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Enregistrement W923492831 · doi:10.14264/uql.2015.627

Genome wide identification of NBS-LRR genes in Brassica and their association with disease resistance in Brassica napus

2015· dissertation· en· W923492831 sur OpenAlexaboutno aff
Salman Alamery

Notice bibliographique

RevueThe University of Queensland · 2015
Typedissertation
Langueen
DomaineAgricultural and Biological Sciences
ThématiquePlant-Microbe Interactions and Immunity
Établissements canadiensnon disponible
Organismes subventionnairesnon disponible
Mots-clésBlacklegLeptosphaeria maculansBrassicaCanolaBiologyRapeseedBrassica rapaPlant disease resistancePathosystemGeneGeneticsSyntenyR geneBiotechnologyGenomeBotany

Résumé

récupéré en direct d'OpenAlex

Brassica napus (canola/rapeseed/oilseed rape) is an important commercial oilseed crop in Australia with an annual production of approximately 1.6 million tons of oil. Canola is an important source of edible vegetable oil and has a broad range of industrial purposes. Blackleg disease (stem canker) caused by the fungal pathogen Leptosphaeria maculans, is one of the most devastating diseases in B. napus. This disease causes significant yield losses with an annual average loss of 15 to 48 %, although losses can reach up to 80% worldwide, mainly in Europe, Australia and Canada. In order to develop an effective strategy to control the blackleg disease, there is a need to identify blackleg resistance genes in Brassica species and understand the genetic interaction between plant resistance genes and the pathogen avirulence genes. Thus, identification of Nucleotide Binding Site-Leucine Rich Repeat (NBS-LRR) resistance genes is one of the most important objectives of understanding resistance. NBS-LRR resistance genes have been extensively studied because they represent the largest class of disease resistance genes and play a critical role in defending plants from pathogens. The objective of this study was to perform comprehensive analysis on identification and characterization of NBS-LRR genes in the B. napus genome and to study the synteny and conservation of NBS-LRR genes between Brassica species. In this study, a total of 641, 249 and 443 NBS-LRR encoding genes in B. napus, B. rapa and B. oleracea, respectively, were identified. The comparative analysis between B. napus and its progenitor species indicated that NBS-LRR genes exhibited similar gene structure, genomic location, arrangement in clusters and syntenic relationships. The results provide evidence that there was a selective advantage to maintaining similar features of NBS-LRR genes in B. napus to both B. rapa and B. oleracea following polyploidization. More than 60% of NBS LRR genes from the progenitor species were conserved. The differences in NBS-LRR gene conservation could be attributed to gene losses or selection pressure to offer species-specific or cultivars-specific resistance. This study found that the NBS-LRR resistance genes are physically clustered and individual genes involved in clusters were more polymorphic and subject to evolutionary process than singleton genes. These clusters, which have been described in many other species, provide a reservoir of genetic variation influenced by tandem duplication and selection pressure. In addition, there was a significant correlation and co-localization between the number of NBS-LRR genes within the disease QTL intervals and the number of genes involved in gene clusters or duplication. This correlation provides evidence that NBS-LRR are distributed and clustered throughout the genome and tends to be linked and associated with disease QTL intervals. Genetic studies have identified the gene for gene interactions between avirulence (Avr) genes in L. maculans and their corresponding Rlm (Resistance to Leptosphaeria maculans) genes in B. napus. In addition, genetic mapping studies have shown that there are five major resistance genes on chromosome A7: Rlm1, Rlm3, Rlm4, Rlm7, and Rlm9. At present, none of the genetically mapped Rlm genes on chromosome A7 have been sequenced and validated in B. napus. A total of 12 NBS-LRR and 18 LRR-containing resistance genes were on B. napus chromosome A7 located within the Rlm QTL region of interest. The comparative analysis of these resistance genes between Brassica species confirmed the gene synteny and conservation. However, there was considerable variation; either gene presence/absence or substantial differences in the protein sequence. The comparative analysis allowed making an initial prediction and prioritization for targeting these identified genes for further characterization and validation. In this study, a candidate gene approach, combined with comparative analysis, was exploited for identification of Rlm9 candidate genes in B. napus. The candidate gene approach identified six NBS-LRR and eight LRR-containing genes associated with the Rlm9 QTL region. The NBS-LRR genes were selected for further analysis as highest priority candidate genes. These results provide the first in-depth molecular characterization of NBS-LRR genes in B. napus providing potential candidate gene for disease resistance trait in B. napus. More importantly, this work has significantly increased our understanding about blackleg resistance in B. napus and major disease resistance genes have been identified.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction distillée sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Apprise à partir de 10 348 étiquettes directes de Codex et de 10 348 étiquettes directes de Gemma. Le mode candidate est l'union des têtes enseignantes seuillées; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont ni des étiquettes humaines ni des étiquettes directes de modèles de pointe.

score de la tête « metaresearch » (Codex)0,000
score de la tête « metaresearch » (Gemma)0,000
Version: codex-gemma-dda1882f352aStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Observationnel · Signal consensuel: aucune
GenreSignal candidat: Empirique · Signal consensuel: Empirique
Score de désaccord entre enseignants0,686
Score d'incertitude au seuil0,921

Scores Codex et Gemma par catégorie

CatégorieCodexGemma
Métarecherche0,0000,000
Méta-épidémiologie (sens strict)0,0000,000
Méta-épidémiologie (sens large)0,0000,000
Bibliométrie0,0000,000
Études des sciences et des technologies0,0000,000
Communication savante0,0000,000
Science ouverte0,0000,000
Intégrité de la recherche0,0000,000
Charge utile insuffisante (le modèle a refusé de juger)0,0000,000

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,009
Tête enseignante GPT0,191
Écart entre enseignants0,181 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule tête enseignante, pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeObservationnel
Domainenon disponible
GenreEmpirique

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations3
Publié2015
Routes d'admission1
Résumé présentoui

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