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A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts
Reef-building corals maintain an intracellular photosymbiotic association with dinoflagellate algae. As the algae are hosted inside the symbiosome, all metabolic exchanges must take place across the symbiosome membrane. Using functional studies in Xenopus oocytes, immunolocalization, and confocal Ai...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916725/ https://www.ncbi.nlm.nih.gov/pubmed/35275725 http://dx.doi.org/10.1126/sciadv.abm0303 |
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author | Thies, Angus B. Quijada-Rodriguez, Alex R. Zhouyao, Haonan Weihrauch, Dirk Tresguerres, Martin |
author_facet | Thies, Angus B. Quijada-Rodriguez, Alex R. Zhouyao, Haonan Weihrauch, Dirk Tresguerres, Martin |
author_sort | Thies, Angus B. |
collection | PubMed |
description | Reef-building corals maintain an intracellular photosymbiotic association with dinoflagellate algae. As the algae are hosted inside the symbiosome, all metabolic exchanges must take place across the symbiosome membrane. Using functional studies in Xenopus oocytes, immunolocalization, and confocal Airyscan microscopy, we established that Acropora yongei Rh (ayRhp1) facilitates transmembrane NH(3) and CO(2) diffusion and that it is present in the symbiosome membrane. Furthermore, ayRhp1 abundance in the symbiosome membrane was highest around midday and lowest around midnight. We conclude that ayRhp1 mediates a symbiosomal NH(4)(+)-trapping mechanism that promotes nitrogen delivery to algae during the day—necessary to sustain photosynthesis—and restricts nitrogen delivery at night—to keep algae under nitrogen limitation. The role of ayRhp1-facilitated CO(2) diffusion is less clear, but it may have implications for metabolic dysregulation between symbiotic partners and bleaching. This previously unknown mechanism expands our understanding of symbioses at the immediate animal-microbe interface, the symbiosome. |
format | Online Article Text |
id | pubmed-8916725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-89167252022-03-21 A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts Thies, Angus B. Quijada-Rodriguez, Alex R. Zhouyao, Haonan Weihrauch, Dirk Tresguerres, Martin Sci Adv Earth, Environmental, Ecological, and Space Sciences Reef-building corals maintain an intracellular photosymbiotic association with dinoflagellate algae. As the algae are hosted inside the symbiosome, all metabolic exchanges must take place across the symbiosome membrane. Using functional studies in Xenopus oocytes, immunolocalization, and confocal Airyscan microscopy, we established that Acropora yongei Rh (ayRhp1) facilitates transmembrane NH(3) and CO(2) diffusion and that it is present in the symbiosome membrane. Furthermore, ayRhp1 abundance in the symbiosome membrane was highest around midday and lowest around midnight. We conclude that ayRhp1 mediates a symbiosomal NH(4)(+)-trapping mechanism that promotes nitrogen delivery to algae during the day—necessary to sustain photosynthesis—and restricts nitrogen delivery at night—to keep algae under nitrogen limitation. The role of ayRhp1-facilitated CO(2) diffusion is less clear, but it may have implications for metabolic dysregulation between symbiotic partners and bleaching. This previously unknown mechanism expands our understanding of symbioses at the immediate animal-microbe interface, the symbiosome. American Association for the Advancement of Science 2022-03-11 /pmc/articles/PMC8916725/ /pubmed/35275725 http://dx.doi.org/10.1126/sciadv.abm0303 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Earth, Environmental, Ecological, and Space Sciences Thies, Angus B. Quijada-Rodriguez, Alex R. Zhouyao, Haonan Weihrauch, Dirk Tresguerres, Martin A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts |
title | A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts |
title_full | A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts |
title_fullStr | A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts |
title_full_unstemmed | A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts |
title_short | A Rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate NH(3) and CO(2) delivery to algal symbionts |
title_sort | rhesus channel in the coral symbiosome membrane suggests a novel mechanism to regulate nh(3) and co(2) delivery to algal symbionts |
topic | Earth, Environmental, Ecological, and Space Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8916725/ https://www.ncbi.nlm.nih.gov/pubmed/35275725 http://dx.doi.org/10.1126/sciadv.abm0303 |
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