Evidence map›Paper›PMID 29914365›Full record

ArticleBMC genomics2018

The genome of Rhizophagus clarus HR1 reveals a common genetic basis for auxotrophy among arbuscular mycorrhizal fungi.

Yuuki Kobayashi, Taro Maeda, Katsushi Yamaguchi, Hiromu Kameoka, Sachiko Tanaka, Tatsuhiro Ezawa, Shuji Shigenobu, Masayoshi Kawaguchi

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
17.2field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 142 citations in OpenAlex.

  1. Review
  2. Article
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  4. Asymbiotic Growth of Arbuscular Mycorrhizal Fungi.Methods in molecular biology (Clifton, N.J.) · 2026
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  16. Characterization of the complete mitochondrial genome ofMitochondrial DNA. Part B, Resources · 2024
    Article
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  19. Review
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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

8 authors at 3 institutions in 1 country.

Yuuki KobayashiDivision of Symbiotic Systems, National Institute for Basic Biology, Okazaki, Japan.
Taro MaedaDivision of Symbiotic Systems, National Institute for Basic Biology, Okazaki, Japan.
Katsushi YamaguchiFunctional Genomics Facility, National Institute for Basic Biology, Okazaki, Japan.
Hiromu KameokaDivision of Symbiotic Systems, National Institute for Basic Biology, Okazaki, Japan.
Sachiko TanakaDivision of Symbiotic Systems, National Institute for Basic Biology, Okazaki, Japan.
Tatsuhiro EzawaResearch Faculty of Agriculture, Hokkaido University, Sapporo, Japan.
Shuji ShigenobuFunctional Genomics Facility, National Institute for Basic Biology, Okazaki, Japan.
Masayoshi KawaguchiDivision of Symbiotic Systems, National Institute for Basic Biology, Okazaki, Japan. masayosi@nibb.ac.jp.
National Institute for Basic Biology · JPHokkaido University · JPThe Graduate University for Advanced Studies, SOKENDAI · JP

Funding

Accelerated Innovation Research Initiative Turning Top Science and Ideas into High-Impact Values JPMJAC1403
6 · The paper itself

Abstract

backgroundMycorrhizal symbiosis is one of the most fundamental types of mutualistic plant-microbe interaction. Among the many classes of mycorrhizae, the arbuscular mycorrhizae have the most general symbiotic style and the longest history. However, the genomes of arbuscular mycorrhizal (AM) fungi are not well characterized due to difficulties in cultivation and genetic analysis. In this study, we sequenced the genome of the AM fungus Rhizophagus clarus HR1, compared the sequence with the genome sequence of the model species R. irregularis, and checked for missing genes that encode enzymes in metabolic pathways related to their obligate biotrophy.

resultsIn the genome of R. clarus, we confirmed the absence of cytosolic fatty acid synthase (FAS), whereas all mitochondrial FAS components were present. A KEGG pathway map identified the absence of genes encoding enzymes for several other metabolic pathways in the two AM fungi, including thiamine biosynthesis and the conversion of vitamin B6 derivatives. We also found that a large proportion of the genes encoding glucose-producing polysaccharide hydrolases, that are present even in ectomycorrhizal fungi, also appear to be absent in AM fungi.

conclusionsIn this study, we found several new genes that are absent from the genomes of AM fungi in addition to the genes previously identified as missing. Missing genes for enzymes in primary metabolic pathways imply that AM fungi may have a higher dependency on host plants than other biotrophic fungi. These missing metabolic pathways provide a genetic basis to explore the physiological characteristics and auxotrophy of AM fungi.

Indexed as

Gene Expression Regulation, PlantGenome, FungalComputational BiologyDaucus carotaDNA, FungalFungal ProteinsGlomeromycotaHigh-Throughput Nucleotide SequencingMycorrhizaePlant RootsSequence Analysis, DNASymbiosisDNA, FungalFungal ProteinsArbuscular mycorrhizaAuxotrophyComparative genomicsde novo genome sequencingObligate symbiosisRhizophagus clarus

Identifiers

PMID29914365
PMCPMC6007072
OpenAlexW2807716495

What OpenQuestion holds

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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.