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Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs

The kleptoplastic sea slug Elysia chlorotica consumes Vaucheria litorea, stealing its plastids, which then photosynthesize inside the animal cells for months. We investigated the properties of V. litorea plastids to understand how they withstand the rigors of photosynthesis in isolation. Transcripti...

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Autores principales: Havurinne, Vesa, Handrich, Maria, Antinluoma, Mikko, Khorobrykh, Sergey, Gould, Sven B, Tyystjärvi, Esa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318255/
https://www.ncbi.nlm.nih.gov/pubmed/33989402
http://dx.doi.org/10.1093/jxb/erab216
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author Havurinne, Vesa
Handrich, Maria
Antinluoma, Mikko
Khorobrykh, Sergey
Gould, Sven B
Tyystjärvi, Esa
author_facet Havurinne, Vesa
Handrich, Maria
Antinluoma, Mikko
Khorobrykh, Sergey
Gould, Sven B
Tyystjärvi, Esa
author_sort Havurinne, Vesa
collection PubMed
description The kleptoplastic sea slug Elysia chlorotica consumes Vaucheria litorea, stealing its plastids, which then photosynthesize inside the animal cells for months. We investigated the properties of V. litorea plastids to understand how they withstand the rigors of photosynthesis in isolation. Transcription of specific genes in laboratory-isolated V. litorea plastids was monitored for 7 days. The involvement of plastid-encoded FtsH, a key plastid maintenance protease, in recovery from photoinhibition in V. litorea was estimated in cycloheximide-treated cells. In vitro comparison of V. litorea and spinach thylakoids was applied to investigate reactive oxygen species formation in V. litorea. In comparison to other tested genes, the transcripts of ftsH and translation elongation factor EF-Tu (tufA) decreased slowly in isolated V. litorea plastids. Higher levels of FtsH were also evident in cycloheximide-treated cells during recovery from photoinhibition. Charge recombination in PSII of V. litorea was found to be fine-tuned to produce only small quantities of singlet oxygen, and the plastids also contained reactive oxygen species-protective compounds. Our results support the view that the genetic characteristics of the plastids are crucial in creating a photosynthetic sea slug. The plastid’s autonomous repair machinery is likely enhanced by low singlet oxygen production and elevated expression of FtsH.
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spelling pubmed-83182552021-07-29 Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs Havurinne, Vesa Handrich, Maria Antinluoma, Mikko Khorobrykh, Sergey Gould, Sven B Tyystjärvi, Esa J Exp Bot Research Papers The kleptoplastic sea slug Elysia chlorotica consumes Vaucheria litorea, stealing its plastids, which then photosynthesize inside the animal cells for months. We investigated the properties of V. litorea plastids to understand how they withstand the rigors of photosynthesis in isolation. Transcription of specific genes in laboratory-isolated V. litorea plastids was monitored for 7 days. The involvement of plastid-encoded FtsH, a key plastid maintenance protease, in recovery from photoinhibition in V. litorea was estimated in cycloheximide-treated cells. In vitro comparison of V. litorea and spinach thylakoids was applied to investigate reactive oxygen species formation in V. litorea. In comparison to other tested genes, the transcripts of ftsH and translation elongation factor EF-Tu (tufA) decreased slowly in isolated V. litorea plastids. Higher levels of FtsH were also evident in cycloheximide-treated cells during recovery from photoinhibition. Charge recombination in PSII of V. litorea was found to be fine-tuned to produce only small quantities of singlet oxygen, and the plastids also contained reactive oxygen species-protective compounds. Our results support the view that the genetic characteristics of the plastids are crucial in creating a photosynthetic sea slug. The plastid’s autonomous repair machinery is likely enhanced by low singlet oxygen production and elevated expression of FtsH. Oxford University Press 2021-05-15 /pmc/articles/PMC8318255/ /pubmed/33989402 http://dx.doi.org/10.1093/jxb/erab216 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Experimental Biology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Havurinne, Vesa
Handrich, Maria
Antinluoma, Mikko
Khorobrykh, Sergey
Gould, Sven B
Tyystjärvi, Esa
Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs
title Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs
title_full Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs
title_fullStr Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs
title_full_unstemmed Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs
title_short Genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs
title_sort genetic autonomy and low singlet oxygen yield support kleptoplast functionality in photosynthetic sea slugs
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318255/
https://www.ncbi.nlm.nih.gov/pubmed/33989402
http://dx.doi.org/10.1093/jxb/erab216
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