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Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome

Genome sequencing of Symbiodinium minutum revealed that 95 of 109 plastid-associated genes have been transferred to the nuclear genome and subsequently expanded by gene duplication. Only 14 genes remain in plastids and occur as DNA minicircles. Each minicircle (1.8–3.3 kb) contains one gene and a co...

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Autores principales: Mungpakdee, Sutada, Shinzato, Chuya, Takeuchi, Takeshi, Kawashima, Takeshi, Koyanagi, Ryo, Hisata, Kanako, Tanaka, Makiko, Goto, Hiroki, Fujie, Manabu, Lin, Senjie, Satoh, Nori, Shoguchi, Eiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079212/
https://www.ncbi.nlm.nih.gov/pubmed/24881086
http://dx.doi.org/10.1093/gbe/evu109
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author Mungpakdee, Sutada
Shinzato, Chuya
Takeuchi, Takeshi
Kawashima, Takeshi
Koyanagi, Ryo
Hisata, Kanako
Tanaka, Makiko
Goto, Hiroki
Fujie, Manabu
Lin, Senjie
Satoh, Nori
Shoguchi, Eiichi
author_facet Mungpakdee, Sutada
Shinzato, Chuya
Takeuchi, Takeshi
Kawashima, Takeshi
Koyanagi, Ryo
Hisata, Kanako
Tanaka, Makiko
Goto, Hiroki
Fujie, Manabu
Lin, Senjie
Satoh, Nori
Shoguchi, Eiichi
author_sort Mungpakdee, Sutada
collection PubMed
description Genome sequencing of Symbiodinium minutum revealed that 95 of 109 plastid-associated genes have been transferred to the nuclear genome and subsequently expanded by gene duplication. Only 14 genes remain in plastids and occur as DNA minicircles. Each minicircle (1.8–3.3 kb) contains one gene and a conserved noncoding region containing putative promoters and RNA-binding sites. Nine types of RNA editing, including a novel G/U type, were discovered in minicircle transcripts but not in genes transferred to the nucleus. In contrast to DNA editing sites in dinoflagellate mitochondria, which tend to be highly conserved across all taxa, editing sites employed in DNA minicircles are highly variable from species to species. Editing is crucial for core photosystem protein function. It restores evolutionarily conserved amino acids and increases peptidyl hydropathy. It also increases protein plasticity necessary to initiate photosystem complex assembly.
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spelling pubmed-40792122014-07-02 Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome Mungpakdee, Sutada Shinzato, Chuya Takeuchi, Takeshi Kawashima, Takeshi Koyanagi, Ryo Hisata, Kanako Tanaka, Makiko Goto, Hiroki Fujie, Manabu Lin, Senjie Satoh, Nori Shoguchi, Eiichi Genome Biol Evol Research Article Genome sequencing of Symbiodinium minutum revealed that 95 of 109 plastid-associated genes have been transferred to the nuclear genome and subsequently expanded by gene duplication. Only 14 genes remain in plastids and occur as DNA minicircles. Each minicircle (1.8–3.3 kb) contains one gene and a conserved noncoding region containing putative promoters and RNA-binding sites. Nine types of RNA editing, including a novel G/U type, were discovered in minicircle transcripts but not in genes transferred to the nucleus. In contrast to DNA editing sites in dinoflagellate mitochondria, which tend to be highly conserved across all taxa, editing sites employed in DNA minicircles are highly variable from species to species. Editing is crucial for core photosystem protein function. It restores evolutionarily conserved amino acids and increases peptidyl hydropathy. It also increases protein plasticity necessary to initiate photosystem complex assembly. Oxford University Press 2014-05-31 /pmc/articles/PMC4079212/ /pubmed/24881086 http://dx.doi.org/10.1093/gbe/evu109 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
Mungpakdee, Sutada
Shinzato, Chuya
Takeuchi, Takeshi
Kawashima, Takeshi
Koyanagi, Ryo
Hisata, Kanako
Tanaka, Makiko
Goto, Hiroki
Fujie, Manabu
Lin, Senjie
Satoh, Nori
Shoguchi, Eiichi
Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome
title Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome
title_full Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome
title_fullStr Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome
title_full_unstemmed Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome
title_short Massive Gene Transfer and Extensive RNA Editing of a Symbiotic Dinoflagellate Plastid Genome
title_sort massive gene transfer and extensive rna editing of a symbiotic dinoflagellate plastid genome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079212/
https://www.ncbi.nlm.nih.gov/pubmed/24881086
http://dx.doi.org/10.1093/gbe/evu109
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