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The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling

The rise of oxygen on the early Earth about 2.4 billion years ago reorganized the redox cycle of harmful metal(loids), including that of arsenic, which doubtlessly imposed substantial barriers to the physiology and diversification of life. Evaluating the adaptive biological responses to these enviro...

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Autores principales: Chen, Song-Can, Sun, Guo-Xin, Yan, Yu, Konstantinidis, Konstantinos T., Zhang, Si-Yu, Deng, Ye, Li, Xiao-Min, Cui, Hui-Ling, Musat, Florin, Popp, Denny, Rosen, Barry P., Zhu, Yong-Guan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229686/
https://www.ncbi.nlm.nih.gov/pubmed/32350143
http://dx.doi.org/10.1073/pnas.2001063117
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author Chen, Song-Can
Sun, Guo-Xin
Yan, Yu
Konstantinidis, Konstantinos T.
Zhang, Si-Yu
Deng, Ye
Li, Xiao-Min
Cui, Hui-Ling
Musat, Florin
Popp, Denny
Rosen, Barry P.
Zhu, Yong-Guan
author_facet Chen, Song-Can
Sun, Guo-Xin
Yan, Yu
Konstantinidis, Konstantinos T.
Zhang, Si-Yu
Deng, Ye
Li, Xiao-Min
Cui, Hui-Ling
Musat, Florin
Popp, Denny
Rosen, Barry P.
Zhu, Yong-Guan
author_sort Chen, Song-Can
collection PubMed
description The rise of oxygen on the early Earth about 2.4 billion years ago reorganized the redox cycle of harmful metal(loids), including that of arsenic, which doubtlessly imposed substantial barriers to the physiology and diversification of life. Evaluating the adaptive biological responses to these environmental challenges is inherently difficult because of the paucity of fossil records. Here we applied molecular clock analyses to 13 gene families participating in principal pathways of arsenic resistance and cycling, to explore the nature of early arsenic biogeocycles and decipher feedbacks associated with planetary oxygenation. Our results reveal the advent of nascent arsenic resistance systems under the anoxic environment predating the Great Oxidation Event (GOE), with the primary function of detoxifying reduced arsenic compounds that were abundant in Archean environments. To cope with the increased toxicity of oxidized arsenic species that occurred as oxygen built up in Earth’s atmosphere, we found that parts of preexisting detoxification systems for trivalent arsenicals were merged with newly emerged pathways that originated via convergent evolution. Further expansion of arsenic resistance systems was made feasible by incorporation of oxygen-dependent enzymatic pathways into the detoxification network. These genetic innovations, together with adaptive responses to other redox-sensitive metals, provided organisms with novel mechanisms for adaption to changes in global biogeocycles that emerged as a consequence of the GOE.
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spelling pubmed-72296862020-05-26 The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling Chen, Song-Can Sun, Guo-Xin Yan, Yu Konstantinidis, Konstantinos T. Zhang, Si-Yu Deng, Ye Li, Xiao-Min Cui, Hui-Ling Musat, Florin Popp, Denny Rosen, Barry P. Zhu, Yong-Guan Proc Natl Acad Sci U S A Biological Sciences The rise of oxygen on the early Earth about 2.4 billion years ago reorganized the redox cycle of harmful metal(loids), including that of arsenic, which doubtlessly imposed substantial barriers to the physiology and diversification of life. Evaluating the adaptive biological responses to these environmental challenges is inherently difficult because of the paucity of fossil records. Here we applied molecular clock analyses to 13 gene families participating in principal pathways of arsenic resistance and cycling, to explore the nature of early arsenic biogeocycles and decipher feedbacks associated with planetary oxygenation. Our results reveal the advent of nascent arsenic resistance systems under the anoxic environment predating the Great Oxidation Event (GOE), with the primary function of detoxifying reduced arsenic compounds that were abundant in Archean environments. To cope with the increased toxicity of oxidized arsenic species that occurred as oxygen built up in Earth’s atmosphere, we found that parts of preexisting detoxification systems for trivalent arsenicals were merged with newly emerged pathways that originated via convergent evolution. Further expansion of arsenic resistance systems was made feasible by incorporation of oxygen-dependent enzymatic pathways into the detoxification network. These genetic innovations, together with adaptive responses to other redox-sensitive metals, provided organisms with novel mechanisms for adaption to changes in global biogeocycles that emerged as a consequence of the GOE. National Academy of Sciences 2020-05-12 2020-04-29 /pmc/articles/PMC7229686/ /pubmed/32350143 http://dx.doi.org/10.1073/pnas.2001063117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Chen, Song-Can
Sun, Guo-Xin
Yan, Yu
Konstantinidis, Konstantinos T.
Zhang, Si-Yu
Deng, Ye
Li, Xiao-Min
Cui, Hui-Ling
Musat, Florin
Popp, Denny
Rosen, Barry P.
Zhu, Yong-Guan
The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling
title The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling
title_full The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling
title_fullStr The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling
title_full_unstemmed The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling
title_short The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling
title_sort great oxidation event expanded the genetic repertoire of arsenic metabolism and cycling
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229686/
https://www.ncbi.nlm.nih.gov/pubmed/32350143
http://dx.doi.org/10.1073/pnas.2001063117
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