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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...

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Autores principales: Thies, Angus B., Quijada-Rodriguez, Alex R., Zhouyao, Haonan, Weihrauch, Dirk, Tresguerres, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
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.
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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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