Evidence map›Paper›PMID 38811885›Full record

ArticleBMC genomics2024

Evolutionary history of arbuscular mycorrhizal fungi and genomic signatures of obligate symbiosis.

Anna Rosling, Shadi Eshghi Sahraei, Faheema Kalsoom Khan, Alessandro Desirò, Abigail E Bryson, Stephen J Mondo, Igor V Grigoriev, Gregory Bonito, Marisol Sánchez-García

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Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Anna Rosling *Department of Ecology and Genetics, Uppsala University, Uppsala, Sweden. Anna.Rosling@ebc.uu.se.
Shadi Eshghi Sahraei *Department of Ecology and Genetics, Uppsala University, Uppsala, Sweden.
Faheema Kalsoom KhanDepartment of Organismal Biology, Uppsala University, Uppsala, Sweden.
Alessandro DesiròDepartment of Plant Soil and Microbial Sciences, Michigan State University, East Lansing, MI, USA.
Abigail E BrysonDepartment of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI, USA.
Stephen J MondoDepartment of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National laboratory, Berkeley, CA, USA.
Igor V GrigorievDepartment of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National laboratory, Berkeley, CA, USA.
Gregory BonitoDepartment of Plant Soil and Microbial Sciences, Michigan State University, East Lansing, MI, USA.
Marisol Sánchez-GarcíaDepartment of Ecology and Genetics, Uppsala University, Uppsala, Sweden. marisol.sanchez.garcia@slu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe colonization of land and the diversification of terrestrial plants is intimately linked to the evolutionary history of their symbiotic fungal partners. Extant representatives of these fungal lineages include mutualistic plant symbionts, the arbuscular mycorrhizal (AM) fungi in Glomeromycota and fine root endophytes in Endogonales (Mucoromycota), as well as fungi with saprotrophic, pathogenic and endophytic lifestyles. These fungal groups separate into three monophyletic lineages but their evolutionary relationships remain enigmatic confounding ancestral reconstructions. Their taxonomic ranks are currently fluid.

resultsIn this study, we recognize these three monophyletic linages as phyla, and use a balanced taxon sampling and broad taxonomic representation for phylogenomic analysis that rejects a hard polytomy and resolves Glomeromycota as sister to a clade composed of Mucoromycota and Mortierellomycota. Low copy numbers of genes associated with plant cell wall degradation could not be assigned to the transition to a plant symbiotic lifestyle but appears to be an ancestral phylogenetic signal. Both plant symbiotic lineages, Glomeromycota and Endogonales, lack numerous thiamine metabolism genes but the lack of fatty acid synthesis genes is specific to AM fungi. Many genes previously thought to be missing specifically in Glomeromycota are either missing in all analyzed phyla, or in some cases, are actually present in some of the analyzed AM fungal lineages, e.g. the high affinity phosphorus transporter Pho89.

conclusionBased on a broad taxon sampling of fungal genomes we present a well-supported phylogeny for AM fungi and their sister lineages. We show that among these lineages, two independent evolutionary transitions to mutualistic plant symbiosis happened in a genomic background profoundly different from that known from the emergence of ectomycorrhizal fungi in Dikarya. These results call for further reevaluation of genomic signatures associated with plant symbiosis.

Indexed as

GenomicsMycorrhizaePhylogenySymbiosisEvolution, MolecularGenome, FungalGlomeromycotaPlantsEndogonalesEvolutionGlomeromycotaPhylogenyPlant-fungal symbiosis

Identifiers

PMID38811885
PMCPMC11134847

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.