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Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor

Functional divergence of paralogs following gene duplication is one of the mechanisms leading to evolution of novel pathways and traits. Here we show that divergence of Lys11 and Nfr5 LysM receptor kinase paralogs of Lotus japonicus has affected their specificity for lipochitooligosaccharides (LCOs)...

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Autores principales: Rasmussen, S. R., Füchtbauer, W., Novero, M., Volpe, V., Malkov, N., Genre, A., Bonfante, P., Stougaard, J., Radutoiu, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951684/
https://www.ncbi.nlm.nih.gov/pubmed/27435342
http://dx.doi.org/10.1038/srep29733
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author Rasmussen, S. R.
Füchtbauer, W.
Novero, M.
Volpe, V.
Malkov, N.
Genre, A.
Bonfante, P.
Stougaard, J.
Radutoiu, S.
author_facet Rasmussen, S. R.
Füchtbauer, W.
Novero, M.
Volpe, V.
Malkov, N.
Genre, A.
Bonfante, P.
Stougaard, J.
Radutoiu, S.
author_sort Rasmussen, S. R.
collection PubMed
description Functional divergence of paralogs following gene duplication is one of the mechanisms leading to evolution of novel pathways and traits. Here we show that divergence of Lys11 and Nfr5 LysM receptor kinase paralogs of Lotus japonicus has affected their specificity for lipochitooligosaccharides (LCOs) decorations, while the innate capacity to recognize and induce a downstream signalling after perception of rhizobial LCOs (Nod factors) was maintained. Regardless of this conserved ability, Lys11 was found neither expressed, nor essential during nitrogen-fixing symbiosis, providing an explanation for the determinant role of Nfr5 gene during Lotus-rhizobia interaction. Lys11 was expressed in root cortex cells associated with intraradical colonizing arbuscular mycorrhizal fungi. Detailed analyses of lys11 single and nfr1nfr5lys11 triple mutants revealed a functional arbuscular mycorrhizal symbiosis, indicating that Lys11 alone, or its possible shared function with the Nod factor receptors is not essential for the presymbiotic phases of AM symbiosis. Hence, both subfunctionalization and specialization appear to have shaped the function of these paralogs where Lys11 acts as an AM-inducible gene, possibly to fine-tune later stages of this interaction.
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spelling pubmed-49516842016-07-26 Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor Rasmussen, S. R. Füchtbauer, W. Novero, M. Volpe, V. Malkov, N. Genre, A. Bonfante, P. Stougaard, J. Radutoiu, S. Sci Rep Article Functional divergence of paralogs following gene duplication is one of the mechanisms leading to evolution of novel pathways and traits. Here we show that divergence of Lys11 and Nfr5 LysM receptor kinase paralogs of Lotus japonicus has affected their specificity for lipochitooligosaccharides (LCOs) decorations, while the innate capacity to recognize and induce a downstream signalling after perception of rhizobial LCOs (Nod factors) was maintained. Regardless of this conserved ability, Lys11 was found neither expressed, nor essential during nitrogen-fixing symbiosis, providing an explanation for the determinant role of Nfr5 gene during Lotus-rhizobia interaction. Lys11 was expressed in root cortex cells associated with intraradical colonizing arbuscular mycorrhizal fungi. Detailed analyses of lys11 single and nfr1nfr5lys11 triple mutants revealed a functional arbuscular mycorrhizal symbiosis, indicating that Lys11 alone, or its possible shared function with the Nod factor receptors is not essential for the presymbiotic phases of AM symbiosis. Hence, both subfunctionalization and specialization appear to have shaped the function of these paralogs where Lys11 acts as an AM-inducible gene, possibly to fine-tune later stages of this interaction. Nature Publishing Group 2016-07-20 /pmc/articles/PMC4951684/ /pubmed/27435342 http://dx.doi.org/10.1038/srep29733 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Rasmussen, S. R.
Füchtbauer, W.
Novero, M.
Volpe, V.
Malkov, N.
Genre, A.
Bonfante, P.
Stougaard, J.
Radutoiu, S.
Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor
title Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor
title_full Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor
title_fullStr Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor
title_full_unstemmed Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor
title_short Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor
title_sort intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4951684/
https://www.ncbi.nlm.nih.gov/pubmed/27435342
http://dx.doi.org/10.1038/srep29733
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