Evidence map›Paper›PMID 30111359›Full record

ArticleGenome biology2018

Evolutionarily conserved partial gene duplication in the Triticeae tribe of grasses confers pathogen resistance.

Jeyaraman Rajaraman, Dimitar Douchkov, Stefanie Lück, Götz Hensel, Daniela Nowara, Maria Pogoda, Twan Rutten, Tobias Meitzel, Jonathan Brassac, Caroline Höfle and 11 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Bioinformatics Analysis ofInternational journal of molecular sciences · 2023
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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

21 authors at 5 institutions in 2 countries.

Jeyaraman RajaramanLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany. rajaraman@ipk-gatersleben.de.ORCID 0000-0003-0946-0508
Dimitar DouchkovLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany. dushkov@ipk-gatersleben.de.
Stefanie LückLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Götz HenselLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Daniela NowaraLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Maria PogodaLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Twan RuttenLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Tobias MeitzelLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Jonathan BrassacLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Caroline HöfleTechnische Universität München, Emil-Ramann-Straße 2, D-85354, Freising, Germany.
Ralph HückelhovenTechnische Universität München, Emil-Ramann-Straße 2, D-85354, Freising, Germany.
Jörn KlinkenbergLeibniz Institut für Pflanzenbiochemie, Weinberg 3, D-06120, Halle (Saale), Germany.
Marco TrujilloLeibniz Institut für Pflanzenbiochemie, Weinberg 3, D-06120, Halle (Saale), Germany.
Eva BauerTechnische Universität München, Liesel-Beckmann-Straße 2, D-85354, Freising, Germany.
Thomas SchmutzerLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Axel HimmelbachLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Martin MascherLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Barbara LazzariParco Technologico Padano, Via Einstein, Loc. Cascina Codazza, 26900, Lodi, Italy.
Nils SteinLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Jochen KumlehnLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Patrick SchweizerLeibniz Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK Gatersleben), Corrensstrasse 3, D-06466, Stadt Seeland, Germany.
Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK) · DETechnical University of Munich · DELeibniz Institute of Plant Biochemistry · DEParco Tecnologico Padano · ITUniversity of Freiburg · DE

Funding

Bundesministerium für Bildung und Forschung GABI-nonhostBundesministerium für Bildung und Forschung GABI-phenomeDeutsche Forschungsgemeinschaft Schw 848/2-1FP7 Food, Agriculture and Fisheries, Biotechnology WHEALBISixth Framework Programme BIOEXPLOIT
6 · The paper itself

Abstract

backgroundThe large and highly repetitive genomes of the cultivated species Hordeum vulgare (barley), Triticum aestivum (wheat), and Secale cereale (rye) belonging to the Triticeae tribe of grasses appear to be particularly rich in gene-like sequences including partial duplicates. Most of them have been classified as putative pseudogenes. In this study we employ transient and stable gene silencing- and over-expression systems in barley to study the function of HvARM1 (for H. vulgare Armadillo 1), a partial gene duplicate of the U-box/armadillo-repeat E3 ligase HvPUB15 (for H. vulgare Plant U-Box 15).

resultsThe partial ARM1 gene is derived from a gene-duplication event in a common ancestor of the Triticeae and contributes to quantitative host as well as nonhost resistance to the biotrophic powdery mildew fungus Blumeria graminis. In barley, allelic variants of HvARM1 but not of HvPUB15 are significantly associated with levels of powdery mildew infection. Both HvPUB15 and HvARM1 proteins interact in yeast and plant cells with the susceptibility-related, plastid-localized barley homologs of THF1 (for Thylakoid formation 1) and of ClpS1 (for Clp-protease adaptor S1) of Arabidopsis thaliana. A genome-wide scan for partial gene duplicates reveals further events in barley resulting in stress-regulated, potentially neo-functionalized, genes.

conclusionThe results suggest neo-functionalization of the partial gene copy HvARM1 increases resistance against powdery mildew infection. It further links plastid function with susceptibility to biotrophic pathogen attack. These findings shed new light on a novel mechanism to employ partial duplication of protein-protein interaction domains to facilitate the expansion of immune signaling networks.

Indexed as

Evolution, MolecularGene DuplicationAllelesBase SequenceConserved SequenceDisease ResistanceGene Expression Regulation, PlantGene SilencingGenes, PlantGenetic MarkersHordeumHost-Pathogen InteractionsPlant DiseasesPlant ProteinsPlants, Genetically ModifiedPoaceaeGenetic MarkersPlant ProteinsDisease resistanceNeo-functionalizationPartial gene duplicationTriticeae grasses

Identifiers

PMID30111359
PMCPMC6092874
OpenAlexW2885951469

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.