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Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis
Many multicellular organisms rely on symbiotic associations for support of metabolic activity, protection, or energy. Understanding the mechanisms involved in controlling such interactions remains a major challenge. In an unbiased approach we identified key players that control the symbiosis between...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019070/ https://www.ncbi.nlm.nih.gov/pubmed/29848439 http://dx.doi.org/10.7554/eLife.35122 |
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author | Hamada, Mayuko Schröder, Katja Bathia, Jay Kürn, Ulrich Fraune, Sebastian Khalturina, Mariia Khalturin, Konstantin Shinzato, Chuya Satoh, Nori Bosch, Thomas CG |
author_facet | Hamada, Mayuko Schröder, Katja Bathia, Jay Kürn, Ulrich Fraune, Sebastian Khalturina, Mariia Khalturin, Konstantin Shinzato, Chuya Satoh, Nori Bosch, Thomas CG |
author_sort | Hamada, Mayuko |
collection | PubMed |
description | Many multicellular organisms rely on symbiotic associations for support of metabolic activity, protection, or energy. Understanding the mechanisms involved in controlling such interactions remains a major challenge. In an unbiased approach we identified key players that control the symbiosis between Hydra viridissima and its photosynthetic symbiont Chlorella sp. A99. We discovered significant up-regulation of Hydra genes encoding a phosphate transporter and glutamine synthetase suggesting regulated nutrition supply between host and symbionts. Interestingly, supplementing the medium with glutamine temporarily supports in vitro growth of the otherwise obligate symbiotic Chlorella, indicating loss of autonomy and dependence on the host. Genome sequencing of Chlorella sp. A99 revealed a large number of amino acid transporters and a degenerated nitrate assimilation pathway, presumably as consequence of the adaptation to the host environment. Our observations portray ancient symbiotic interactions as a codependent partnership in which exchange of nutrients appears to be the primary driving force. |
format | Online Article Text |
id | pubmed-6019070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60190702018-07-05 Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis Hamada, Mayuko Schröder, Katja Bathia, Jay Kürn, Ulrich Fraune, Sebastian Khalturina, Mariia Khalturin, Konstantin Shinzato, Chuya Satoh, Nori Bosch, Thomas CG eLife Evolutionary Biology Many multicellular organisms rely on symbiotic associations for support of metabolic activity, protection, or energy. Understanding the mechanisms involved in controlling such interactions remains a major challenge. In an unbiased approach we identified key players that control the symbiosis between Hydra viridissima and its photosynthetic symbiont Chlorella sp. A99. We discovered significant up-regulation of Hydra genes encoding a phosphate transporter and glutamine synthetase suggesting regulated nutrition supply between host and symbionts. Interestingly, supplementing the medium with glutamine temporarily supports in vitro growth of the otherwise obligate symbiotic Chlorella, indicating loss of autonomy and dependence on the host. Genome sequencing of Chlorella sp. A99 revealed a large number of amino acid transporters and a degenerated nitrate assimilation pathway, presumably as consequence of the adaptation to the host environment. Our observations portray ancient symbiotic interactions as a codependent partnership in which exchange of nutrients appears to be the primary driving force. eLife Sciences Publications, Ltd 2018-05-31 /pmc/articles/PMC6019070/ /pubmed/29848439 http://dx.doi.org/10.7554/eLife.35122 Text en © 2018, Hamada et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Evolutionary Biology Hamada, Mayuko Schröder, Katja Bathia, Jay Kürn, Ulrich Fraune, Sebastian Khalturina, Mariia Khalturin, Konstantin Shinzato, Chuya Satoh, Nori Bosch, Thomas CG Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis |
title | Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis |
title_full | Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis |
title_fullStr | Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis |
title_full_unstemmed | Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis |
title_short | Metabolic co-dependence drives the evolutionarily ancient Hydra–Chlorella symbiosis |
title_sort | metabolic co-dependence drives the evolutionarily ancient hydra–chlorella symbiosis |
topic | Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6019070/ https://www.ncbi.nlm.nih.gov/pubmed/29848439 http://dx.doi.org/10.7554/eLife.35122 |
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