Epigenetic control of effector gene expression in the plant pathogenic fungus Leptosphaeria maculans

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anglais. Plant pathogens secrete an arsenal of small secreted proteins (SSPs) acting as effectors that modulate host immunity to facilitate infection. In Eukaryotic phytopathogens, SSP-encoding genes are often located in particular genomic environments and show waves of concerted expression at diverse stages of plant infection. To date, little is known about the regulation of their expression. Leptosphaeria maculans is an ascomycete fungus responsible for the most devastating disease of oilseed rape (Brassica napus). The sequencing of its genome revealed a bipartite structure only described so far in higher Eukaryotes, alternating gene rich GC-equilibrated isochores and gene poor AT-isochores made up of mosaics of transposable elements. The AT-isochores encompass one third of the genome and are enriched in putative effector genes that present the same expression pattern (no or a low expression level during in vitro growth and a strong over-expression during primary infection). Here, we investigated the involvement of one histone modification, histone H3 lysine 9 methylation (H3K9me3), in epigenetic regulation of concerted effector gene expression in L. maculans. For this purpose, we silenced expression of two key players in heterochromatin assembly and maintenance, HP1 and DIM5, by RNAi. By using HP1-GFP as a heterochromatin marker, we observed that almost no chromatin condensation is visible in a silenced-dim5 background. Whole genome oligoarrays performed on silenced-hp1 and silenced-dim5 transformants background revealed an over-expression of pathogenicity-related genes during in vitro growth, with a favored influence on SSP-encoding genes in AT-isochores. That increase of expression during in vitro growth was associated with a reduction of H3K9 trimethylation at two SSP-encoding gene loci. The ectopic integration of four effector genes in GC-isochores led to their overexpression during growth in axenic culture. These data strongly suggest that an epigenetic control, mediated by HP1 and DIM5, represses the expression of at least part of the effector genes located in AT-isochores during growth in axenic culture. Our hypothesis is that changes of lifestyle and a switch toward pathogenesis lift chromatin-mediated repression, allowing a rapid response to new environmental conditions.