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Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi

Arbuscular mycorrhizal fungi (AMF) are a group of soil microorganisms that establish symbioses with the vast majority of land plants. To date, generation of AMF coding information has been limited to model genera that grow well axenically; Rhizoglomus and Gigaspora. Meanwhile, data on the functional...

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Autores principales: Beaudet, Denis, Chen, Eric C H, Mathieu, Stephanie, Yildirir, Gokalp, Ndikumana, Steve, Dalpé, Yolande, Séguin, Sylvie, Farinelli, Laurent, Stajich, Jason E, Corradi, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909441/
https://www.ncbi.nlm.nih.gov/pubmed/29211832
http://dx.doi.org/10.1093/dnares/dsx051
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author Beaudet, Denis
Chen, Eric C H
Mathieu, Stephanie
Yildirir, Gokalp
Ndikumana, Steve
Dalpé, Yolande
Séguin, Sylvie
Farinelli, Laurent
Stajich, Jason E
Corradi, Nicolas
author_facet Beaudet, Denis
Chen, Eric C H
Mathieu, Stephanie
Yildirir, Gokalp
Ndikumana, Steve
Dalpé, Yolande
Séguin, Sylvie
Farinelli, Laurent
Stajich, Jason E
Corradi, Nicolas
author_sort Beaudet, Denis
collection PubMed
description Arbuscular mycorrhizal fungi (AMF) are a group of soil microorganisms that establish symbioses with the vast majority of land plants. To date, generation of AMF coding information has been limited to model genera that grow well axenically; Rhizoglomus and Gigaspora. Meanwhile, data on the functional gene repertoire of most AMF families is non-existent. Here, we provide primary large-scale transcriptome data from eight poorly studied AMF species (Acaulospora morrowiae, Diversispora versiforme, Scutellospora calospora, Racocetra castanea, Paraglomus brasilianum, Ambispora leptoticha, Claroideoglomus claroideum and Funneliformis mosseae) using ultra-low input ribonucleic acid (RNA)-seq approaches. Our analyses reveals that quiescent spores of many AMF species harbour a diverse functional diversity and solidify known evolutionary relationships within the group. Our findings demonstrate that RNA-seq data obtained from low-input RNA are reliable in comparison to conventional RNA-seq experiments. Thus, our methodology can potentially be used to deepen our understanding of fungal microbial function and phylogeny using minute amounts of RNA material.
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spelling pubmed-59094412018-04-24 Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi Beaudet, Denis Chen, Eric C H Mathieu, Stephanie Yildirir, Gokalp Ndikumana, Steve Dalpé, Yolande Séguin, Sylvie Farinelli, Laurent Stajich, Jason E Corradi, Nicolas DNA Res Full Papers Arbuscular mycorrhizal fungi (AMF) are a group of soil microorganisms that establish symbioses with the vast majority of land plants. To date, generation of AMF coding information has been limited to model genera that grow well axenically; Rhizoglomus and Gigaspora. Meanwhile, data on the functional gene repertoire of most AMF families is non-existent. Here, we provide primary large-scale transcriptome data from eight poorly studied AMF species (Acaulospora morrowiae, Diversispora versiforme, Scutellospora calospora, Racocetra castanea, Paraglomus brasilianum, Ambispora leptoticha, Claroideoglomus claroideum and Funneliformis mosseae) using ultra-low input ribonucleic acid (RNA)-seq approaches. Our analyses reveals that quiescent spores of many AMF species harbour a diverse functional diversity and solidify known evolutionary relationships within the group. Our findings demonstrate that RNA-seq data obtained from low-input RNA are reliable in comparison to conventional RNA-seq experiments. Thus, our methodology can potentially be used to deepen our understanding of fungal microbial function and phylogeny using minute amounts of RNA material. Oxford University Press 2018-04 2017-12-02 /pmc/articles/PMC5909441/ /pubmed/29211832 http://dx.doi.org/10.1093/dnares/dsx051 Text en © The Author 2017. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Full Papers
Beaudet, Denis
Chen, Eric C H
Mathieu, Stephanie
Yildirir, Gokalp
Ndikumana, Steve
Dalpé, Yolande
Séguin, Sylvie
Farinelli, Laurent
Stajich, Jason E
Corradi, Nicolas
Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi
title Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi
title_full Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi
title_fullStr Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi
title_full_unstemmed Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi
title_short Ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi
title_sort ultra-low input transcriptomics reveal the spore functional content and phylogenetic affiliations of poorly studied arbuscular mycorrhizal fungi
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909441/
https://www.ncbi.nlm.nih.gov/pubmed/29211832
http://dx.doi.org/10.1093/dnares/dsx051
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