Abstract

BackgroundSmall RNAs are short non-coding RNAs that are key gene regulators controlling various biological processes in eukaryotes. Plants may regulate discrete sets of sRNAs in response to pathogen attack. Sclerotinia sclerotiorum is an economically important pathogen affecting hundreds of plant species, including the economically important oilseed B. napus. However, there are limited studies on how regulation of sRNAs occurs in the S. sclerotiorum and B. napus pathosystem.ResultsWe identified different classes of sRNAs from B. napus using high throughput sequencing of replicated mock and infected samples at 24 h post-inoculation (HPI). Overall, 3999 sRNA loci were highly expressed, of which 730 were significantly upregulated during infection. These 730 up-regulated sRNAs targeted 64 genes, including disease resistance proteins and transcriptional regulators. A total of 73 conserved miRNA families were identified in our dataset. Degradome sequencing identified 2124 cleaved mRNA products from these miRNAs from combined mock and infected samples. Among these, 50 genes were specific to infection. Altogether, 20 conserved miRNAs were differentially expressed and 8 transcripts were cleaved by the differentially expressed miRNAs miR159, miR5139, and miR390, suggesting they may have a role in the S. sclerotiorum response. A miR1885-triggered disease resistance gene-derived secondary sRNA locus was also identified and verified with degradome sequencing. We also found further evidence for silencing of a plant immunity related ethylene response factor gene by a novel sRNA using 5′-RACE and RT-qPCR.ConclusionsThe findings in this study expand the framework for understanding the molecular mechanisms of the S. sclerotiorum and B. napus pathosystem at the sRNA level.

Highlights

  • Small RNAs are short non-coding RNAs that are key gene regulators controlling various biological processes in eukaryotes

  • Overview of sequencing results To determine the role of B. napus Small RNA (sRNA) during S. sclerotiorum infection we sequenced six sRNA libraries on the Illumina platform from three replicates each of mock and infected samples at 24 h post-inoculation (HPI) when Sclerotinia stem rot (SSR) symptoms manifested on leaves

  • We identified different classes of sRNAs in B. napus plants that responded to infection with S. sclerotiorum and showed how they may be involved in regulating different sets of genes using degradome sequencing

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Summary

Introduction

Small RNAs are short non-coding RNAs that are key gene regulators controlling various biological processes in eukaryotes. Small RNAs (sRNAs) are short non-coding RNAs, ranging in size from 18 to 30 nucleotides (nt), that are important for gene expression regulation and genome stability in eukaryotes [1]. There are three major sRNA sRNAs in plants silence gene expression through the RNA interference (RNAi) pathway. RNA dependent RNA polymerases (RdRps), Dicer-like proteins (DCLs), and Argonauts (AGOs) are the main RNAi pathway enzymes. Regmi et al BMC Plant Biology (2021) 21:366 are processed into sRNAs by DCLs. In general, AGO is thought to guide one of the strands (the guide strand) of dicer-processed sRNAs to silence complementary targets [4] while the other strand (the passenger ‘sRNA*’ strand), is often quickly degraded. In addition to complementary pairing with transcripts, siRNAs can regulate gene expression epigenetically by RNA-directed methylation of complementary DNA [1]

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