Evidence map›Paper›PMID 36999556›Full record

ArticleG3 (Bethesda, Md.)2023

A highly contiguous genome assembly reveals sources of genomic novelty in the symbiotic fungus Rhizophagus irregularis.

Bethan F Manley, Jaruwatana S Lotharukpong, Josué Barrera-Redondo, Theo Llewellyn, Gokalp Yildirir, Jana Sperschneider, Nicolas Corradi, Uta Paszkowski, Eric A Miska, Alexandra Dallaire

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
9.9field-weighted citation impact, top 2% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

11 citing papers in PubMed, 25 citations in OpenAlex.

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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

10 authors at 7 institutions in 5 countries.

Bethan F ManleySPUN|Society for the Protection of Underground Networks, 3500 South DuPont Highway, Suite EI-101, Dover, DE 19901, USA.
Jaruwatana S LotharukpongDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, Tübingen 72076, Germany.
Josué Barrera-RedondoDepartment of Algal Development and Evolution, Max Planck Institute for Biology, Max-Planck-Ring 5, Tübingen 72076, Germany.
Theo LlewellynComparative Fungal Biology, Royal Botanic Gardens Kew, Jodrell Laboratory, Richmond TW9 3DS, UK.
Gokalp YildirirDepartment of Biology, University of Ottawa, Ottawa, ON, Canada K1N 6N5.
Jana SperschneiderAgriculture and Food, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia.
Nicolas CorradiDepartment of Biology, University of Ottawa, Ottawa, ON, Canada K1N 6N5.
Uta PaszkowskiCrop Science Centre, Department of Plant Sciences, University of Cambridge, Cambridge CB3 0LE, UK.
Eric A MiskaGurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.
Alexandra DallaireGurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK.
Royal Botanic Gardens, Kew · GBUniversity of Cambridge · GBUniversity of Ottawa · CACommonwealth Scientific and Industrial Research Organisation · AUDuPont (United States) · USMax Planck Institute for Biology · DEMax Planck Institute for Developmental Biology · DE

Funding

Cancer Research UK C13474/A18583Cancer Research UK C6946/A14492European Research Council 864038Wellcome TrustWellcome Trust 092096/Z/10/ZWellcome Trust 219475/Z/19/Z
6 · The paper itself

Abstract

The root systems of most plant species are aided by the soil-foraging capacities of symbiotic arbuscular mycorrhizal (AM) fungi of the Glomeromycotina subphylum. Despite recent advances in our knowledge of the ecology and molecular biology of this mutualistic symbiosis, our understanding of the AM fungi genome biology is just emerging. Presented here is a close to T2T genome assembly of the model AM fungus Rhizophagus irregularis DAOM197198, achieved through Nanopore long-read DNA sequencing and Hi-C data. This haploid genome assembly of R. irregularis, alongside short- and long-read RNA-Sequencing data, was used to produce a comprehensive annotation catalog of gene models, repetitive elements, small RNA loci, and DNA cytosine methylome. A phylostratigraphic gene age inference framework revealed that the birth of genes associated with nutrient transporter activity and transmembrane ion transport systems predates the emergence of Glomeromycotina. While nutrient cycling in AM fungi relies on genes that existed in ancestor lineages, a burst of Glomeromycotina-restricted genetic innovation is also detected. Analysis of the chromosomal distribution of genetic and epigenetic features highlights evolutionarily young genomic regions that produce abundant small RNAs, suggesting active RNA-based monitoring of genetic sequences surrounding recently evolved genes. This chromosome-scale view of the genome of an AM fungus genome reveals previously unexplored sources of genomic novelty in an organism evolving under an obligate symbiotic life cycle.

Indexed as

GlomeromycotaMycorrhizaeFungiGenomicsRNASymbiosisRNAAMFarbuscular mycorrhizal fungichromosome-scalegene birthgenome assemblygenome evolution

Identifiers

PMID36999556
PMCPMC10234402
OpenAlexW4362458910

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Registered trials

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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.