Author:
Sipos György,Prasanna Arun N.,Walther Mathias C.,O’Connor Eoin,Bálint Balázs,Krizsán Krisztina,Kiss Brigitta,Hess Jaqueline,Varga Torda,Slot Jason,Riley Robert,Bóka Bettina,Rigling Daniel,Barry Kerrie,Lee Juna,Mihaltcheva Sirma,Labutti Kurt,Lipzen Anna,Waldron Rose,Moloney Nicola M.,Sperisen Christoph,Kredics László,Vágvölgyi Csaba,Patrigniani Andrea,Fitzpatrick David,Nagy István,Doyle Sean,Anderson James B.,Grigoriev Igor V.,Güldener Ulrich,Münsterkötter Martin,Nagy László G
Abstract
Armillaria species are both devastating forest pathogens and some of the largest terrestrial organisms on Earth. They forage for hosts and achieve immense colony sizes using rhizomorphs, root-like multicellular structures of clonal dispersal. Here, we sequenced and analyzed genomes of four Armillaria species and performed RNA-Seq and quantitative proteomic analysis on seven invasive and reproductive developmental stages of A. ostoyae. Comparison with 22 related fungi revealed a significant genome expansion in Armillaria, affecting several pathogenicity-related genes, lignocellulose degrading enzymes and lineage-specific genes likely involved in rhizomorph development. Rhizomorphs express an evolutionarily young transcriptome that shares features with the transcriptomes of fruiting bodies and vegetative mycelia. Several genes show concomitant upregulation in rhizomorphs and fruiting bodies and shared cis-regulatory signatures in their promoters, providing genetic and regulatory insights into complex multicellularity in fungi. Our results suggest that the evolution of the unique dispersal and pathogenicity mechanisms of Armillaria might have drawn upon ancestral genetic toolkits for wood-decay, morphogenesis and complex multicellularity.
Publisher
Cold Spring Harbor Laboratory