Literature DB >> 28050618

Clubroot resistance QTL are modulated by nitrogen input in Brassica napus.

A Laperche1, Y Aigu1, M Jubault1, M Ollier1, S Guichard1, P Glory1, S E Strelkov2, A Gravot1, M J Manzanares-Dauleux3.   

Abstract

KEY MESSAGE: Nitrogen levels can modulate the effectiveness of clubroot resistance in an isolate- and host-specific manner. While the same QTL were detected under high and low nitrogen, their effects were altered. Clubroot, caused by Plasmodiophora brassicae, is one of the most damaging diseases of oilseed rape and is known to be affected by nitrogen fertilization. However, the genetic factors involved in clubroot resistance have not been characterized under nitrogen-limiting conditions. This study aimed to assess the variability of clubroot resistance under different nitrogen levels and to characterize the impact of nitrogen supply on genetic resistance factors. Linkage analyses and a genome-wide association study were conducted to detect QTL for clubroot resistance and evaluate their sensitivity to nitrogen. The clubroot response of a set of 92 diverse oilseed rape accessions and 108 lines derived from a cross between 'Darmor-bzh' (resistant) and 'Yudal' (susceptible) was studied in the greenhouse under high- and low-nitrogen conditions, following inoculation with the P. brassicae isolates eH and K92-16. Resistance to each isolate was controlled by a major QTL and a few small-effects QTL. While the same QTL were detected under both high and low nitrogen, their effects were altered. Clubroot resistance to isolate eH, but not K92-16, was greater under a low-N supply versus a high-N supply. New sources of resistance were found among the oilseed rape accessions under both low and high-N conditions. The results are discussed relative to the literature and from a crop improvement perspective.

Entities:  

Keywords:  Abiotic and biotic stresses; Genetic diversity; Linkage and GWAS analyses; Multi-stress; Oilseed rape; Plasmodiophora brassicae

Mesh:

Substances:

Year:  2017        PMID: 28050618     DOI: 10.1007/s00122-016-2842-8

Source DB:  PubMed          Journal:  Theor Appl Genet        ISSN: 0040-5752            Impact factor:   5.699


  28 in total

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Journal:  Theor Appl Genet       Date:  2016-06-30       Impact factor: 5.699

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