like known DMTs, but DMTRP does not. In contrast, DMTRP reduced the intracellular concentration of some metals, especially zinc, suggesting its involvement in negative regulation of metal uptake. Phylogenetic distribution of the DMTRP gene in various metazoans, including sponges, protostomes, and deuterostomes, indicates that it originated early in metazoan evolution. However, the DMTRP gene is only retained in marine species, and its loss seems to have occurred independently in ecdysozoan and vertebrate lineages from which major freshwater and land animals appeared. DMTRP may be an evolutionary and ecological limitation, restricting organisms that possess it to marine habitats, whereas its loss may have allowed other organisms to invade freshwater and terrestrial habitats.
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spelling pubmed-80418932021-04-28 Divalent metal transporter-related protein restricts animals to marine habitats Sassa, Mieko Takagi, Toshiyuki Kinjo, Azusa Yoshioka, Yuki Zayasu, Yuna Shinzato, Chuya Kanda, Shinji Murakami-Sugihara, Naoko Shirai, Kotaro Inoue, Koji Commun Biol Article Utilization and regulation of metals from seawater by marine organisms are important physiological processes. To better understand metal regulation, we searched the crown-of-thorns starfish genome for the divalent metal transporter (DMT) gene, a membrane protein responsible for uptake of divalent cations. We found two DMT-like sequences. One is an ortholog of vertebrate DMT, but the other is an unknown protein, which we named DMT-related protein (DMTRP). Functional analysis using a yeast expression system demonstrated that DMT transports various metals, like known DMTs, but DMTRP does not. In contrast, DMTRP reduced the intracellular concentration of some metals, especially zinc, suggesting its involvement in negative regulation of metal uptake. Phylogenetic distribution of the DMTRP gene in various metazoans, including sponges, protostomes, and deuterostomes, indicates that it originated early in metazoan evolution. However, the DMTRP gene is only retained in marine species, and its loss seems to have occurred independently in ecdysozoan and vertebrate lineages from which major freshwater and land animals appeared. DMTRP may be an evolutionary and ecological limitation, restricting organisms that possess it to marine habitats, whereas its loss may have allowed other organisms to invade freshwater and terrestrial habitats. Nature Publishing Group UK 2021-04-12 /pmc/articles/PMC8041893/ /pubmed/33846549 http://dx.doi.org/10.1038/s42003-021-01984-8 Text en © The Author(s) 2021 https://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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sassa, Mieko
Takagi, Toshiyuki
Kinjo, Azusa
Yoshioka, Yuki
Zayasu, Yuna
Shinzato, Chuya
Kanda, Shinji
Murakami-Sugihara, Naoko
Shirai, Kotaro
Inoue, Koji
Divalent metal transporter-related protein restricts animals to marine habitats
title Divalent metal transporter-related protein restricts animals to marine habitats
title_full Divalent metal transporter-related protein restricts animals to marine habitats
title_fullStr Divalent metal transporter-related protein restricts animals to marine habitats
title_full_unstemmed Divalent metal transporter-related protein restricts animals to marine habitats
title_short Divalent metal transporter-related protein restricts animals to marine habitats
title_sort divalent metal transporter-related protein restricts animals to marine habitats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041893/
https://www.ncbi.nlm.nih.gov/pubmed/33846549
http://dx.doi.org/10.1038/s42003-021-01984-8
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