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A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids

BACKGROUND: Light, the driving force of photosynthesis, can be harmful when present in excess; therefore, any light harvesting system requires photoprotection. Members of the extended light-harvesting complex (LHC) protein superfamily are involved in light harvesting as well as in photoprotection an...

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Autores principales: Sturm, Sabine, Engelken, Johannes, Gruber, Ansgar, Vugrinec, Sascha, G Kroth, Peter, Adamska, Iwona, Lavaud, Johann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750529/
https://www.ncbi.nlm.nih.gov/pubmed/23899289
http://dx.doi.org/10.1186/1471-2148-13-159
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author Sturm, Sabine
Engelken, Johannes
Gruber, Ansgar
Vugrinec, Sascha
G Kroth, Peter
Adamska, Iwona
Lavaud, Johann
author_facet Sturm, Sabine
Engelken, Johannes
Gruber, Ansgar
Vugrinec, Sascha
G Kroth, Peter
Adamska, Iwona
Lavaud, Johann
author_sort Sturm, Sabine
collection PubMed
description BACKGROUND: Light, the driving force of photosynthesis, can be harmful when present in excess; therefore, any light harvesting system requires photoprotection. Members of the extended light-harvesting complex (LHC) protein superfamily are involved in light harvesting as well as in photoprotection and are found in the red and green plant lineages, with a complex distribution pattern of subfamilies in the different algal lineages. RESULTS: Here, we demonstrate that the recently discovered “red lineage chlorophyll a/b-binding-like proteins” (RedCAPs) form a monophyletic family within this protein superfamily. The occurrence of RedCAPs was found to be restricted to the red algal lineage, including red algae (with primary plastids) as well as cryptophytes, haptophytes and heterokontophytes (with secondary plastids of red algal origin). Expression of a full-length RedCAP:GFP fusion construct in the diatom Phaeodactylum tricornutum confirmed the predicted plastid localisation of RedCAPs. Furthermore, we observed that similarly to the fucoxanthin chlorophyll a/c-binding light-harvesting antenna proteins also RedCAP transcripts in diatoms were regulated in a diurnal way at standard light conditions and strongly repressed at high light intensities. CONCLUSIONS: The absence of RedCAPs from the green lineage implies that RedCAPs evolved in the red lineage after separation from the the green lineage. During the evolution of secondary plastids, RedCAP genes therefore must have been transferred from the nucleus of the endocytobiotic alga to the nucleus of the host cell, a process that involved complementation with pre-sequences allowing import of the gene product into the secondary plastid bound by four membranes. Based on light-dependent transcription and on localisation data, we propose that RedCAPs might participate in the light (intensity and quality)-dependent structural or functional reorganisation of the light-harvesting antennae of the photosystems upon dark to light shifts as regularly experienced by diatoms in nature. Remarkably, in plastids of the red lineage as well as in green lineage plastids, the phycobilisome based cyanobacterial light harvesting system has been replaced by light harvesting systems that are based on members of the extended LHC protein superfamily, either for one of the photosystems (PS I of red algae) or for both (diatoms). In their proposed function, the RedCAP protein family may thus have played a role in the evolutionary structural remodelling of light-harvesting antennae in the red lineage.
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spelling pubmed-37505292013-08-24 A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids Sturm, Sabine Engelken, Johannes Gruber, Ansgar Vugrinec, Sascha G Kroth, Peter Adamska, Iwona Lavaud, Johann BMC Evol Biol Research Article BACKGROUND: Light, the driving force of photosynthesis, can be harmful when present in excess; therefore, any light harvesting system requires photoprotection. Members of the extended light-harvesting complex (LHC) protein superfamily are involved in light harvesting as well as in photoprotection and are found in the red and green plant lineages, with a complex distribution pattern of subfamilies in the different algal lineages. RESULTS: Here, we demonstrate that the recently discovered “red lineage chlorophyll a/b-binding-like proteins” (RedCAPs) form a monophyletic family within this protein superfamily. The occurrence of RedCAPs was found to be restricted to the red algal lineage, including red algae (with primary plastids) as well as cryptophytes, haptophytes and heterokontophytes (with secondary plastids of red algal origin). Expression of a full-length RedCAP:GFP fusion construct in the diatom Phaeodactylum tricornutum confirmed the predicted plastid localisation of RedCAPs. Furthermore, we observed that similarly to the fucoxanthin chlorophyll a/c-binding light-harvesting antenna proteins also RedCAP transcripts in diatoms were regulated in a diurnal way at standard light conditions and strongly repressed at high light intensities. CONCLUSIONS: The absence of RedCAPs from the green lineage implies that RedCAPs evolved in the red lineage after separation from the the green lineage. During the evolution of secondary plastids, RedCAP genes therefore must have been transferred from the nucleus of the endocytobiotic alga to the nucleus of the host cell, a process that involved complementation with pre-sequences allowing import of the gene product into the secondary plastid bound by four membranes. Based on light-dependent transcription and on localisation data, we propose that RedCAPs might participate in the light (intensity and quality)-dependent structural or functional reorganisation of the light-harvesting antennae of the photosystems upon dark to light shifts as regularly experienced by diatoms in nature. Remarkably, in plastids of the red lineage as well as in green lineage plastids, the phycobilisome based cyanobacterial light harvesting system has been replaced by light harvesting systems that are based on members of the extended LHC protein superfamily, either for one of the photosystems (PS I of red algae) or for both (diatoms). In their proposed function, the RedCAP protein family may thus have played a role in the evolutionary structural remodelling of light-harvesting antennae in the red lineage. BioMed Central 2013-07-30 /pmc/articles/PMC3750529/ /pubmed/23899289 http://dx.doi.org/10.1186/1471-2148-13-159 Text en Copyright © 2013 Sturm et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sturm, Sabine
Engelken, Johannes
Gruber, Ansgar
Vugrinec, Sascha
G Kroth, Peter
Adamska, Iwona
Lavaud, Johann
A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids
title A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids
title_full A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids
title_fullStr A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids
title_full_unstemmed A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids
title_short A novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids
title_sort novel type of light-harvesting antenna protein of red algal origin in algae with secondary plastids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750529/
https://www.ncbi.nlm.nih.gov/pubmed/23899289
http://dx.doi.org/10.1186/1471-2148-13-159
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