Evidence map›Paper›PMID 28779550›Full record

ArticleMolecular plant pathology2018

The TNL gene Rdr1 confers broad-spectrum resistance to Diplocarpon rosae.

Ina Menz, Jannis Straube, Marcus Linde, Thomas Debener

Abstract read
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Article in Molecular plant pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

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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

16 citing papers in PubMed.

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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

4 authors.

Ina MenzDepartment of Molecular Plant Breeding, Institute for Plant Genetics, Leibniz Universität Hannover, Hannover 30419, Germany.
Jannis StraubeDepartment of Molecular Plant Breeding, Institute for Plant Genetics, Leibniz Universität Hannover, Hannover 30419, Germany.
Marcus LindeDepartment of Molecular Plant Breeding, Institute for Plant Genetics, Leibniz Universität Hannover, Hannover 30419, Germany.
Thomas DebenerDepartment of Molecular Plant Breeding, Institute for Plant Genetics, Leibniz Universität Hannover, Hannover 30419, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Black spot disease, which is caused by the ascomycete Diplocarpon rosae, is the most severe disease in field-grown roses in temperate regions and has been distributed worldwide, probably together with commercial cultivars. Here, we present data indicating that muRdr1A is the active Rdr1 gene, a single-dominant TIR-NBS-LRR (Toll/interleukin-1 receptor-nucleotide binding site-leucine rich repeat) (TNL)-type resistance gene against black spot disease, which acts against a broad range of pathogenic isolates independent of the genetic background of the host genotype. Molecular analyses revealed that, compared with the original donor genotype, the multiple integrations that are found in the primary transgenic clone segregate into different integration patterns in its sexual progeny and do not show any sign of overexpression. Rdr1 provides resistance to 13 different single-spore isolates belonging to six different races and broad field mixtures of conidia; thus far, Rdr1 is only overcome by two races. The expression of muRdr1A, the active Rdr1 gene, leads to interaction patterns that are identical in the transgenic clones and the non-transgenic original donor genotype. This finding indicates that the interacting avirulence (Avr) factor on the pathogen side must be widespread among the pathogen populations and may have a central function in the rose-black spot interaction. Therefore, the Rdr1 gene, pyramided with only a few other R genes by sexual crosses, might be useful for breeding roses that are resistant to black spot because the spread of new pathogenic races of the fungus appears to be slow.

Indexed as

Genes, PlantAscomycotaDisease ResistanceGene Expression Regulation, PlantGenetic Complementation TestGenotypePlant DiseasesPlant ProteinsPlants, Genetically ModifiedRosaSpores, FungalPlant Proteinsblack spotdisease resistanceeffector-triggered immunityNBS-LRRplant immunityR generoses

Identifiers

PMID28779550
PMCPMC6638031

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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.