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MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria

MamA is a highly conserved protein found in magnetotactic bacteria (MTB), a diverse group of prokaryotes capable of navigating according to magnetic fields – an ability known as magnetotaxis. Questions surround the acquisition of this magnetic navigation ability; namely, whether it arose through hor...

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Autores principales: Zeytuni, Natalie, Cronin, Samuel, Lefèvre, Christopher T., Arnoux, Pascal, Baran, Dror, Shtein, Zvi, Davidov, Geula, Zarivach, Raz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482739/
https://www.ncbi.nlm.nih.gov/pubmed/26114501
http://dx.doi.org/10.1371/journal.pone.0130394
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author Zeytuni, Natalie
Cronin, Samuel
Lefèvre, Christopher T.
Arnoux, Pascal
Baran, Dror
Shtein, Zvi
Davidov, Geula
Zarivach, Raz
author_facet Zeytuni, Natalie
Cronin, Samuel
Lefèvre, Christopher T.
Arnoux, Pascal
Baran, Dror
Shtein, Zvi
Davidov, Geula
Zarivach, Raz
author_sort Zeytuni, Natalie
collection PubMed
description MamA is a highly conserved protein found in magnetotactic bacteria (MTB), a diverse group of prokaryotes capable of navigating according to magnetic fields – an ability known as magnetotaxis. Questions surround the acquisition of this magnetic navigation ability; namely, whether it arose through horizontal or vertical gene transfer. Though its exact function is unknown, MamA surrounds the magnetosome, the magnetic organelle embedding a biomineralised nanoparticle and responsible for magnetotaxis. Several structures for MamA from a variety of species have been determined and show a high degree of structural similarity. By determining the structure of MamA from Desulfovibrio magneticus RS-1 using X-ray crystallography, we have opened up the structure-sequence landscape. As such, this allows us to perform structural- and phylogenetic-based analyses using a variety of previously determined MamA from a diverse range of MTB species across various phylogenetic groups. We found that MamA has remained remarkably constant throughout evolution with minimal change between different taxa despite sequence variations. These findings, coupled with the generation of phylogenetic trees using both amino acid sequences and 16S rRNA, indicate that magnetotaxis likely did not spread via horizontal gene transfer and instead has a significantly earlier, primordial origin.
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spelling pubmed-44827392015-06-29 MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria Zeytuni, Natalie Cronin, Samuel Lefèvre, Christopher T. Arnoux, Pascal Baran, Dror Shtein, Zvi Davidov, Geula Zarivach, Raz PLoS One Research Article MamA is a highly conserved protein found in magnetotactic bacteria (MTB), a diverse group of prokaryotes capable of navigating according to magnetic fields – an ability known as magnetotaxis. Questions surround the acquisition of this magnetic navigation ability; namely, whether it arose through horizontal or vertical gene transfer. Though its exact function is unknown, MamA surrounds the magnetosome, the magnetic organelle embedding a biomineralised nanoparticle and responsible for magnetotaxis. Several structures for MamA from a variety of species have been determined and show a high degree of structural similarity. By determining the structure of MamA from Desulfovibrio magneticus RS-1 using X-ray crystallography, we have opened up the structure-sequence landscape. As such, this allows us to perform structural- and phylogenetic-based analyses using a variety of previously determined MamA from a diverse range of MTB species across various phylogenetic groups. We found that MamA has remained remarkably constant throughout evolution with minimal change between different taxa despite sequence variations. These findings, coupled with the generation of phylogenetic trees using both amino acid sequences and 16S rRNA, indicate that magnetotaxis likely did not spread via horizontal gene transfer and instead has a significantly earlier, primordial origin. Public Library of Science 2015-06-26 /pmc/articles/PMC4482739/ /pubmed/26114501 http://dx.doi.org/10.1371/journal.pone.0130394 Text en © 2015 Zeytuni 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zeytuni, Natalie
Cronin, Samuel
Lefèvre, Christopher T.
Arnoux, Pascal
Baran, Dror
Shtein, Zvi
Davidov, Geula
Zarivach, Raz
MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria
title MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria
title_full MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria
title_fullStr MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria
title_full_unstemmed MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria
title_short MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria
title_sort mama as a model protein for structure-based insight into the evolutionary origins of magnetotactic bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482739/
https://www.ncbi.nlm.nih.gov/pubmed/26114501
http://dx.doi.org/10.1371/journal.pone.0130394
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