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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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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. |
format | Online Article Text |
id | pubmed-4079212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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