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The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes
Phosphorothioate (PT) modification by the dnd gene cluster is the first identified DNA backbone modification and constitute an epigenetic system with multiple functions, including antioxidant ability, restriction modification, and virus resistance. Despite these advantages for hosting dnd systems, t...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569181/ https://www.ncbi.nlm.nih.gov/pubmed/34737280 http://dx.doi.org/10.1038/s41467-021-26636-7 |
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author | Jian, Huahua Xu, Guanpeng Yi, Yi Hao, Yali Wang, Yinzhao Xiong, Lei Wang, Siyuan Liu, Shunzhang Meng, Canxing Wang, Jiahua Zhang, Yue Chen, Chao Feng, Xiaoyuan Luo, Haiwei Zhang, Hao Zhang, Xingguo Wang, Lianrong Wang, Zhijun Deng, Zixin Xiao, Xiang |
author_facet | Jian, Huahua Xu, Guanpeng Yi, Yi Hao, Yali Wang, Yinzhao Xiong, Lei Wang, Siyuan Liu, Shunzhang Meng, Canxing Wang, Jiahua Zhang, Yue Chen, Chao Feng, Xiaoyuan Luo, Haiwei Zhang, Hao Zhang, Xingguo Wang, Lianrong Wang, Zhijun Deng, Zixin Xiao, Xiang |
author_sort | Jian, Huahua |
collection | PubMed |
description | Phosphorothioate (PT) modification by the dnd gene cluster is the first identified DNA backbone modification and constitute an epigenetic system with multiple functions, including antioxidant ability, restriction modification, and virus resistance. Despite these advantages for hosting dnd systems, they are surprisingly distributed sporadically among contemporary prokaryotic genomes. To address this ecological paradox, we systematically investigate the occurrence and phylogeny of dnd systems, and they are suggested to have originated in ancient Cyanobacteria after the Great Oxygenation Event. Interestingly, the occurrence of dnd systems and prophages is significantly negatively correlated. Further, we experimentally confirm that PT modification activates the filamentous phage SW1 by altering the binding affinity of repressor and the transcription level of its encoding gene. Competition assays, concurrent epigenomic and transcriptomic sequencing subsequently show that PT modification affects the expression of a variety of metabolic genes, which reduces the competitive fitness of the marine bacterium Shewanella piezotolerans WP3. Our findings strongly suggest that a series of negative effects on microorganisms caused by dnd systems limit horizontal gene transfer, thus leading to their sporadic distribution. Overall, our study reveals putative evolutionary scenario of the dnd system and provides novel insights into the physiological and ecological influences of PT modification. |
format | Online Article Text |
id | pubmed-8569181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85691812021-11-15 The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes Jian, Huahua Xu, Guanpeng Yi, Yi Hao, Yali Wang, Yinzhao Xiong, Lei Wang, Siyuan Liu, Shunzhang Meng, Canxing Wang, Jiahua Zhang, Yue Chen, Chao Feng, Xiaoyuan Luo, Haiwei Zhang, Hao Zhang, Xingguo Wang, Lianrong Wang, Zhijun Deng, Zixin Xiao, Xiang Nat Commun Article Phosphorothioate (PT) modification by the dnd gene cluster is the first identified DNA backbone modification and constitute an epigenetic system with multiple functions, including antioxidant ability, restriction modification, and virus resistance. Despite these advantages for hosting dnd systems, they are surprisingly distributed sporadically among contemporary prokaryotic genomes. To address this ecological paradox, we systematically investigate the occurrence and phylogeny of dnd systems, and they are suggested to have originated in ancient Cyanobacteria after the Great Oxygenation Event. Interestingly, the occurrence of dnd systems and prophages is significantly negatively correlated. Further, we experimentally confirm that PT modification activates the filamentous phage SW1 by altering the binding affinity of repressor and the transcription level of its encoding gene. Competition assays, concurrent epigenomic and transcriptomic sequencing subsequently show that PT modification affects the expression of a variety of metabolic genes, which reduces the competitive fitness of the marine bacterium Shewanella piezotolerans WP3. Our findings strongly suggest that a series of negative effects on microorganisms caused by dnd systems limit horizontal gene transfer, thus leading to their sporadic distribution. Overall, our study reveals putative evolutionary scenario of the dnd system and provides novel insights into the physiological and ecological influences of PT modification. Nature Publishing Group UK 2021-11-04 /pmc/articles/PMC8569181/ /pubmed/34737280 http://dx.doi.org/10.1038/s41467-021-26636-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jian, Huahua Xu, Guanpeng Yi, Yi Hao, Yali Wang, Yinzhao Xiong, Lei Wang, Siyuan Liu, Shunzhang Meng, Canxing Wang, Jiahua Zhang, Yue Chen, Chao Feng, Xiaoyuan Luo, Haiwei Zhang, Hao Zhang, Xingguo Wang, Lianrong Wang, Zhijun Deng, Zixin Xiao, Xiang The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes |
title | The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes |
title_full | The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes |
title_fullStr | The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes |
title_full_unstemmed | The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes |
title_short | The origin and impeded dissemination of the DNA phosphorothioation system in prokaryotes |
title_sort | origin and impeded dissemination of the dna phosphorothioation system in prokaryotes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569181/ https://www.ncbi.nlm.nih.gov/pubmed/34737280 http://dx.doi.org/10.1038/s41467-021-26636-7 |
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