Characterization of siRNAs clusters in <em>Arabidopsis thaliana</em> galls induced by the root-knot nematode <em>Meloidogyne incognita</em>
- Others:
- UMR 1355 ISA ; Institut National de la Recherche Agronomique (INRA)
- COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)
- Institut Sophia Agrobiotech (ISA) ; Institut National de la Recherche Agronomique (INRA)-Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)
- Institut de pharmacologie moléculaire et cellulaire (IPMC) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)
- "Sante des Plantes et Environnement" INRA department; French Government (National Research Agency, ANR) through the 'Investments for the Future' LabEx SIGNALIFE: program [ANR-11-LABX-0028-01]; Plant-KBBE program NESTOR [ANR-13-KBBE-0003-06]; France Genomique National infrastructure as part of "Investissement d'avenir" program [ANR-10-INBS-09]; Provence Alpes Cote d'Azur fellowship
Description
BackgroundRoot-knot nematodes (RKN), genus Meloidogyne, are plant parasitic worms that have the ability to transform root vascular cylinder cells into hypertrophied, multinucleate and metabolically over-active feeding cells. Redifferentiation into feeding cells is the result of a massive transcriptional reprogramming of root cells targeted by RKN. Since RKN are able to induce similar feeding cells in roots of thousands of plant species, these worms are thought to manipulate essential and conserved plant molecular pathways.ResultsSmall non-coding RNAs of uninfected roots and infected root galls induced by M. incognita from Arabidopsis thaliana were sequenced by high throughput sequencing. SiRNA populations were analysed by using the Shortstack algorithm. We identified siRNA clusters that are differentially expressed in infected roots and evidenced an over-representation of the 23-24nt siRNAs in infected tissue. This size corresponds to heterochromatic siRNAs (hc-siRNAs) which are known to regulate expression of transposons and genes at the transcriptional level, mainly by inducing DNA methylation.ConclusionsCorrelation of siRNA clusters expression profile with transcriptomic data identified several protein coding genes that are candidates to be regulated by siRNAs at the transcriptional level by RNA directed DNA methylation (RdDM) pathway either directly or indirectly via silencing of neighbouring transposable elements.
Abstract
International audience
Additional details
- URL
- https://hal.inrae.fr/hal-02628557
- URN
- urn:oai:HAL:hal-02628557v1
- Origin repository
- UNICA