4.7 Article

Transcriptomic Response of Resistant (PI613981-Malus sieversii) and Susceptible (Royal Gala) Genotypes of Apple to Blue Mold (Penicillium expansum) Infection

Journal

FRONTIERS IN PLANT SCIENCE
Volume 8, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fpls.2017.01981

Keywords

malus domestica; Penicillium expansum; qualitative trait loci; postharvest pathogens; wound healing; necrotrophic pathogens

Categories

Funding

  1. BARD from the U.S.-Israel Binational Agricultural Research and Development (BARD) [US-4774-14C]
  2. Spanish Ministry of Economy and Innovation [AGL2011-30519-C03-01, AGL2014-55802-R]
  3. Generalitat Valenciana [PrometeoII/2014/027]

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Malus sieversii from Central Asia is a progenitor of themodern domesticated apple (Malus x domestica). Several accessions of M. sieversii are highly resistant to the postharvest pathogen Penicillium expansum. A previous study identified the qM-Pe3.1 QTL on LG3 for resistance to P. expansum in the mapping population GMAL4593, developed using the resistant accession, M. sieversii -PI613981, and the susceptible cultivar Royal Gala (RG) (M. domestica), as parents. The goal of the present study was to characterize the transcriptomic response of susceptible RG and resistant PI613981 apple fruit to wounding and inoculation with P. expansum using RNA-Seq. Transcriptomic analyses 0-48 h post inoculation suggest a higher basal level of resistance and a more rapid and intense defense response to wounding and wounding plus inoculation with P. expansum in M. sieversii -PI613981 than in RG. Functional analysis showed that ethylene-related genes and genes involved in jasmonate and MYB-domain transcription factor family were over-represented in the resistant genotype. It is suggested that the more rapid response in the resistant genotype (Malus sieversii-PI613981) plays a major role in the resistance response. At least twenty DEGs were mapped to the qM-Pe3.1 QTL (M x d v. 1: 26,848,396-28,424,055) on LG3, and represent potential candidate genes responsible for the observed resistance QTL in M. sieversii-PI613981. RT-qPCR of several of these genes was used to validate the RNA-Seq data and to confirm their higher expression in MSO.

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