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The dispensable chromosome of L eptosphaeria maculans shelters an effector gene conferring avirulence towards B rassica rapa

https://doi.org/10.1111/nph.12178
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/1-4020-4525-5_2openalex-snapshot
Genetic linkage maps and genomic organization in Leptosphaeria maculans
inferredcites →https://doi.org/10.1007/1-4020-4525-5_5openalex-snapshot
A large-scale survey of races of Leptosphaeria maculans occurring on oilseed rape in France
inferredcites →https://doi.org/10.1007/bf00293142openalex-snapshot
Inheritance of chromosomal length polymorphisms in the ascomycete Leptosphaeria maculans
inferredcites →https://doi.org/10.1007/bf00324673openalex-snapshot
Major chromosomal length polymorphisms are evident after meiosis in the phytopathogenic fungus Leptosphaeria maculans
inferredcites →https://doi.org/10.1007/s00122-006-0393-0openalex-snapshot
Pairing and recombination at meiosis of Brassica rapa (AA) × Brassica napus (AACC) hybrids
inferredcites →https://doi.org/10.1007/s00122-007-0616-zopenalex-snapshot
Detection, introgression and localization of genes conferring specific resistance to Leptosphaeria maculans from Brassica rapa into B. napus
inferredcites →https://doi.org/10.1007/s00294-003-0390-7openalex-snapshot
Meiotic behavior of a supernumerary chromosome in Magnaporthe oryzae
inferredcites →https://doi.org/10.1007/s00294-003-0391-6openalex-snapshot
Characterisation of the mating-type locus of the plant pathogenic ascomycete Leptosphaeria maculans
inferredcites →https://doi.org/10.1007/s00294-004-0539-zopenalex-snapshot
Identification and characterization of polymorphic minisatellites in the phytopathogenic ascomycete Leptosphaeria maculans
inferredcites →https://doi.org/10.1007/s002940050167openalex-snapshot
Meiotic behaviour of the minichromosome in the phytopathogenic ascomycete Leptosphaeria maculans
inferredcites →https://doi.org/10.1007/s002940050342openalex-snapshot
Supernumerary chromosomes in filamentous fungi
inferredcites →https://doi.org/10.1007/s002940100233openalex-snapshot
Spontaneous loss of a conditionally dispensable chromosome from the Alternaria alternata apple pathotype leads to loss of toxin production and pathogenicity
inferredcites →https://doi.org/10.1007/s10658-005-2104-0openalex-snapshot
A Large-Scale Survey of Races of Leptosphaeria maculans Occurring on Oilseed Rape in France
inferredcites →https://doi.org/10.1007/s10658-005-2643-4openalex-snapshot
Fitness Cost Associated with Loss of the AvrLm4 Avirulence Function in Leptosphaeria maculans (Phoma Stem Canker of Oilseed Rape)
inferredcites →https://doi.org/10.1007/s10658-005-2931-zopenalex-snapshot
Frequency of Avirulence Alleles in Field Populations of Leptosphaeria maculans in Europe
inferredcites →https://doi.org/10.1007/s10658-005-3168-6openalex-snapshot
Genetic Linkage Maps and Genomic Organization in Leptosphaeria maculans
inferredcites →https://doi.org/10.1016/j.tig.2004.07.007openalex-snapshot
RIP: the evolutionary cost of genome defense
inferredcites →https://doi.org/10.1016/s1087-1845(02)00588-1openalex-snapshot
Analysis of loss of pathogenicity mutants reveals that repeat-induced point mutations can occur in the Dothideomycete Leptosphaeria maculans
inferredcites →https://doi.org/10.1023/a:1025597622490openalex-snapshot
Screening and identification of resistance to Leptosphaeria maculans (stem canker) in Brassica napus accessions
inferredcites →https://doi.org/10.1038/nature08850openalex-snapshot
Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium
inferredcites →https://doi.org/10.1038/ncomms1189openalex-snapshot
Effector diversification within compartments of the Leptosphaeria maculans genome affected by Repeat-Induced Point mutations
inferredcites →https://doi.org/10.1093/genetics/130.1.81openalex-snapshot
A restriction fragment length polymorphism map and electrophoretic karyotype of the fungal maize pathogen Cochliobolus heterostrophus.
inferredcites →https://doi.org/10.1093/genetics/161.1.59openalex-snapshot
A Conditionally Dispensable Chromosome Controls Host-Specific Pathogenicity in the Fungal Plant Pathogen Alternaria alternata
inferredcites →https://doi.org/10.1094/mpmi-20-4-0459openalex-snapshot
Heterochromatin-Like Regions as Ecological Niches for Avirulence Genes in the Leptosphaeria maculans Genome: Map-Based Cloning of AvrLm6
inferredcites →https://doi.org/10.1094/mpmi-22-8-0932openalex-snapshot
Repeat-Induced Point Mutation (RIP) as an Alternative Mechanism of Evolution Toward Virulence in Leptosphaeria maculans
inferredcites →https://doi.org/10.1094/phyto-84-1299openalex-snapshot
Tetrad Analysis of Acid Phosphatase, Soluble Protein Patterns, and Mating Type inLeptosphaeria maculans
inferredcites →https://doi.org/10.1094/phyto-85-1525openalex-snapshot
Genetic Characterization ofAvrLm1,the First Avirulence Gene ofLeptosphaeria maculans
inferredcites →https://doi.org/10.1094/phyto-95-1061openalex-snapshot
Analysis of Leptosphaeria maculans Race Structure in a Worldwide Collection of Isolates
inferredcites →https://doi.org/10.1094/phyto.2001.91.1.70openalex-snapshot
Genetic Control and Host Range of Avirulence Toward Brassica napus Cultivars Quinta and Jet Neuf in Leptosphaeria maculans
inferredcites →https://doi.org/10.1094/phyto.2002.92.10.1122openalex-snapshot
New Avirulence Genes in the Phytopathogenic Fungus Leptosphaeria maculans
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05076.xopenalex-snapshot
Lost in the middle of nowhere: the AvrLm1 avirulence gene of the Dothideomycete Leptosphaeria maculans
inferredcites →https://doi.org/10.1111/j.1365-2958.2008.06547.xopenalex-snapshot
Leptosphaeria maculans avirulence gene AvrLm4‐7 confers a dual recognition specificity by the Rlm4 and Rlm7 resistance genes of oilseed rape, and circumvents Rlm4‐mediated recognition through a single amino acid change
inferredcites →https://doi.org/10.1111/j.1365-3059.2008.01982.xopenalex-snapshot
Dual control of avirulence in Leptosphaeria maculans towards a Brassica napus cultivar with ‘ sylvestris ‐derived’ resistance suggests involvement of two resistance genes
inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01408.xopenalex-snapshot
Genome structure impacts molecular evolution at the AvrLm1 avirulence locus of the plant pathogen Leptosphaeria maculans
inferredcites →https://doi.org/10.1111/j.1469-8137.1995.tb03079.xopenalex-snapshot
B chromosomes in plants
inferredcites →https://doi.org/10.1111/j.1574-6976.2010.00263.xopenalex-snapshot
Horizontal gene and chromosome transfer in plant pathogenic fungi affecting host range
inferredcites →https://doi.org/10.1128/aem.72.1.185-191.2006openalex-snapshot
Genetic Variability and Distribution of Mating Type Alleles in Field Populations of Leptosphaeria maculans from France
inferredcites →https://doi.org/10.1186/1471-2164-13-171openalex-snapshot
Genomic characterization of the conditionally dispensable chromosome in Alternaria arborescens provides evidence for horizontal gene transfer
inferredcites →https://doi.org/10.1186/1756-0500-3-322openalex-snapshot
FONZIE: An optimized pipeline for minisatellite marker discovery and primer design from large sequence data sets
inferredcites →https://doi.org/10.1371/journal.pgen.1000618openalex-snapshot
The Genome of Nectria haematococca: Contribution of Supernumerary Chromosomes to Gene Expansion
inferredcites →https://doi.org/10.1371/journal.pgen.1002070openalex-snapshot
Finished Genome of the Fungal Wheat Pathogen Mycosphaerella graminicola Reveals Dispensome Structure, Chromosome Plasticity, and Stealth Pathogenesis
inferredcites →https://doi.org/10.1371/journal.pone.0005863openalex-snapshot
Meiosis Drives Extraordinary Genome Plasticity in the Haploid Fungal Plant Pathogen Mycosphaerella graminicola
inferredcites →https://doi.org/10.1371/journal.ppat.1002147openalex-snapshot
Multiple Translocation of the AVR-Pita Effector Gene among Chromosomes of the Rice Blast Fungus Magnaporthe oryzae and Related Species
inferredcites →https://doi.org/10.1371/journal.ppat.1003020openalex-snapshot
Genome Structure and Reproductive Behaviour Influence the Evolutionary Potential of a Fungal Phytopathogen
inferredcites →https://doi.org/10.1534/genetics.110.122713openalex-snapshot
A Single, Recent Origin of the Accessory B Chromosome of the Grasshopper Eyprepocnemis plorans

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4781016openalex-extracted
Slipping Through the Cracks: Challenges and Prospects for Managing Fungal Pathogens Involved in Plant Disease Complexes
inferred← citeshttps://doi.org/10.1002/ps.7401openalex-snapshot
Large‐scale population survey of Leptosphaeria maculans in France highlights both on‐going breakdowns and potentially effective resistance genes in oilseed rape
inferred← citeshttps://doi.org/10.1007/978-3-030-49924-2_2openalex-snapshot
2 Origin, Function, and Transmission of Accessory Chromosomes
inferred← citeshttps://doi.org/10.1007/978-3-030-91035-8_5openalex-snapshot
Genomic Designing for Biotic Stress Resistance in Rape and Mustard
inferred← citeshttps://doi.org/10.1007/978-3-031-16503-0openalex-snapshot
Plant Relationships
inferred← citeshttps://doi.org/10.1007/978-3-031-16503-0_11openalex-snapshot
Epigenetic Regulation of Fungal Genes Involved in Plant Colonization
inferred← citeshttps://doi.org/10.1007/978-3-319-10503-1_4openalex-snapshot
Repeat-Induced Point Mutation: A Fungal-Specific, Endogenous Mutagenesis Process
inferred← citeshttps://doi.org/10.1007/978-3-319-43694-4_13openalex-snapshot
Case Study for Trait-Related Gene Evolution: Disease Resistance Genes in Brassica napus
inferred← citeshttps://doi.org/10.1007/978-3-319-43694-4_3openalex-snapshot
Genes and Quantitative Trait Loci Mapping for Major Agronomic Traits in Brassica napus L.
inferred← citeshttps://doi.org/10.1007/978-981-16-0862-9_2openalex-snapshot
Identification of R-Genes Sources
inferred← citeshttps://doi.org/10.1007/978-981-16-1974-8_3openalex-snapshot
Molecular Mechanisms of Host Resistance to Hemibiotrophs and Necrotrophs
inferred← citeshttps://doi.org/10.1007/978-981-19-3812-2_4openalex-snapshot
Molecular Detection and Identification of Pathogens, Pathotypes, and Genes
inferred← citeshttps://doi.org/10.1007/978-981-19-3812-2_5openalex-snapshot
Pathogenomics of Pathogenic Variability
inferred← citeshttps://doi.org/10.1007/bf03356546openalex-snapshot
Pathogenic Variability and Prevalence of Avr Genes in Leptosphaeria maculans Populations from Alberta, Canada
inferred← citeshttps://doi.org/10.1007/s00122-014-2298-7openalex-snapshot
Molecular cytogenetic identification of B genome chromosomes linked to blackleg disease resistance in Brassica napus × B. carinata interspecific hybrids
inferred← citeshttps://doi.org/10.1007/s00122-018-3103-9openalex-snapshot
Multi-year linkage and association mapping confirm the high number of genomic regions involved in oilseed rape quantitative resistance to blackleg
inferred← citeshttps://doi.org/10.1007/s00122-024-04641-wopenalex-snapshot
Breeding and management of major resistance genes to stem canker/blackleg in Brassica crops
inferred← citeshttps://doi.org/10.1007/s10142-013-0324-5openalex-snapshot
Identifying genetic diversity of avirulence genes in Leptosphaeria maculans using whole genome sequencing
inferred← citeshttps://doi.org/10.1007/s10577-021-09658-1openalex-snapshot
Genome-wide mapping of histone modifications during axenic growth in two species of Leptosphaeria maculans showing contrasting genomic organization
inferred← citeshttps://doi.org/10.1007/s10577-022-09691-8openalex-snapshot
Non-Mendelian transmission of accessory chromosomes in fungi
inferred← citeshttps://doi.org/10.1007/s10658-015-0819-0openalex-snapshot
Breakdown of Rlm3 resistance in the Brassica napus–Leptosphaeria maculans pathosystem in western Canada
inferred← citeshttps://doi.org/10.1007/s10658-015-0827-0openalex-snapshot
Infection of canola pods by Leptosphaeria maculans and subsequent seed contamination
inferred← citeshttps://doi.org/10.1007/s10658-016-0932-8openalex-snapshot
Race spectra of Leptosphaeria maculans, the causal agent of blackleg disease of oilseed rape, in different geographic regions in northern Germany
inferred← citeshttps://doi.org/10.1007/s10658-017-1210-0openalex-snapshot
Korean Brassica oleracea germplasm offers a novel source of qualitative resistance to blackleg disease
inferred← citeshttps://doi.org/10.1007/s10658-018-1465-0openalex-snapshot
Rapid detection of Leptosphaeria maculans avirulence gene AvrLm4-7 conferring the avirulence/virulence specificity on Brassica napus using a tetra-primer ARMS-PCR
inferred← citeshttps://doi.org/10.1007/s10658-020-01963-5openalex-snapshot
Virulence/avirulence patterns among Leptosphaeria maculans isolates determines expression of resistance, senescence and yellowing in cotyledons of Brassica napus
inferred← citeshttps://doi.org/10.1007/s10658-021-02354-0openalex-snapshot
Identification of genomic regions associated with resistance to blackleg (Leptosphaeria maculans) in canola using genome wide association study
inferred← citeshttps://doi.org/10.1007/s10658-022-02498-7openalex-snapshot
Comparing the effectiveness of R genes in a 2-year canola–wheat rotation against Leptosphaeria maculans, the causal agent of blackleg disease in Brassica species
inferred← citeshttps://doi.org/10.1007/s11032-015-0356-8openalex-snapshot
Connected populations for detecting quantitative resistance factors to phoma stem canker in oilseed rape (Brassica napus L.)
inferred← citeshttps://doi.org/10.1007/s11032-026-01690-5openalex-snapshot
Segregating BC2F1 interspecific hybrids between Brassica napus and B. nigra reveal a major effect locus for blackleg resistance on chromosome B2
inferred← citeshttps://doi.org/10.1007/s11033-020-05779-8openalex-snapshot
Development of a specific marker for detection of a functional AvrLm9 allele and validating the interaction between AvrLm7 and AvrLm9 in Leptosphaeria maculans
inferred← citeshttps://doi.org/10.1007/s13313-014-0337-0openalex-snapshot
Incidence and severity of blackleg caused by Leptosphaeria spp. in juncea canola (Brassica juncea L.) in Australia
inferred← citeshttps://doi.org/10.1007/s13313-020-00767-9openalex-snapshot
Epidemiology and management of blackleg of canola in response to changing farming practices in Australia
inferred← citeshttps://doi.org/10.1007/s13353-014-0235-8openalex-snapshot
Molecular screening for avirulence alleles AvrLm1 and AvrLm6 in airborne inoculum of Leptosphaeria maculans and winter oilseed rape (Brassica napus) plants from Poland and the UK
inferred← citeshttps://doi.org/10.1016/b978-0-12-397940-7.00003-3openalex-snapshot
Evolutionary and Adaptive Role of Transposable Elements in Fungal Genomes
inferred← citeshttps://doi.org/10.1016/bs.abr.2016.09.003openalex-snapshot
Effector-Mediated Communication of Filamentous Plant Pathogens With Their Hosts
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116062openalex-snapshot
The Fusarium verticillioides minichromosome negatively regulates the biosynthesis of carcinogenic fumonisins during maize infection
inferred← citeshttps://doi.org/10.1016/j.cropro.2024.106697openalex-snapshot
Identification of new lines resistance to blackleg in an Argentinian rapeseed-breeding program
inferred← citeshttps://doi.org/10.1016/j.cropro.2024.106826openalex-snapshot
Slipping through the cracks: Challenges and prospects for investigating fungal plant disease complexes
inferred← citeshttps://doi.org/10.1016/j.fbr.2021.09.002openalex-snapshot
Next-generation sequencing provides important insights into the biology and evolution of the Botryosphaeriaceae
inferred← citeshttps://doi.org/10.1016/j.fcr.2014.06.023openalex-snapshot
Breakdown of resistance to the fungal disease, blackleg, is averted in commercial canola (Brassica napus) crops in Australia
inferred← citeshttps://doi.org/10.1016/j.fgb.2015.08.010openalex-snapshot
Mind the gap; seven reasons to close fragmented genome assemblies
inferred← citeshttps://doi.org/10.1016/j.fgb.2016.12.008openalex-snapshot
Impact of biotic and abiotic factors on the expression of fungal effector-encoding genes in axenic growth conditions
inferred← citeshttps://doi.org/10.1016/j.fgb.2019.103320openalex-snapshot
LmCBP1, a secreted chitin-binding protein, is required for the pathogenicity of Leptosphaeria maculans on Brassica napus
inferred← citeshttps://doi.org/10.1016/j.fgb.2020.103447openalex-snapshot
Host-specificity factors in plant pathogenic fungi
inferred← citeshttps://doi.org/10.1016/j.jgg.2021.06.019openalex-snapshot
Genetic diversity and population structure of Leptosphaeria maculans isolates in Western Canada
inferred← citeshttps://doi.org/10.1016/j.mib.2018.01.012openalex-snapshot
To B or not to B: a tale of unorthodox chromosomes
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.05.025openalex-snapshot
Chromatin-based control of effector gene expression in plant-associated fungi
inferred← citeshttps://doi.org/10.1016/j.tplants.2014.04.009openalex-snapshot
Effector-triggered defence against apoplastic fungal pathogens
inferred← citeshttps://doi.org/10.1038/s41467-021-26108-yopenalex-snapshot
Epigenetic modifications affect the rate of spontaneous mutations in a pathogenic fungus
inferred← citeshttps://doi.org/10.1038/s41598-019-43419-9openalex-snapshot
Dissecting R gene and host genetic background effect on the Brassica napus defense response to Leptosphaeria maculans
inferred← citeshttps://doi.org/10.1051/ocl/2014043openalex-snapshot
Research fields, challenges and opportunities in European oilseed crops breeding
inferred← citeshttps://doi.org/10.1071/cp15221openalex-snapshot
Blackleg disease of canola in Australia
inferred← citeshttps://doi.org/10.1071/cp16411openalex-snapshot
Changes in allele frequencies of avirulence genes in the blackleg fungus, Leptosphaeria maculans, over two decades in Australia
inferred← citeshttps://doi.org/10.1079/9781789247848.0002openalex-snapshot
The Impact of Genomics in Identifying Blackleg Disease Resistance Genes in Canola
inferred← citeshttps://doi.org/10.1080/07060661.2019.1643788openalex-snapshot
Advances in understanding the Leptosphaeria maculans - Brassica pathosystem and their impact on disease management
inferred← citeshttps://doi.org/10.1080/07060661.2021.1991480openalex-snapshot
Sustainability on the farm: breeding for resistance and management of major canola diseases in Canada contributing towards an IPM approach
inferred← citeshttps://doi.org/10.1093/g3journal/jkad214openalex-snapshot
Population genomic analyses suggest recent dispersal events of the pathogen Cercospora zeina into East and Southern African maize cropping systems
inferred← citeshttps://doi.org/10.1093/molbev/msae164openalex-snapshot
Multiple Horizontal Mini-chromosome Transfers Drive Genome Evolution of Clonal Blast Fungus Lineages
inferred← citeshttps://doi.org/10.1094/mpmi-05-19-0128-ropenalex-snapshot
A Comparative Genomic Analysis of the Barley Pathogen Pyrenophora teres f. teres Identifies Subtelomeric Regions as Drivers of Virulence
inferred← citeshttps://doi.org/10.1094/mpmi-06-17-0135-fiopenalex-snapshot
Accessories Make the Outfit: Accessory Chromosomes and Other Dispensable DNA Regions in Plant-Pathogenic Fungi
inferred← citeshttps://doi.org/10.1094/mpmi-08-24-0082-taopenalex-snapshot
ZymoSoups: A High-Throughput Forward Genetics Method for Rapid Identification of Virulence Genes in Zymoseptoria tritici
inferred← citeshttps://doi.org/10.1094/pbiomes-07-23-0069-ropenalex-snapshot
A Specific Resistance Gene to Leptosphaeria maculans, Rlm11, Has a Limited Impact on Brassica napus Mycobiota Compared with Plant Compartment or Cropping Season Effects
inferred← citeshttps://doi.org/10.1094/pdis-01-19-0181-reopenalex-snapshot
Characterization of the Race Structure of Leptosphaeria maculans Causing Blackleg of Winter Canola in Oklahoma and Kansas
inferred← citeshttps://doi.org/10.1094/pdis-05-17-0630-reopenalex-snapshot
A Six-Year Investigation of the Dynamics of Avirulence Allele Profiles, Blackleg Incidence, and Mating Type Alleles ofLeptosphaeria maculansPopulations Associated with Canola Crops in Manitoba, Canada
inferred← citeshttps://doi.org/10.1094/pdis-08-20-1838-reopenalex-snapshot
Leptosphaeria maculans Isolates Reveal Their Allele Frequency in Western Canada
inferred← citeshttps://doi.org/10.1094/phyto-02-16-0110-fiopenalex-snapshot
The Age of Effectors: Genome-Based Discovery and Applications
inferred← citeshttps://doi.org/10.1094/phyto-04-24-0129-ropenalex-snapshot
A New Threat to Limber Pine ( Pinus flexilis ) Restoration in Alberta and Beyond: First Documentation of a Cronartium ribicola Race ( vcr4 ) Virulent to Cr4- Controlled Major Gene Resistance
inferred← citeshttps://doi.org/10.1094/phyto-12-22-0466-ropenalex-snapshot
Polymorphism of Avirulence Genes and Adaptation to Brassica Resistance Genes Is Gene-Dependent in the Phytopathogenic Fungus Leptosphaeria maculans
inferred← citeshttps://doi.org/10.1099/mgen.0.000637openalex-snapshot
Remote homology clustering identifies lowly conserved families of effector proteins in plant-pathogenic fungi
inferred← citeshttps://doi.org/10.1099/mgen.0.000819openalex-snapshot
A chromosome-scale genome assembly of the tomato pathogen Cladosporium fulvum reveals a compartmentalized genome architecture and the presence of a dispensable chromosome
inferred← citeshttps://doi.org/10.1101/2020.01.09.900167openalex-snapshot
A Leptosphaeria maculans set of isolates characterised on all available differentials and used as control to identify virulence frequencies in a current French population
inferred← citeshttps://doi.org/10.1101/2020.05.20.106880openalex-snapshot
A large accessory genome, high recombination rates, and selection of secondary metabolite genes help maintain global distribution and broad host range of the fungal plant pathogen Claviceps purpurea
inferred← citeshttps://doi.org/10.1101/2021.12.15.472773openalex-snapshot
Regulation of effector gene expression as concerted waves in Leptosphaeria maculans : a two-players game
inferred← citeshttps://doi.org/10.1101/2022.05.10.491286openalex-snapshot
The neighboring genes AvrLm10A and AvrLm10B are part of a large multigene family of cooperating effector genes conserved in Dothideomycetes and Sordariomycetes
inferred← citeshttps://doi.org/10.1101/2024.02.13.580079openalex-snapshot
Multiple horizontal mini-chromosome transfers drive genome evolution of clonal blast fungus lineages
inferred← citeshttps://doi.org/10.1101/2024.10.03.616481openalex-snapshot
Interspecies hybridization as a route of accessory chromosome origin in fungal species infecting wild grasses
inferred← citeshttps://doi.org/10.1101/229997openalex-snapshot
Extremely flexible infection programs in a fungal plant pathogen
inferred← citeshttps://doi.org/10.1111/aab.12112openalex-snapshot
Use of high resolution melting analysis to genotype the avirulence AvrLm4 ‐7 gene of Leptosphaeria maculans, a fungal pathogen of Brassica napus
inferred← citeshttps://doi.org/10.1111/mec.14046openalex-snapshot
Unusual evolutionary mechanisms to escape effector‐triggered immunity in the fungal phytopathogen Leptosphaeria maculans
inferred← citeshttps://doi.org/10.1111/mec.70105openalex-snapshot
Adaptation of the Cyst Nematode Globodera pallida to the Colinear Potato Resistant QTLs GpaV vrn and GpaV spl Involved Distinct Genomic Regions and Absence of Cross‐Virulence
inferred← citeshttps://doi.org/10.1111/mpp.12105openalex-snapshot
An avirulence gene, AvrLmJ1 , from the blackleg fungus, L eptosphaeria maculans , confers avirulence to B rassica juncea cultivars
inferred← citeshttps://doi.org/10.1111/mpp.12228openalex-snapshot
Rapid identification of the L eptosphaeria maculans avirulence gene AvrLm2 using an intraspecific comparative genomics approach
inferred← citeshttps://doi.org/10.1111/mpp.12249openalex-snapshot
The APSES transcription factor LmStuA is required for sporulation, pathogenic development and effector gene expression in L eptosphaeria maculans
inferred← citeshttps://doi.org/10.1111/mpp.12251openalex-snapshot
Effector discovery in the fungal wheat pathogen Z ymoseptoria tritici
inferred← citeshttps://doi.org/10.1111/mpp.12332openalex-snapshot
L eptosphaeria maculans effector AvrLm4‐7 affects salicylic acid (SA) and ethylene (ET) signalling and hydrogen peroxide (H 2 O 2 ) accumulation in B rassica napus
inferred← citeshttps://doi.org/10.1111/mpp.12356openalex-snapshot
Genome‐wide transcriptomic analyses provide insights into the lifestyle transition and effector repertoire of Leptosphaeria maculans during the colonization of Brassica napus seedlings
inferred← citeshttps://doi.org/10.1111/mpp.12440openalex-snapshot
Dispensable chromosomes in Fusarium oxysporum f. sp. lycopersici
inferred← citeshttps://doi.org/10.1111/mpp.12464openalex-snapshot
Different waves of effector genes with contrasted genomic location are expressed by Leptosphaeria maculans during cotyledon and stem colonization of oilseed rape
inferred← citeshttps://doi.org/10.1111/mpp.12574openalex-snapshot
One gene‐one name: the AvrLmJ1 avirulence gene of Leptosphaeria maculans is AvrLm5
inferred← citeshttps://doi.org/10.1111/mpp.12658openalex-snapshot
Leptosphaeria maculans AvrLm9: a new player in the game of hide and seek with AvrLm4‐7
inferred← citeshttps://doi.org/10.1111/mpp.12994openalex-snapshot
Impact of a resistance gene against a fungal pathogen on the plant host residue microbiome: The case of the Leptosphaeria maculans–Brassica napus pathosystem
inferred← citeshttps://doi.org/10.1111/mpp.13131openalex-snapshot
A new avirulence gene of Leptosphaeria maculans, AvrLm14, identifies a resistance source in American broccoli (Brassica oleracea) genotypes
inferred← citeshttps://doi.org/10.1111/mpp.13194openalex-snapshot
Two independent approaches converge to the cloning of a new Leptosphaeria maculans avirulence effector gene, AvrLmS‐Lep2
inferred← citeshttps://doi.org/10.1111/mpp.13204openalex-snapshot
Independent breakdown events of the Brassica napus Rlm7 resistance gene including via the off‐target impact of a dual‐specificity avirulence interaction
inferred← citeshttps://doi.org/10.1111/mpp.13338openalex-snapshot
The neighbouring genes AvrLm10A and AvrLm10B are part of a large multigene family of cooperating effector genes conserved in Dothideomycetes and Sordariomycetes
inferred← citeshttps://doi.org/10.1111/nph.12804openalex-snapshot
Introduction to a V irtual S pecial I ssue on phytopathogen effector proteins
inferred← citeshttps://doi.org/10.1111/nph.13736openalex-snapshot
A game of hide and seek between avirulence genes AvrLm4‐7 and AvrLm3 in Leptosphaeria maculans
inferred← citeshttps://doi.org/10.1111/nph.14411openalex-snapshot
Life, death and rebirth of avirulence effectors in a fungal pathogen of B rassica crops, L eptosphaeria maculans
inferred← citeshttps://doi.org/10.1111/nph.15762openalex-snapshot
A two genes – for – one gene interaction between Leptosphaeria maculans and Brassica napus
inferred← citeshttps://doi.org/10.1111/nph.16092openalex-snapshot
An evolutionary framework for host shifts – jumping ships for survival
inferred← citeshttps://doi.org/10.1111/nph.19581openalex-snapshot
Regulation of effector gene expression as concerted waves in Leptosphaeria maculans: a two‐player game
inferred← citeshttps://doi.org/10.1111/pbi.12341openalex-snapshot
The B rassica napus receptor‐like protein RLM 2 is encoded by a second allele of the L ep R 3/ R lm2 blackleg resistance locus
inferred← citeshttps://doi.org/10.1111/pbr.12343openalex-snapshot
Gene‐for‐gene resistance is expressed in cotyledons, leaves and pods, but not during late stages of stem colonization in the Leptosphaeria maculans–Brassica napus pathosystem
inferred← citeshttps://doi.org/10.1111/pbr.12587openalex-snapshot
Development of molecular markers linked to the Leptosphaeria maculans resistance gene Rlm6 and inheritance of SCAR and CAPS markers in Brassica napus × Brassica juncea interspecific hybrids
inferred← citeshttps://doi.org/10.1111/ppa.12479openalex-snapshot
Cytogenomic characterization of Colletotrichum kahawae , the causal agent of coffee berry disease, reveals diversity in minichromosome profiles and genome size expansion
inferred← citeshttps://doi.org/10.1111/ppa.12489openalex-snapshot
Race structure and frequency of avirulence genes in the western Canadian Leptosphaeria maculans pathogen population, the causal agent of blackleg in brassica species
inferred← citeshttps://doi.org/10.1111/ppa.12626openalex-snapshot
Identifying seedling and adult plant resistance of Chinese Brassica napus germplasm to Leptosphaeria maculans
inferred← citeshttps://doi.org/10.1111/ppa.13293openalex-snapshot
Impact of Brassica napus–Leptosphaeria maculans interaction on the emergence of virulent isolates of L. maculans , causal agent of blackleg disease in canola
inferred← citeshttps://doi.org/10.1111/ppa.13323openalex-snapshot
New specific quantitative real‐time PCR assays shed light on the epidemiology of two species of the Leptosphaeria maculans – Leptosphaeria biglobosa species complex
inferred← citeshttps://doi.org/10.1111/ppa.13801openalex-snapshot
A new set of international Leptosphaeria maculans isolates as a resource for elucidation of the basis and evolution of blackleg disease on Brassica napus
inferred← citeshttps://doi.org/10.1111/ppa.13958openalex-snapshot
Frequency of avirulence genes and race structure in a Leptosphaeria maculans population in Tunisia
inferred← citeshttps://doi.org/10.1111/ppa.14018openalex-snapshot
Strategic genetic insights and integrated approaches for successful management of blackleg in canola/rapeseed farming
inferred← citeshttps://doi.org/10.1111/ppa.70063openalex-snapshot
Molecular Investigation of Rlm3 From Rapeseed as a Potential Broad‐Spectrum Resistance Gene Against Fungal Pathogens Producing Structurally Conserved Effectors
inferred← citeshttps://doi.org/10.1111/ppa.70078openalex-snapshot
Introgression of Resistance Against Leptosphaeria maculans From Brassica juncea Into Brassica napus
inferred← citeshttps://doi.org/10.1111/tpj.12913openalex-snapshot
Crystal structure of the effector A vr L m4–7 of Leptosphaeria maculans reveals insights into its translocation into plant cells and recognition by resistance proteins
inferred← citeshttps://doi.org/10.1128/9781555819583.ch29openalex-snapshot
Fungal Genomes and Insights into the Evolution of the Kingdom
inferred← citeshttps://doi.org/10.1128/ec.00084-15openalex-snapshot
A Novel Type Pathway-Specific Regulator and Dynamic Genome Environments of a Solanapyrone Biosynthesis Gene Cluster in the Fungus Ascochyta rabiei
inferred← citeshttps://doi.org/10.1128/mbio.03468-25openalex-snapshot
Interspecies hybridization as a route of accessory chromosome origin in fungal pathogens
inferred← citeshttps://doi.org/10.1128/microbiolspec.funk-0055-2016openalex-snapshot
Fungal Genomes and Insights into the Evolution of the Kingdom
inferred← citeshttps://doi.org/10.1128/msphere.00128-20openalex-snapshot
An Avirulence Gene Cluster in the Wheat Stripe Rust Pathogen (Puccinia striiformis f. sp. tritici ) Identified through Genetic Mapping and Whole-Genome Sequencing of a Sexual Population
inferred← citeshttps://doi.org/10.1146/annurev-phyto-021621-120602openalex-snapshot
Molecular Interactions Between Leptosphaeria maculans and Brassica Species
inferred← citeshttps://doi.org/10.1146/annurev-phyto-080615-095928openalex-snapshot
Karyotype Variability in Plant-Pathogenic Fungi
inferred← citeshttps://doi.org/10.1186/1471-2164-15-891openalex-snapshot
Transposable element-assisted evolution and adaptation to host plant within the Leptosphaeria maculans-Leptosphaeria biglobosa species complex of fungal pathogens
inferred← citeshttps://doi.org/10.1186/s12864-016-2486-8openalex-snapshot
Comparative genomics and prediction of conditionally dispensable sequences in legume–infecting Fusarium oxysporum formae speciales facilitates identification of candidate effectors
inferred← citeshttps://doi.org/10.1186/s12864-017-4083-xopenalex-snapshot
Gapless genome assembly of Colletotrichum higginsianum reveals chromosome structure and association of transposable elements with secondary metabolite gene clusters
inferred← citeshttps://doi.org/10.1186/s12864-018-4440-4openalex-snapshot
Ceratocystis cacaofunesta genome analysis reveals a large expansion of extracellular phosphatidylinositol-specific phospholipase-C genes (PI-PLC)
inferred← citeshttps://doi.org/10.1186/s12864-020-06871-wopenalex-snapshot
Genome compartmentalization predates species divergence in the plant pathogen genus Zymoseptoria
inferred← citeshttps://doi.org/10.1186/s12864-020-06893-4openalex-snapshot
Identification of resistance loci in Chinese and Canadian canola/rapeseed varieties against Leptosphaeria maculans based on genome-wide association studies
inferred← citeshttps://doi.org/10.1186/s12915-021-00989-3openalex-snapshot
Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.1186/s13072-015-0033-5openalex-snapshot
Histone modifications rather than the novel regional centromeres of Zymoseptoria tritici distinguish core and accessory chromosomes
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004227openalex-snapshot
Epigenetic Control of Effector Gene Expression in the Plant Pathogenic Fungus Leptosphaeria maculans
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008272openalex-snapshot
Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009386openalex-snapshot
Genomic rearrangements generate hypervariable mini-chromosomes in host-specific isolates of the blast fungus
inferred← citeshttps://doi.org/10.1371/journal.pone.0103098openalex-snapshot
Genomes and Transcriptomes of Partners in Plant-Fungal- Interactions between Canola (Brassica napus) and Two Leptosphaeria Species
inferred← citeshttps://doi.org/10.1371/journal.ppat.1006241openalex-snapshot
Regulation of proteinaceous effector expression in phytopathogenic fungi
inferred← citeshttps://doi.org/10.14264/uql.2015.627openalex-snapshot
Genome wide identification of NBS-LRR genes in Brassica and their association with disease resistance in Brassica napus
inferred← citeshttps://doi.org/10.14264/uql.2019.886openalex-snapshot
Identification of candidate genes for blackleg resistance in the new Brassica juncea canola
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2017-0161openalex-snapshot
New insights into Phakopsora pachyrhizi infection based on transcriptome analysis in planta
inferred← citeshttps://doi.org/10.18745/th.15117openalex-snapshot
Identification of Avr Alleles in Leptosphaeria maculans Isolates from Different Oilseed Rape Cultivars
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3957992/v1openalex-snapshot
Isolation and identification of blackleg causal pathogen of Chinese cabbage
inferred← citeshttps://doi.org/10.3114/sim.2024.108.01openalex-snapshot
What are the 100 most cited fungal genera?
inferred← citeshttps://doi.org/10.3389/fcell.2022.1072716openalex-snapshot
Comprehending the dynamism of B chromosomes in their journey towards becoming unselfish
inferred← citeshttps://doi.org/10.3389/fgene.2021.727570openalex-snapshot
Evolution of B Chromosomes: From Dispensable Parasitic Chromosomes to Essential Genomic Players
inferred← citeshttps://doi.org/10.3389/fmicb.2016.00600openalex-snapshot
Elucidating the Role of Effectors in Plant-Fungal Interactions: Progress and Challenges
inferred← citeshttps://doi.org/10.3389/fmicb.2018.01005openalex-snapshot
A Dispensable Chromosome Is Required for Virulence in the Hemibiotrophic Plant Pathogen Colletotrichum higginsianum
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01969openalex-snapshot
Generation and Characterization of a Virulent Leptosphaeria maculans Isolate Carrying a Mutated AvrLm7 Gene Using the CRISPR/Cas9 System
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1129319openalex-snapshot
Chromosome-level analysis of the Colletotrichum graminicola genome reveals the unique characteristics of core and minichromosomes
inferred← citeshttps://doi.org/10.3389/fpls.2015.00772openalex-snapshot
Comparative genomic analysis of duplicated homoeologous regions involved in the resistance of Brassica napus to stem canker
inferred← citeshttps://doi.org/10.3389/fpls.2015.00980openalex-snapshot
A Large Family of AvrLm6-like Genes in the Apple and Pear Scab Pathogens, Venturia inaequalis and Venturia pirina
inferred← citeshttps://doi.org/10.3389/fpls.2016.01513openalex-snapshot
Genome-wide Association Study Identifies New Loci for Resistance to Leptosphaeria maculans in Canola
inferred← citeshttps://doi.org/10.3389/fpls.2016.01771openalex-snapshot
Single R Gene Introgression Lines for Accurate Dissection of the Brassica - Leptosphaeria Pathosystem
inferred← citeshttps://doi.org/10.3389/fpls.2016.01784openalex-snapshot
Comparative Transcriptomic Analysis of Virulence Factors in Leptosphaeria maculans during Compatible and Incompatible Interactions with Canola
inferred← citeshttps://doi.org/10.3389/fpls.2017.01788openalex-snapshot
Current Status and Challenges in Identifying Disease Resistance Genes in Brassica napus
inferred← citeshttps://doi.org/10.3389/fpls.2019.00823openalex-snapshot
Transcriptional Insight Into Brassica napus Resistance Genes LepR3 and Rlm2-Mediated Defense Response Against the Leptosphaeria maculans Infection
inferred← citeshttps://doi.org/10.3389/fpls.2021.654604openalex-snapshot
The Rlm13 Gene, a New Player of Brassica napus–Leptosphaeria maculans Interaction Maps on Chromosome C03 in Canola
inferred← citeshttps://doi.org/10.3389/fpls.2021.669997openalex-snapshot
Validating the Strategic Deployment of Blackleg Resistance Gene Groups in Commercial Canola Fields on the Canadian Prairies
inferred← citeshttps://doi.org/10.3390/agronomy14061210openalex-snapshot
Consideration of the Disease Complexes, the Missing Link to Correctly Analyze the Impact of Intercropping on Disease Development
inferred← citeshttps://doi.org/10.3390/agronomy14112682openalex-snapshot
B Chromosomes in Wheat: Evolution, Functions and Breeding Potential
inferred← citeshttps://doi.org/10.3390/biology10080771openalex-snapshot
A Modified Meiotic Recombination in Brassica napus Largely Improves Its Breeding Efficiency
inferred← citeshttps://doi.org/10.3390/cells8020156openalex-snapshot
The Modern View of B Chromosomes Under the Impact of High Scale Omics Analyses
inferred← citeshttps://doi.org/10.3390/genes11060638openalex-snapshot
Polycomb Repression without Bristles: Facultative Heterochromatin and Genome Stability in Fungi
inferred← citeshttps://doi.org/10.3390/ijms19123769openalex-snapshot
Characterization of Callose Deposition and Analysis of the Callose Synthase Gene Family of Brassica napus in Response to Leptosphaeria maculans
inferred← citeshttps://doi.org/10.3390/ijms22010313openalex-snapshot
Recent Findings Unravel Genes and Genetic Factors Underlying Leptosphaeria maculans Resistance in Brassica napus and Its Relatives
inferred← citeshttps://doi.org/10.3390/ijms23073964openalex-snapshot
Leptosphaeria maculans-Brassica napus Battle: A Comparison of Incompatible vs. Compatible Interactions Using Dual RNASeq
inferred← citeshttps://doi.org/10.3390/jof11070514openalex-snapshot
Integrated Management Strategies for Blackleg Disease of Canola Amidst Climate Change Challenges
inferred← citeshttps://doi.org/10.3390/pathogens11040461openalex-snapshot
Efficacy of Blackleg Major Resistance Genes in B. napus in Germany
inferred← citeshttps://doi.org/10.3390/pathogens15090973openalex-snapshot
Previous Viral Infection Triggers Fungal Resistance Breakdown in Host Plants
inferred← citeshttps://doi.org/10.3390/pathogens8040298openalex-snapshot
Repeat-Induced Point Mutations Drive Divergence between Fusarium circinatum and Its Close Relatives
inferred← citeshttps://doi.org/10.3390/plants14030390openalex-snapshot
From Recognition to Response: Resistance–Effector Gene Interactions in the Brassica napus and Leptosphaeria maculans Patho-System
inferred← citeshttps://doi.org/10.3390/plants8110484openalex-snapshot
Effect of Elevated CO2 Concentration on the Disease Severity of Compatible and Incompatible Interactions of Brassica napus–Leptosphaeria maculans Pathosystem
inferred← citeshttps://doi.org/10.3390/plants9050641openalex-snapshot
The Many Questions about Mini Chromosomes in Colletotrichum spp.
inferred← citeshttps://doi.org/10.3410/f.736596519.793576423openalex-snapshot
Faculty Opinions recommendation of Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus.
inferred← citeshttps://doi.org/10.3835/plantgenome2017.11.0100openalex-snapshot
Genomic Prediction Using Prior Quantitative Trait Loci Information Reveals a Large Reservoir of Underutilised Blackleg Resistance in Diverse Canola ( Brassica napus L.) Lines
inferred← citeshttps://doi.org/10.3852/14-317openalex-snapshot
Evolution of virulence in fungal plant pathogens: exploiting fungal genomics to control plant disease
inferred← citeshttps://doi.org/10.53846/goediss-9802openalex-snapshot
Characterization of Leptosphaeria maculans races in Germany and studies on resistance of Brassica napus to blackleg disease
inferred← citeshttps://doi.org/10.5772/53611openalex-snapshot
Genetic Dissection of Blackleg Resistance Loci in Rapeseed (Brassica napus L.)
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274269openalex-snapshot
Additional file 16 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274278openalex-snapshot
Additional file 19 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274281openalex-snapshot
Additional file 1 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274287openalex-snapshot
Additional file 21 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274290openalex-snapshot
Additional file 22 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274293openalex-snapshot
Additional file 23 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274296openalex-snapshot
Additional file 2 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274302openalex-snapshot
Additional file 4 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.6084/m9.figshare.14274308openalex-snapshot
Additional file 6 of Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
inferred← citeshttps://doi.org/10.70675/4aff2f72z5556z4645za684z641686674e34openalex-snapshot
Impact du niveau de ploïdie et de l’évolution des génomes sur le contrôle de la fréquence et de la distribution des évènements de recombinaison chez les Brassicas
inferred← citeshttps://doi.org/10.70675/5e9581e0z8bf8z455bza545z9852f13422bcopenalex-snapshot
Microbial diversity and pathogen-microbiome interactions in crop residues : the case of Zymoseptoria tritici and Leptosphaeria maculans in a wheat-oilseed rape system
inferred← citeshttps://doi.org/10.70675/7d20bd48z8a8az45f9za829z4977a15087a4openalex-snapshot
Génomique comparative et évolutive au sein du complexe d’espèces Leptosphaeria maculans-Leptosphaeria biglobosa
inferred← citeshttps://doi.org/10.70675/86ee747cz89fdz459fz9628za84c27b93555openalex-snapshot
Exploitation du répertoire d’effecteurs de Leptosphaeria maculans pour une diversification des sources de résistance à la nécrose du collet chez Brassica napus
inferred← citeshttps://doi.org/10.70675/91fb6ca0z04acz43f2z9d8dz647e79e1a74dopenalex-snapshot
Incidence des résistances Rlm11 et RlmS du colza sur le microbiote fongique associé à Leptosphaeria maculans et sur la sélection des allèles d'avirulence au cours du cycle infectieux
inferred← citeshttps://doi.org/10.70675/98785856z23ebz4c0bz80e9z9f18344601a3openalex-snapshot
Contrôle chromatinien et transcriptionnel de l'expression des gènes codant des effecteurs chez Leptosphaeria maculans, champignon pathogène du colza
inferred← citeshttps://doi.org/10.70675/a7e6a877zc422z4d7fz9702z75f287ec5f2fopenalex-snapshot
Les modifications des règles de la recombinaison homologue chez les Brassica
inferred← citeshttps://doi.org/10.70675/ae23be89z6d9ez4a77zb907z30aaa63b60a4openalex-snapshot
Dissection transcriptomique de la biologie de Leptosphaeria maculans lors de ses interactions avec son hôte (le colza) et avec un membre du complexe d'espèces, Leptosphaeria biglobosa
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