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A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order

Self-recognition underlies sociality in many group-living organisms. In bacteria, cells use various strategies to recognize kin to form social groups and, in some cases, to transition into multicellular life. One strategy relies on a single genetic locus that encodes a variable phenotypic tag (“gree...

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Autores principales: Cao, Pengbo, Wei, Xueming, Awal, Ram Prasad, Müller, Rolf, Wall, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372800/
https://www.ncbi.nlm.nih.gov/pubmed/30755513
http://dx.doi.org/10.1128/mBio.02751-18
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author Cao, Pengbo
Wei, Xueming
Awal, Ram Prasad
Müller, Rolf
Wall, Daniel
author_facet Cao, Pengbo
Wei, Xueming
Awal, Ram Prasad
Müller, Rolf
Wall, Daniel
author_sort Cao, Pengbo
collection PubMed
description Self-recognition underlies sociality in many group-living organisms. In bacteria, cells use various strategies to recognize kin to form social groups and, in some cases, to transition into multicellular life. One strategy relies on a single genetic locus that encodes a variable phenotypic tag (“greenbeard”) for recognizing other tag bearers. Previously, we discovered a polymorphic cell surface receptor called TraA that directs self-identification through homotypic interactions in the social bacterium Myxococcus xanthus. Recognition by TraA leads to cellular resource sharing in a process called outer membrane exchange (OME). A second gene in the traA operon, traB, is also required for OME but is not involved in recognition. Our prior studies of TraA identified only six recognition groups among closely related M. xanthus isolates. Here we hypothesize that the number of traA polymorphisms and, consequently, the diversity of recognition in wild isolates are much greater. To test this hypothesis, we expand the scope of TraA characterization to the order Myxococcales. From genomic sequences within the three suborders of Myxococcales, we identified 90 traA orthologs. Sequence analyses and functional characterization of traAB loci suggest that OME is well maintained among diverse myxobacterial taxonomic groups. Importantly, TraA orthologs are highly polymorphic within their variable domain, the region that confers selectivity in self-recognition. We experimentally defined 10 distinct recognition groups and, based on phylogenetic and experimental analyses, predicted >60 recognition groups among the 90 traA alleles. Taken together, our findings revealed a widespread greenbeard locus that mediates the diversity of self-recognition across the order Myxococcales.
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spelling pubmed-63728002019-02-22 A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order Cao, Pengbo Wei, Xueming Awal, Ram Prasad Müller, Rolf Wall, Daniel mBio Research Article Self-recognition underlies sociality in many group-living organisms. In bacteria, cells use various strategies to recognize kin to form social groups and, in some cases, to transition into multicellular life. One strategy relies on a single genetic locus that encodes a variable phenotypic tag (“greenbeard”) for recognizing other tag bearers. Previously, we discovered a polymorphic cell surface receptor called TraA that directs self-identification through homotypic interactions in the social bacterium Myxococcus xanthus. Recognition by TraA leads to cellular resource sharing in a process called outer membrane exchange (OME). A second gene in the traA operon, traB, is also required for OME but is not involved in recognition. Our prior studies of TraA identified only six recognition groups among closely related M. xanthus isolates. Here we hypothesize that the number of traA polymorphisms and, consequently, the diversity of recognition in wild isolates are much greater. To test this hypothesis, we expand the scope of TraA characterization to the order Myxococcales. From genomic sequences within the three suborders of Myxococcales, we identified 90 traA orthologs. Sequence analyses and functional characterization of traAB loci suggest that OME is well maintained among diverse myxobacterial taxonomic groups. Importantly, TraA orthologs are highly polymorphic within their variable domain, the region that confers selectivity in self-recognition. We experimentally defined 10 distinct recognition groups and, based on phylogenetic and experimental analyses, predicted >60 recognition groups among the 90 traA alleles. Taken together, our findings revealed a widespread greenbeard locus that mediates the diversity of self-recognition across the order Myxococcales. American Society for Microbiology 2019-02-12 /pmc/articles/PMC6372800/ /pubmed/30755513 http://dx.doi.org/10.1128/mBio.02751-18 Text en Copyright © 2019 Cao et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Cao, Pengbo
Wei, Xueming
Awal, Ram Prasad
Müller, Rolf
Wall, Daniel
A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order
title A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order
title_full A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order
title_fullStr A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order
title_full_unstemmed A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order
title_short A Highly Polymorphic Receptor Governs Many Distinct Self-Recognition Types within the Myxococcales Order
title_sort highly polymorphic receptor governs many distinct self-recognition types within the myxococcales order
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372800/
https://www.ncbi.nlm.nih.gov/pubmed/30755513
http://dx.doi.org/10.1128/mBio.02751-18
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