Abstract

BackgroundThe filamentous fungus Fusarium graminearum causes devastating crop diseases and produces harmful mycotoxins worldwide. Understanding the complex F. graminearum transcriptional regulatory networks (TRNs) is vital for effective disease management. Reconstructing F. graminearum dynamic TRNs, an NP (non-deterministic polynomial) -hard problem, remains unsolved using commonly adopted reductionist or co-expression based approaches. Multi-omic data such as fungal genomic, transcriptomic data and phenomic data are vital to but so far have been largely isolated and untapped for unraveling phenotype-specific TRNs.ResultsHere for the first time, we harnessed these resources to infer global TRNs for F. graminearum using a Bayesian network based algorithm called “Module Networks”. The inferred TRNs contain 49 regulatory modules that show condition-specific gene regulation. Through a thorough validation based on prior biological knowledge including functional annotations and TF binding site enrichment, our network prediction displayed high accuracy and concordance with existing knowledge. One regulatory module was partially validated using network perturbations caused by Tri6 and Tri10 gene disruptions, as well as using Tri6 Chip-seq data. We then developed a novel computational method to calculate the associations between modules and phenotypes, and identified major module groups regulating different phenotypes. As a result, we identified TRN subnetworks responsible for F. graminearum virulence, sexual reproduction and mycotoxin production, pinpointing phenotype-associated modules and key regulators. Finally, we found a clear compartmentalization of TRN modules in core and lineage-specific genomic regions in F. graminearum, reflecting the evolution of the TRNs in fungal speciation.ConclusionsThis system-level reconstruction of filamentous fungal TRNs provides novel insights into the intricate networks of gene regulation that underlie key processes in F. graminearum pathobiology and offers promise for the development of improved disease control strategies.

Highlights

  • The filamentous fungus Fusarium graminearum causes devastating crop diseases and produces harmful mycotoxins worldwide

  • These two steps were iterated until convergence was reached using the expectation maximization (EM) algorithm, thereby returning the predicted regulatory modules containing a set of regulators and target genes

  • We used a set of candidate regulators consisting of 170 Transcription factor (TF) that were previously functionally associated with key fungal phenotypes available in Fusarium graminearum transcription factor phenotype database (FgTFPD) (Fg TF phenotype database) (Additional file 2) [23]

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Summary

Introduction

The filamentous fungus Fusarium graminearum causes devastating crop diseases and produces harmful mycotoxins worldwide. Understanding the complex F. graminearum transcriptional regulatory networks (TRNs) is vital for effective disease management. Reconstructing F. graminearum dynamic TRNs, an NP (nondeterministic polynomial) -hard problem, remains unsolved using commonly adopted reductionist or co-expression based approaches. Multi-omic data such as fungal genomic, transcriptomic data and phenomic data are vital to but so far have been largely isolated and untapped for unraveling phenotype-specific TRNs. Agricultural plants worldwide commonly suffer from devastating diseases caused by pathogenic fungi [1], threatening food safety and human survival amid increasing global climate change. FHB pathogenesis is tightly controlled by host and pathogen gene regulatory networks (GRNs). GRNs can inform disease control approaches by permitting the specific targeting of key pathogen regulators, as reported in recent studies [8]. GRNs involved in FHB and mycotoxin production remain poorly understood

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