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Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids
Plastids surrounded by four membranes harbor a special compartment between the outer and inner plastid membrane pair, the so-called periplastidal compartment (PPC). This cellular structure is usually presumed to be the reduced cytoplasm of a eukaryotic phototrophic endosymbiont, which was integrated...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105332/ https://www.ncbi.nlm.nih.gov/pubmed/30085124 http://dx.doi.org/10.1093/gbe/evy156 |
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author | Grosche, Christopher Diehl, Angelika Rensing, Stefan A Maier, Uwe G |
author_facet | Grosche, Christopher Diehl, Angelika Rensing, Stefan A Maier, Uwe G |
author_sort | Grosche, Christopher |
collection | PubMed |
description | Plastids surrounded by four membranes harbor a special compartment between the outer and inner plastid membrane pair, the so-called periplastidal compartment (PPC). This cellular structure is usually presumed to be the reduced cytoplasm of a eukaryotic phototrophic endosymbiont, which was integrated into a host cell and streamlined into a plastid with a complex membrane structure. Up to date, no mitochondrion or mitochondrion-related organelle has been identified in the PPC of any representative. However, two prominent groups, the cryptophytes and the chlorarachniophytes, still harbor a reduced cell nucleus of symbiont origin, the nucleomorph, in their PPCs. Generally, many cytoplasmic and nucleus-located eukaryotic proteins need an iron–sulfur cofactor for their functionality. Beside some exceptions, their synthesis is depending on a so-called iron–sulfur complex (ISC) assembly machinery located in the mitochondrion. This machinery provides the cytoplasm with a still unknown sulfur component, which is then converted into iron–sulfur clusters via a cytosolic iron–sulfur protein assembly (CIA) machinery. Here, we investigated if a CIA machinery is present in mitochondrion-lacking PPCs. By using bioinformatic screens and in vivo-localizations of candidate proteins, we show that the presence of a PPC-specific CIA machinery correlates with the presence of a nucleomorph. Phylogenetic analyses of PPC- and host specific CIA components additionally indicate a complex evolution of the CIA machineries in organisms having plastids surrounded by four membranes. |
format | Online Article Text |
id | pubmed-6105332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61053322018-08-27 Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids Grosche, Christopher Diehl, Angelika Rensing, Stefan A Maier, Uwe G Genome Biol Evol Research Article Plastids surrounded by four membranes harbor a special compartment between the outer and inner plastid membrane pair, the so-called periplastidal compartment (PPC). This cellular structure is usually presumed to be the reduced cytoplasm of a eukaryotic phototrophic endosymbiont, which was integrated into a host cell and streamlined into a plastid with a complex membrane structure. Up to date, no mitochondrion or mitochondrion-related organelle has been identified in the PPC of any representative. However, two prominent groups, the cryptophytes and the chlorarachniophytes, still harbor a reduced cell nucleus of symbiont origin, the nucleomorph, in their PPCs. Generally, many cytoplasmic and nucleus-located eukaryotic proteins need an iron–sulfur cofactor for their functionality. Beside some exceptions, their synthesis is depending on a so-called iron–sulfur complex (ISC) assembly machinery located in the mitochondrion. This machinery provides the cytoplasm with a still unknown sulfur component, which is then converted into iron–sulfur clusters via a cytosolic iron–sulfur protein assembly (CIA) machinery. Here, we investigated if a CIA machinery is present in mitochondrion-lacking PPCs. By using bioinformatic screens and in vivo-localizations of candidate proteins, we show that the presence of a PPC-specific CIA machinery correlates with the presence of a nucleomorph. Phylogenetic analyses of PPC- and host specific CIA components additionally indicate a complex evolution of the CIA machineries in organisms having plastids surrounded by four membranes. Oxford University Press 2018-08-02 /pmc/articles/PMC6105332/ /pubmed/30085124 http://dx.doi.org/10.1093/gbe/evy156 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Grosche, Christopher Diehl, Angelika Rensing, Stefan A Maier, Uwe G Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids |
title | Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids |
title_full | Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids |
title_fullStr | Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids |
title_full_unstemmed | Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids |
title_short | Iron–Sulfur Cluster Biosynthesis in Algae with Complex Plastids |
title_sort | iron–sulfur cluster biosynthesis in algae with complex plastids |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105332/ https://www.ncbi.nlm.nih.gov/pubmed/30085124 http://dx.doi.org/10.1093/gbe/evy156 |
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