4.5 Article

Identification of lncRNAs Responsive to Infection by Plasmodiophora brassicae in Clubroot-Susceptible and - Resistant Brassica napus Lines Carrying Resistance Introgressed from Rutabaga

Journal

MOLECULAR PLANT-MICROBE INTERACTIONS
Volume 32, Issue 10, Pages 1360-1377

Publisher

AMER PHYTOPATHOLOGICAL SOC
DOI: 10.1094/MPMI-12-18-0341-R

Keywords

canola; clubroot; genomics; long non-coding RNAs; metabolomics; Plasmodiophora brassicae; plant responses to pathogens; primary metabolism; proteomics; RNA-seq

Funding

  1. Alberta Crop Industry Development Fund (ACIDF)
  2. Alberta Canola Producers Commission (ACPC)
  3. Agriculture and Agri-Food Canada
  4. Natural Sciences and Engineering Research Council of Canada

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Clubroot disease, caused by Plasmodiophora brassicae Woronin, is a major threat to the production of Brassica' crops. Resistance to different P. brassicae pathotypes has been reported in the A genome, chromosome A08; however, the molecular mechanism of this resistance, especially the involvement of long noncoding RNAs (lncRNAs), is not understood. We have used a strand-specific lncRNA-Seq approach to catalog lncRNAs from the roots of clubroot-susceptible and - resistant Brassica napus lines. In total, 530 differentially expressed (DE) lncRNAs were identified, including 88% of long intergenic RNAs and 11% natural antisense transcripts. Sixteen lncRNAs were identified as target mimics of the microRNAs (miRNAs) and eight were identified as the precursors of miRNAs. KEGG pathway analysis of the DE lncRNAs showed that the cis-regulated target genes mostly belong to the phenylpropanoid biosynthetic pathway (15%) and plant-pathogen interactions (15%) while the transregulated target genes mostly belong to carbon (18%) and amino acid biosynthesis pathway (19%). In all, 24 DE lncRNAs were identified from chromosome A08, which is known to harbor a quantitative trait locus conferring resistance to different P. brassicae pathotypes; however, eight of these lncRNAs showed expression only in the resistant plants. These results could form the basis for future studies aimed at delineating the roles of lncRNAs in plant-microbe interactions.

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