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Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae

Plants and algae possess plastids and mitochondria harboring their own genomes, which are replicated by the apparatus consisting of DNA polymerase, DNA primase, DNA helicase, DNA topoisomerase, single-stranded DNA maintenance protein, DNA ligase, and primer removal enzyme. In the higher plant Arabid...

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Autores principales: Moriyama, Takashi, Tajima, Naoyuki, Sekine, Kohsuke, Sato, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914683/
https://www.ncbi.nlm.nih.gov/pubmed/24407855
http://dx.doi.org/10.1093/gbe/evu009
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author Moriyama, Takashi
Tajima, Naoyuki
Sekine, Kohsuke
Sato, Naoki
author_facet Moriyama, Takashi
Tajima, Naoyuki
Sekine, Kohsuke
Sato, Naoki
author_sort Moriyama, Takashi
collection PubMed
description Plants and algae possess plastids and mitochondria harboring their own genomes, which are replicated by the apparatus consisting of DNA polymerase, DNA primase, DNA helicase, DNA topoisomerase, single-stranded DNA maintenance protein, DNA ligase, and primer removal enzyme. In the higher plant Arabidopsis thaliana, organellar replication-related enzymes (OREs) are similar in plastids and mitochondria because many of them are dually targeted to plastids and mitochondria. In the red algae, there is a report about a DNA replicase, plant/protist organellar DNA polymerase, which is localized to both plastids and mitochondria. However, other OREs remain unclear in algae. Here, we identified OREs possibly localized to organelles in the unicellular rhodophyte Cyanidioschyzon merolae. We then examined intracellular localization of green fluorescent protein-fusion proteins of these enzymes in C. merolae, whose cell has a single plastid and a single mitochondrion and is suitable for localization analysis, demonstrating that the plastid and the mitochondrion contain markedly different components of replication machinery. Phylogenetic analyses revealed that the organelle replication apparatus was composed of enzymes of various different origins, such as proteobacterial, cyanobacterial, and eukaryotic, in both red algae and green plants. Especially in the red alga, many enzymes of cyanobacterial origin remained. Finally, on the basis of the results of localization and phylogenetic analyses, we propose a model on the succession of OREs in eukaryotes.
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spelling pubmed-39146832014-02-06 Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae Moriyama, Takashi Tajima, Naoyuki Sekine, Kohsuke Sato, Naoki Genome Biol Evol Research Article Plants and algae possess plastids and mitochondria harboring their own genomes, which are replicated by the apparatus consisting of DNA polymerase, DNA primase, DNA helicase, DNA topoisomerase, single-stranded DNA maintenance protein, DNA ligase, and primer removal enzyme. In the higher plant Arabidopsis thaliana, organellar replication-related enzymes (OREs) are similar in plastids and mitochondria because many of them are dually targeted to plastids and mitochondria. In the red algae, there is a report about a DNA replicase, plant/protist organellar DNA polymerase, which is localized to both plastids and mitochondria. However, other OREs remain unclear in algae. Here, we identified OREs possibly localized to organelles in the unicellular rhodophyte Cyanidioschyzon merolae. We then examined intracellular localization of green fluorescent protein-fusion proteins of these enzymes in C. merolae, whose cell has a single plastid and a single mitochondrion and is suitable for localization analysis, demonstrating that the plastid and the mitochondrion contain markedly different components of replication machinery. Phylogenetic analyses revealed that the organelle replication apparatus was composed of enzymes of various different origins, such as proteobacterial, cyanobacterial, and eukaryotic, in both red algae and green plants. Especially in the red alga, many enzymes of cyanobacterial origin remained. Finally, on the basis of the results of localization and phylogenetic analyses, we propose a model on the succession of OREs in eukaryotes. Oxford University Press 2014-01-09 /pmc/articles/PMC3914683/ /pubmed/24407855 http://dx.doi.org/10.1093/gbe/evu009 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Moriyama, Takashi
Tajima, Naoyuki
Sekine, Kohsuke
Sato, Naoki
Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae
title Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae
title_full Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae
title_fullStr Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae
title_full_unstemmed Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae
title_short Localization and Phylogenetic Analysis of Enzymes Related to Organellar Genome Replication in the Unicellular Rhodophyte Cyanidioschyzon merolae
title_sort localization and phylogenetic analysis of enzymes related to organellar genome replication in the unicellular rhodophyte cyanidioschyzon merolae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3914683/
https://www.ncbi.nlm.nih.gov/pubmed/24407855
http://dx.doi.org/10.1093/gbe/evu009
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