Evidence map›Paper›PMID 31282048›Full record

ArticleMolecular ecology2019

Dynamic virulence-related regions of the plant pathogenic fungus Verticillium dahliae display enhanced sequence conservation.

Jasper R L Depotter, Xiaoqian Shi-Kunne, Hélène Missonnier, Tingli Liu, Luigi Faino, Grardy C M van den Berg, Thomas A Wood, Baolong Zhang, Alban Jacques, Michael F Seidl and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular ecology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 45 citations in OpenAlex.

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  18. Review
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  20. The Many Questions about Mini Chromosomes inPlants (Basel, Switzerland) · 2020
    Review
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

11 authors at 4 institutions in 4 countries.

Jasper R L DepotterLaboratory of Phytopathology, Wageningen University & Research, Wageningen, The Netherlands.
Xiaoqian Shi-KunneLaboratory of Phytopathology, Wageningen University & Research, Wageningen, The Netherlands.
Hélène MissonnierDépartement des Sciences Agronomiques et Agroalimentaires, Equipe Agrophysiologie et Agromolécules, Institut National Polytechnique de Toulouse - Ecole d'Ingénieurs de Purpan, Université de Toulouse, Toulouse, France.
Tingli LiuProvincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Luigi FainoLaboratory of Phytopathology, Wageningen University & Research, Wageningen, The Netherlands.
Grardy C M van den BergLaboratory of Phytopathology, Wageningen University & Research, Wageningen, The Netherlands.
Thomas A WoodDepartment of Crops and Agronomy, National Institute of Agricultural Botany, Cambridge, UK.
Baolong ZhangProvincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing, China.
Alban JacquesDépartement des Sciences Agronomiques et Agroalimentaires, Equipe Agrophysiologie et Agromolécules, Institut National Polytechnique de Toulouse - Ecole d'Ingénieurs de Purpan, Université de Toulouse, Toulouse, France.
Michael F SeidlLaboratory of Phytopathology, Wageningen University & Research, Wageningen, The Netherlands.
Bart P H J ThommaLaboratory of Phytopathology, Wageningen University & Research, Wageningen, The Netherlands.ORCID 0000-0003-4125-4181
Wageningen University & Research · NLJiangsu Academy of Agricultural Sciences · CNNational Institute of Agricultural Botany · GBUniversité Fédérale de Toulouse Midi-Pyrénées · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant pathogens continuously evolve to evade host immune responses. During host colonization, many fungal pathogens secrete effectors to perturb such responses, but these in turn may become recognized by host immune receptors. To facilitate the evolution of effector repertoires, such as the elimination of recognized effectors, effector genes often reside in genomic regions that display increased plasticity, a phenomenon that is captured in the two-speed genome hypothesis. The genome of the vascular wilt fungus Verticillium dahliae displays regions with extensive presence/absence polymorphisms, so-called lineage-specific regions, that are enriched in in planta-induced putative effector genes. As expected, comparative genomics reveals differential degrees of sequence divergence between lineage-specific regions and the core genome. Unanticipated, lineage-specific regions display markedly higher sequence conservation in coding as well as noncoding regions than the core genome. We provide evidence that disqualifies horizontal transfer to explain the observed sequence conservation and conclude that sequence divergence occurs at a slower pace in lineage-specific regions of the V. dahliae genome. We hypothesize that differences in chromatin organisation may explain lower nucleotide substitution rates in the plastic, lineage-specific regions of V. dahliae.

Indexed as

Genome, FungalBase SequenceConserved SequenceGene Transfer, HorizontalHaploidyModels, GeneticPhylogenyPlantsSelection, GeneticSpecies SpecificityVerticilliumVirulencecomparative genomicseffectorgenome evolutionmutagenesistwo-speed genomeVerticillium wilt

Identifiers

PMID31282048
PMCPMC6771948
OpenAlexW2960148605

What OpenQuestion holds

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Registered trials

None linked

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.