Evidence map›Paper›PMID 23231440›Full record

ArticleBMC genomics2012

Structure and evolution of barley powdery mildew effector candidates.

Carsten Pedersen, Emiel Ver Loren van Themaat, Liam J McGuffin, James C Abbott, Timothy A Burgis, Geraint Barton, Laurence V Bindschedler, Xunli Lu, Takaki Maekawa, Ralf Wessling and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed
20.5field-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

124 citing papers in PubMed, 260 citations in OpenAlex.

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  16. Powdery mildew effectors AVRMolecular plant pathology · 2024
    Article
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64 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

14 authors at 6 institutions in 3 countries.

Carsten PedersenDepartment of Agriculture & Ecology, Plant and Soil Science, University ofCopenhagen, Copenhagen, Denmark.
Emiel Ver Loren van Themaat
Liam J McGuffin
James C Abbott
Timothy A Burgis
Geraint Barton
Laurence V Bindschedler
Xunli Lu
Takaki Maekawa
Ralf Wessling
Rainer Cramer
Hans Thordal-Christensen
Ralph Panstruga
Pietro D Spanu
Imperial College London · GBMax Planck Institute for Plant Breeding Research · DEUniversity of Copenhagen · DKUniversity of Reading · GBRoyal Holloway University of London · GBRWTH Aachen University · DE

Funding

Biotechnology and Biological Sciences Research Council BB/H001646/1Biotechnology and Biological Sciences Research Council BB/H001948/1
6 · The paper itself

Abstract

backgroundProtein effectors of pathogenicity are instrumental in modulating host immunity and disease resistance. The powdery mildew pathogen of grasses Blumeria graminis causes one of the most important diseases of cereal crops. B. graminis is an obligate biotrophic pathogen and as such has an absolute requirement to suppress or avoid host immunity if it is to survive and cause disease.

resultsHere we characterise a superfamily predicted to be the full complement of Candidates for Secreted Effector Proteins (CSEPs) in the fungal barley powdery mildew parasite B. graminis f.sp. hordei. The 491 genes encoding these proteins constitute over 7% of this pathogen's annotated genes and most were grouped into 72 families of up to 59 members. They were predominantly expressed in the intracellular feeding structures called haustoria, and proteins specifically associated with the haustoria were identified by large-scale mass spectrometry-based proteomics. There are two major types of effector families: one comprises shorter proteins (100-150 amino acids), with a high relative expression level in the haustoria and evidence of extensive diversifying selection between paralogs; the second type consists of longer proteins (300-400 amino acids), with lower levels of differential expression and evidence of purifying selection between paralogs. An analysis of the predicted protein structures underscores their overall similarity to known fungal effectors, but also highlights unexpected structural affinities to ribonucleases throughout the entire effector super-family. Candidate effector genes belonging to the same family are loosely clustered in the genome and are associated with repetitive DNA derived from retro-transposons.

conclusionsWe employed the full complement of genomic, transcriptomic and proteomic analyses as well as structural prediction methods to identify and characterize the members of the CSEPs superfamily in B. graminis f.sp. hordei. Based on relative intron position and the distribution of CSEPs with a ribonuclease-like domain in the phylogenetic tree we hypothesize that the associated genes originated from an ancestral gene, encoding a secreted ribonuclease, duplicated successively by repetitive DNA-driven processes and diversified during the evolution of the grass and cereal powdery mildew lineage.

Indexed as

Amino Acid SequenceAscomycotaEdible GrainFungal ProteinsHordeumHost-Pathogen InteractionsMolecular Sequence DataMycosesPlant DiseasesProtein FoldingProtein Structure, TertiaryProteomicsSequence AlignmentFungal Proteins

Identifiers

PMID23231440
PMCPMC3582587
OpenAlexW2088989333

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.