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Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams

Intracellular thioautotrophic symbionts of deep-sea vesicomyid clams lack some DNA repair genes and are thought to be undergoing reductive genome evolution (RGE). In this study, we addressed two questions, 1) how these symbionts lost their DNA repair genes and 2) how such losses affect RGE. For the...

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Autores principales: Shimamura, Shigeru, Kaneko, Takashi, Ozawa, Genki, Matsumoto, Mamiko Nishino, Koshiishi, Takeru, Takaki, Yoshihiro, Kato, Chiaki, Takai, Ken, Yoshida, Takao, Fujikura, Katsunori, Barry, James P., Maruyama, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310779/
https://www.ncbi.nlm.nih.gov/pubmed/28199404
http://dx.doi.org/10.1371/journal.pone.0171274
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author Shimamura, Shigeru
Kaneko, Takashi
Ozawa, Genki
Matsumoto, Mamiko Nishino
Koshiishi, Takeru
Takaki, Yoshihiro
Kato, Chiaki
Takai, Ken
Yoshida, Takao
Fujikura, Katsunori
Barry, James P.
Maruyama, Tadashi
author_facet Shimamura, Shigeru
Kaneko, Takashi
Ozawa, Genki
Matsumoto, Mamiko Nishino
Koshiishi, Takeru
Takaki, Yoshihiro
Kato, Chiaki
Takai, Ken
Yoshida, Takao
Fujikura, Katsunori
Barry, James P.
Maruyama, Tadashi
author_sort Shimamura, Shigeru
collection PubMed
description Intracellular thioautotrophic symbionts of deep-sea vesicomyid clams lack some DNA repair genes and are thought to be undergoing reductive genome evolution (RGE). In this study, we addressed two questions, 1) how these symbionts lost their DNA repair genes and 2) how such losses affect RGE. For the first question, we examined genes associated with nucleotide excision repair (NER; uvrA, uvrB, uvrC, uvrD, uvrD paralog [uvrDp] and mfd) in 12 symbionts of vesicomyid clams belonging to two clades (5 clade I and 7 clade II symbionts). While uvrA, uvrDp and mfd were conserved in all symbionts, uvrB and uvrC were degraded in all clade I symbionts but were apparently intact in clade II symbionts. UvrD was disrupted in two clade II symbionts. Among the intact genes in Ca. Vesicomyosocius okutanii (clade I), expressions of uvrD and mfd were detected by reverse transcription-polymerase chain reaction (RT-PCR), but those of uvrA and uvrDp were not. In contrast, all intact genes were expressed in the symbiont of Calyptogena pacifica (clade II). To assess how gene losses affect RGE (question 2), genetic distances of the examined genes in symbionts from Bathymodiolus septemdierum were shown to be larger in clade I than clade II symbionts. In addition, these genes had lower guanine+cytosine (GC) content and higher repeat sequence densities in clade I than measured in clade II. Our results suggest that NER genes are currently being lost from the extant lineages of vesicomyid clam symbionts. The loss of NER genes and mutY in these symbionts is likely to promote increases in genetic distance and repeat sequence density as well as reduced GC content in genomic genes, and may have facilitated reductive evolution of the genome.
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spelling pubmed-53107792017-03-03 Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams Shimamura, Shigeru Kaneko, Takashi Ozawa, Genki Matsumoto, Mamiko Nishino Koshiishi, Takeru Takaki, Yoshihiro Kato, Chiaki Takai, Ken Yoshida, Takao Fujikura, Katsunori Barry, James P. Maruyama, Tadashi PLoS One Research Article Intracellular thioautotrophic symbionts of deep-sea vesicomyid clams lack some DNA repair genes and are thought to be undergoing reductive genome evolution (RGE). In this study, we addressed two questions, 1) how these symbionts lost their DNA repair genes and 2) how such losses affect RGE. For the first question, we examined genes associated with nucleotide excision repair (NER; uvrA, uvrB, uvrC, uvrD, uvrD paralog [uvrDp] and mfd) in 12 symbionts of vesicomyid clams belonging to two clades (5 clade I and 7 clade II symbionts). While uvrA, uvrDp and mfd were conserved in all symbionts, uvrB and uvrC were degraded in all clade I symbionts but were apparently intact in clade II symbionts. UvrD was disrupted in two clade II symbionts. Among the intact genes in Ca. Vesicomyosocius okutanii (clade I), expressions of uvrD and mfd were detected by reverse transcription-polymerase chain reaction (RT-PCR), but those of uvrA and uvrDp were not. In contrast, all intact genes were expressed in the symbiont of Calyptogena pacifica (clade II). To assess how gene losses affect RGE (question 2), genetic distances of the examined genes in symbionts from Bathymodiolus septemdierum were shown to be larger in clade I than clade II symbionts. In addition, these genes had lower guanine+cytosine (GC) content and higher repeat sequence densities in clade I than measured in clade II. Our results suggest that NER genes are currently being lost from the extant lineages of vesicomyid clam symbionts. The loss of NER genes and mutY in these symbionts is likely to promote increases in genetic distance and repeat sequence density as well as reduced GC content in genomic genes, and may have facilitated reductive evolution of the genome. Public Library of Science 2017-02-15 /pmc/articles/PMC5310779/ /pubmed/28199404 http://dx.doi.org/10.1371/journal.pone.0171274 Text en © 2017 Shimamura et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shimamura, Shigeru
Kaneko, Takashi
Ozawa, Genki
Matsumoto, Mamiko Nishino
Koshiishi, Takeru
Takaki, Yoshihiro
Kato, Chiaki
Takai, Ken
Yoshida, Takao
Fujikura, Katsunori
Barry, James P.
Maruyama, Tadashi
Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams
title Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams
title_full Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams
title_fullStr Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams
title_full_unstemmed Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams
title_short Loss of genes related to Nucleotide Excision Repair (NER) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams
title_sort loss of genes related to nucleotide excision repair (ner) and implications for reductive genome evolution in symbionts of deep-sea vesicomyid clams
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310779/
https://www.ncbi.nlm.nih.gov/pubmed/28199404
http://dx.doi.org/10.1371/journal.pone.0171274
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