Evidence map›Paper›PMID 26872771›Full record

ArticleGenome biology and evolution2016

A Tale of Genome Compartmentalization: The Evolution of Virulence Clusters in Smut Fungi.

Julien Y Dutheil, Gertrud Mannhaupt, Gabriel Schweizer, Christian M K Sieber, Martin Münsterkötter, Ulrich Güldener, Jan Schirawski, Regine Kahmann

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
15.7field-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

67 citing papers in PubMed, 131 citations in OpenAlex.

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  18. TheJournal of fungi (Basel, Switzerland) · 2022
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  19. Squalene Monooxygenase GeneJournal of fungi (Basel, Switzerland) · 2022
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  20. Article

7 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

Julien Y DutheilDepartment of Organismic Interactions, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany kahmann@mpi-marburg.mpg.de dutheil@evolbio.mpg.de.
Gertrud MannhauptDepartment of Organismic Interactions, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany German Research Center for Environmental Health (GmbH), Institute of Bioinformatics and Systems Biology, Helmholtz Zentrum München, Neuherberg, Germany.
Gabriel SchweizerDepartment of Organismic Interactions, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Christian M K SieberGerman Research Center for Environmental Health (GmbH), Institute of Bioinformatics and Systems Biology, Helmholtz Zentrum München, Neuherberg, Germany.
Martin MünsterkötterGerman Research Center for Environmental Health (GmbH), Institute of Bioinformatics and Systems Biology, Helmholtz Zentrum München, Neuherberg, Germany.
Ulrich GüldenerGerman Research Center for Environmental Health (GmbH), Institute of Bioinformatics and Systems Biology, Helmholtz Zentrum München, Neuherberg, Germany.
Jan SchirawskiDepartment of Organismic Interactions, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.
Regine KahmannDepartment of Organismic Interactions, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany kahmann@mpi-marburg.mpg.de dutheil@evolbio.mpg.de.
Institute of Bioinformatics and Systems Biology · DEMax Planck Institute for Terrestrial Microbiology · DEHelmholtz Zentrum München · DEInstitut des Sciences de l'Evolution de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Smut fungi are plant pathogens mostly parasitizing wild species of grasses as well as domesticated cereal crops. Genome analysis of several smut fungi including Ustilago maydis revealed a singular clustered organization of genes encoding secreted effectors. In U. maydis, many of these clusters have a role in virulence. Reconstructing the evolutionary history of clusters of effector genes is difficult because of their intrinsically fast evolution, which erodes the phylogenetic signal and homology relationships. Here, we describe the use of comparative evolutionary analyses of quality draft assemblies of genomes to study the mechanisms of this evolution. We report the genome sequence of a South African isolate of Sporisorium scitamineum, a smut fungus parasitizing sugar cane with a phylogenetic position intermediate to the two previously sequenced species U. maydis and Sporisorium reilianum. We show that the genome of S. scitamineum contains more and larger gene clusters encoding secreted effectors than any previously described species in this group. We trace back the origin of the clusters and find that their evolution is mainly driven by tandem gene duplication. In addition, transposable elements play a major role in the evolution of the clustered genes. Transposable elements are significantly associated with clusters of genes encoding fast evolving secreted effectors. This suggests that such clusters represent a case of genome compartmentalization that restrains the activity of transposable elements on genes under diversifying selection for which this activity is potentially beneficial, while protecting the rest of the genome from its deleterious effect.

Indexed as

Evolution, MolecularGenome, FungalDNA Transposable ElementsFungal ProteinsGene DuplicationGenomicsMultigene FamilyPhylogenyPlant DiseasesSaccharumUstilagoDNA Transposable ElementsFungal Proteinseffector proteinsgene clustergene duplicationgenome architecturerepeat sequencesselection interference

Identifiers

PMID26872771
PMCPMC4824034
OpenAlexW2305988912

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.